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Multifunctional carbon-based nanomaterials offer routes towards the realization of smart and high-performing (opto)electronic (nano)devices, sensors and logic gates. Meanwhile photochromic molecules exhibit reversible transformation between two forms, induced by the absorption of electromagnetic radiation. By combining carbon-based nanomaterials with photochromic molecules, one can achieve reversible changes in geometrical structure, electronic properties and nanoscale mechanics triggering by light. This thus enables a reversible modulation of numerous physical and chemical properties of the carbon-based nanomaterials towards the fabrication of cognitive devices. This review examines the state of the art with respect to these responsive materials, and seeks to identify future directions for investigation.
Carbon is the fourth most abundant element in the universe by mass and it forms a vast number of compounds, more than any other chemical element. It assembles into several allotropes that hold extraordinary yet markedly different chemical and physical properties1,2,3,4,5,6,7, including their structure and geometry, optical, mechanical, electrical/electronic properties and stability, making them key building blocks for numerous applications in materials science and nanotechnology8,9,10,11,12,13,14,15,16,17,18. A common characteristic of fullerene, carbon nanodots, carbon nanotubes (CNTs) and graphene (including large polycyclic aromatic hydrocarbons) is the ability to functionalize them covalently and non-covalently with specific moieties, thereby improving their solubility in liquid media and imparting them with enhanced/additional properties. Among various moieties, the functionalization of carbon-based systems with building blocks that can respond to external stimuli enables the generation of smart/dynamic carbon-based nanomaterials, by offering additional remote controls (for example, light, mechanical pressure, pH, electric/magnetic fields and so on) to modulate their properties19,20,21. Among various stimuli, light is a perfect choice since it features high spatio-temporal resolution and it is non-invasive over a wide range of wavelengths. Furthermore, the possibility to tune their wavelength and intensity guarantees a wealth of solutions when the photochromic systems are intelligently designed.
Photochromic molecules can undergo reversible photo-triggered isomerization between (at least) two (meta)stable states. Hitherto, a variety of photochromic molecules have been designed and synthesized, using not only E/Z isomerization, but also valence isomerization, cycloadditions, tautomerizations and so on. Depending on the type of chemical processes involved, photochromic molecules can generally be divided into several classes22: (1) pericyclic reactions including electrocyclizations like spiropyrans/-oxazines, fulgides and diarylethenes, or cycloadditions in aromatic compounds; (2) E/Z isomerizations such as azobenzenes, stilbenes and so on; (3) intramolecular hydrogen/group transfer such as anils and polycyclic quinones; (4) photo-induced bond cleavages such as triarylmethanes and perchlorotoluene; (5) electron transfers (redox) such as viologens. Among all photochromic molecules, the most widely used are azobenzenes23, diarylethenes24, spiropyrans/-oxazines25 and stilbenes26. Among these four, diarylethenes can be switched between the two states photochemically or electrochemically, whereas the other three molecules can be reverted either photochemically or thermally (Fig. 1). The basic properties of the above mentioned photochromic molecules are summarized in Table 1. The switching behaviour, including rate of the isomerization and stability of the different isomers, depends on several factors such as their surrounding environment, substituents and so on.
The functionalization of carbon-based nanomaterials with photochromic moieties is a widely exploited approach to confer them the capacity to respond to light stimuli at specific wavelengths. The photochromic system's isomers possess markedly different properties at the single molecule level which give rise to remarkably diverse macroscopic properties, that is, at the ensemble level27,28,29,30. Therefore, the decoration of carbon-based nanomaterials with photochromic molecules to control local variation in the optical, mechanical, electrostatic environment via a light input has sparked great interest in the community of chemistry, physics and materials science. The combination of photochromic molecules with carbon-based nanomaterials is therefore being pursued to develop bi- or multi-functional molecular materials: the hybrid system will not only possess the unique properties of each component, but shall also feature the emergence of new properties that can potentially be used for specific applications. In this review, we provide a critical literature survey on the most enlightening results reported on carbon-based nanomaterials functionalized with photochromic molecules with a particular focus on the functionalization methods, on the dynamic properties conferred to the materials and their applications when integrated in working devices. The potential of these smart materials for the generation of novel, multifunctional, low-cost, large-area and flexible devices is discussed.
Functionalization of carbon-based nanomaterials such as fullerene, carbon nanodots, CNTs, graphene (including large polycyclic aromatic hydrocarbons) with molecular moieties possessing suitable properties is essential for the realization of new molecular hybrid materials with novel/enhanced functions. Regiospecific substitutions of carbon-based nanomaterials with functional groups in the scaffold and/or in the periphery is a viable approach to improve their stability, dispersibility thus processiblility, and provide tools to introduce new functions that can be used to further tune their properties. Functionalization of carbon-based nanomaterials with photochromic molecules including azobenzenes, diarylethenes, spiropyrans/-oxazines, and stilbenes can be achieved either through non-covalent31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46 or covalent approaches47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69. On the one hand, non-covalent modification of carbon-based nanomaterials is typically based on physical adsorption of photochromic units on carbon nanomaterials via π–π stacking, hydrophobic interaction or electrostatic interaction; such a strategy is advantageous since it only mildly perturbs the sp2 structure of the carbon allotrope, thus it is a viable method to adjust the properties of carbon-based nanomaterials via electronic communications. Because of these reasons, non-covalent functionalization has been widely used to build carbon-based functional optoelectronic devices. Pyrene unit is being frequently employed as an anchoring group for non-covalent functionalization of carbon-based nanomaterials with photochromic molecules35,36,37,38,39,40. On the other hand, covalent functionalization between carbon-based nanomaterials and photochromic molecules via condensation reactions (amidation48,49,50,51,52,53,54,55,56 or ester formation57,58,59), cycloaddition60,61,62, click chemistry63, diazonium chemistry64,65 and radical polymerization66,67,68 and so on69, enables strong and robust bonding and can offer a control over the degree of functionalization (Fig. 2). In terms of covalent functionalization, one common and convenient approach is to oxidize carbon atoms to generate carboxylic groups, which can be subjected to further functionalization via condensation reactions48,49,50,51,52,53,54,55,56,57,58,59. The degree of functionalization of carbon-based nanomaterials with photochromic molecules can be determined using thermal gravimetric analysis and X-ray photoelectron spectroscopy. It reveals that for every dozens to several hundreds of carbon atoms in the carbon-based core, there is one photochromic moiety appended, depending on the chemistry and conditions employed51,53.
Due to the responsive nature of photochromic molecules, light can be used as an external remote control to reversibly regulate the properties of carbon-based materials and devices. Changes at the single-molecule level such as geometry/conformation, electronic structure, dipole moment, redox potential, can result in remarkably diverse properties at the materials level including shape70, aggregation behaviour34, conductance21, magnetism71, fluorescence55,68 and so on72. Examples of modulation the properties of photochromic carbon-based nanomaterials are summarized in Table 2. The modulation of the properties not only depends on the photochromic molecules and carbon-based materials employed, but it is also affected by the interactions between the two components, the measurement conditions and so on. For example, modulation of the properties of graphene using photochromic molecules depends on the type of graphene used (reduced graphene oxide (rGO) versus mechanical exfoliated graphene versus graphene grown by chemical vapour deposition); there is a dramatic difference in the modulation range of dipole moment between using azobenzenes and spiropyrans, which can affect the charge transport properties in the hybrid materials. Compared with alkyl substituted photochromic molecules, pyrene-substituted ones interact differently with carbon-based nanomaterials, which will affect the experimental results; the distance between photochromic molecules and carbon-based nanomaterials also plays an important role in the interactions. Other factors like irradiation time, solvents used or level of vacuum also contribute to the final performance of the hybrid systems.
Among the various properties, a subtle control over the energy level alignments of the different components/moieties enables the use of light to control electronic cross-talking between different units in a multicomponent material leading to the modulation of fundamental optoelectronic processes such as charge generation, transfer and recombination as well as energy transfer73,74,75,76,77,78, which are ruling the operation of light-emitting diodes, organic solar cells, artificial photosynthetic systems and single-molecule devices. The type of chosen photochromic molecules and carbon-based nanomaterials as well as the chemical nature of the linker will define the charge transfer/separation processes between them, thereby influencing the efficiency of the photochromic system (for example, time response to the external stimuli, lifetime of the isomers, fatigue resistance and so on). For example, photo-induced geometrical/structural changes of photochromic molecules or changes of the length/structure of the linkers can be used to regulate the distance/conjugation between the two components, thus can modulate the efficiency of electron and/or energy transfer processes. On the other hand, the widespread use of fluorescence together with the need to further understand how to design and control the photophysical properties of functional (nano)materials have stimulated the identification of mechanisms to reversibly switch the emission of these (nano)materials with external stimuli31. In particular, strategies to reversibly modulate the fluorescence of carbon-based nanomaterials using light have already been developed successfully based on electron and/or energy transfer processes55,68, which might lead to novel photonic materials for information technology as well as luminescent probes for biological applications. The packing and orientation of photochromic molecules in carbon-based nanomaterials can be also altered by light, resulting in changes in conformation/structure to be used as molecular machines, actuators or sensors. By controlling the irradiation time, intensity and spot location, light can be very easily utilized to tune the degree of modification of the target function to realize multiscale responsive carbon-based nanomaterials controlled both in time and space, for example, as a viable approach to fabricate multilevel non-volatile optical memories.
The ability to modulate the functions of (nano)devices using external stimuli is highly desirable in microelectronics, nanoelectronics and especially in optoelectronics due to their potential applications in switching, sensing, memories and so on. In view of their outstanding light responsive nature, photochromic carbon-based nanomaterials are particularly suitable for these broad applications. Here we discuss recent progresses on the integration of photochromic carbon-based nanomaterials as components in nanodevices (for example, as molecular junctions79,80,81,82,83,84,85,86,87,88, as electroactive-species in field-effect transistors (FETs)89,90,91,92,93,94,95,96,97,98), and optoelectronic devices (for example, optical read-out99, optical memories42, color detector100, and solar thermal fuels20). Alongside, their application in sensing100, including biomedical imaging and drug delivery52 will be also highlighted. Photochromic molecules whose isomers exhibit remarkably different properties, when combined with carbon-based nanomaterials, are also potentially useful to fabricate smart/dynamic (nano)materials (for example, smart nanocomposites/windows/labels)27. Towards multifunctional materials, in addition to the integration of photochromic systems that can respond to a light input, carbon-based nanomaterials can be decorated with functional groups that respond to other stimuli like pH and/or electric fields. The read-out can occur optically or electrically.
The electrical characteristics of photochromic molecules can be explored by embedding them in-between two electrodes in a molecular junction. Molecular junctions rely on nanoscopic or macroscopic electrodes whose geometry and spacing can enable the measurement of the transport through single molecules. Because of its fundamental quantum-mechanical nature, charge transport through molecular junctions is an exciting field, at the cross-road between mesoscopic physics, quantum computing and spintronics.
Being the switch, a key element in (nano)electronics, the ability of gating the conductance of a single molecule using an external remote control has a paramount importance. The electrical characteristic of an electrode–molecule–electrode junction is governed by the structure and energetics of the two components and their interfaces, as well as by the ability of the chosen molecule to transport charges. The former requires to achieve a high-structural control over the electrode surface and its combination with functional groups attached in the periphery of the molecule to guarantee precise (non)covalent linkage79. Compared with other electrode materials like metals, carbon-based materials possess obvious advantages, such as extraordinary and modulable electronic properties, natural compatibility with molecules to enable more stable contacts. Bridging carbon-based electrodes with photochromic molecules is a viable route towards conferring an optical response to an electronic device.
Cuniberti and co-workers21 reported a theoretical investigation on the charge transport of a prototypical junction consisting of single azobenzene molecule connecting two CNT electrodes. They showed that the low energy conduction properties of the junction may be drastically modified by changing the topology of the contacts between the CNTs and the photochromic molecule, and/or the chirality of the CNTs. Later on, several theoretical studies on the combination of photochromic molecules with CNTs/graphene have been carried out80,81. The conductivities were found to be significantly different for the two photochromic isomers. All these theoretical studies have triggered an experimental effort and contributed to the understanding of the experimental results.
Contacting a single molecule with two symmetric electrodes is not a trivial task. Importantly, the spacing between adjacent electrodes needs to match exactly the size of the molecule. Nuckolls and co-workers82 reported an experimental work that relied on the bridging of two CNTs with a diarylethene molecule via amide formation. The CNTs point contacts were made by electron beam lithography. In their system, two different diaryethene molecules were used (Fig. 3a). When X=S, the thiophene-based devices show only one-way switching from open to closed state, changing from a lower conductance state to a higher conductance state. When X=NMe, the pyrrole-based devices can be switched on/off for several times. They hypothesized that the CNT electrode dissipates the energy generated in the excited-state of the closed form of thiophene-based diarylethene (X=S). These results highlight the importance of molecular structures, which drastically affect the device characteristics and its final performance. If the electronic coupling between the electrode and the photochromic molecule is sufficiently strong, on irradiation with light, either electron or hole may leak out to the electrodes on a timescale shorter than the time needed for the photochrome to switch, which will result in the loss in the photochromic functionality.
Single-molecule junctions based on the wiring of graphene electrodes with diarylethene have also been reported83. Graphene point contacts arrays with narrow gaps were patterned by a dashed-line lithography process with carboxylic acid terminal groups, which can react with diarylethene bridges derivatized with amino moieties via amide tethering. Under ultraviolet light irradiation, the devices show a photo-switching behaviour from low-conductance state to high-conductance state, which is due to the ring closing of the diarylethene generating a conjugated pathway for charges travelling from one graphene electrode to the other. However, as a result of the quenching induced by the strong coupling between diaryethenes and graphene electrodes, the devices cannot isomerize back to the low-conductance state. By using a similar approach, the same group was able to achieve a reversible conductance switching of azobenzene units covalently connecting to two graphene point contacts on device exposure to external light (Fig. 3b)84. Owing to the presence of two sulfonic acid groups in the azobenzene molecule, the conductance of the device is also sensitive to pH stimuli. It is worth mentioning that the conductance changed more than two orders of magnitude from acid to basic condition, thus providing an ultrasensitive local probe for monitoring pH changes based on single molecules. This study represents a good example of designing multifunctional single molecular devices towards the construction of logic gates or even molecular computers. Although the above symmetric junctions consisting of two CNTs or graphene-based electrodes showed promising results, bridging the interelectrodic gap with an atomic precision using single molecules remains a major challenge.
Vertical junctions incorporating photochromic molecules have been also realized and characterized. A photo-switchable self-assembled molecular monolayer (SAM) of thiol-substituted dihydroazulenes has been sandwiched between a gold electrode and an ultrathin thermally rGO film acting as transparent top contact, allowing in situ illumination to attain photo switching; optical–thermal stimuli was therefore employed to run the device85. Reversible conformational change between dihydroazulenes and vinylheptafulvene was triggered by alternating light irradiation and heat treatment, with an average Ion/Ioff ratio of 5–7. This Ion/Ioff ratio is smaller than the one determined in the molecular junction incorporating photoactive azobenene or diarylethene82,84,87. In this case, rGO was chosen because of its high transparency, good conductivity and flexibility, solution processability, excellent chemical stability and molecular compatibility. Lee and colleagues86 independently developed a method to fabricate flexible and photo-switchable vertical junctions using graphene as electrodes. In their approach, azobenzenes were covalently attached to the graphene bottom electrode via diazonium chemistry so as to prevent the local movement of photo-switchable molecules, while the other side of the azobenzenes is physically contacted to the graphene top electrode. The graphene electrodes were prepared by a chemical vapour deposition method, which yields higher conductivity compared with rGO films. The as-fabricated devices are stable under severe mechanical stress and for a large number of photo-switching cycles with an Ion/Ioff ratio ~13, suggesting the potential application in flexible switching devices.
More recently, a graphene/azobenzene/Au heterostructure was designed by Margapoti et al.87. In this case, a mixed SAM of an azobenzene derivative and a spacer molecule has been co-adsorbed, the latter component allowing to prevent steric hindrance of the photo-induced conformational switching and intermolecular coupling of the azobenzene. The strength of the current resonances determined by conductive atomic force microscopy can be reversibly gated optically with an Ion/Ioff ratio exceeding 100; such a switch was found to further induce the reversible modification of the electrical and quantum properties of the Dirac fermions of graphene. In a previous report by our group together with Mayor101, a conductive atomic force microscopy tip/azobenzene/Au junction was devised, without the use of graphene and a spacer molecule, and it revealed a 30-fold increase in conductance as a result of the conformational change of azobenzene in a process ruled by tunnelling. The change in conductance is smaller than the one reported for graphene/azobenzene/Au junctions. Devices with a rGO/diarylethene/Au heterostructure on a flexible substrate have also been fabricated88, showing a reversible conductance change in response to alternating irradiation with ultraviolet/visible light. In addition, the switchable devices show good longtime stability under various mechanical deformations.
Compared with CNTs, an obvious advantage of graphene as an electrode material lies in the fact that it does not have the inherently variable diameter and chirality, which should rule out the possibility of modulating the junction conductance by the electrode chirality as it has happened in CNTs. Compared with electrodes using rGO and graphene prepared via chemical vapour deposition, the advantage of the former lies in its solution processability while the latter retains the intrinsic exceptional properties of graphene.
While molecular junctions are essential to gain insight into the possibility of transporting charges through single molecules, their technological relevance is limited because of the excessive costs associated to the scaling down lithographic procedures. However, the information gathered on the charge transport through single molecules is instrumental towards the development of high-performance macroscopic devices. In this regard, FETs, which are the key element of microelectronics, are mono-functional devices that rely on the electrical gating to modulate transport of one type of charge carrier in a semiconducting material. The integration of a photo-responsive molecule in a transistor allows to develop a bi-functional device, that is, a device which is capable of responding to two independent stimuli. Because of this reason one of the most worthwhile application of photochromic carbon-based nanomaterials is their use as electroactive-species in FETs. One practical way to combine electrically (semi)conducting materials with photochromic systems is by means of non-covalent interactions. The functionalization of CNTs with spiropyrans was demonstrated by Nuckolls and co-workers89. In their study, spiropyrans derivatized with either alkane or pyrene groups were physisorbed on CNTs (Fig. 3c). For spiropyrans, the charge-separated ring-opened, coloured form named merocyanine is generated by irradiation with ultraviolet light, whereas the reversing ring closure is triggered with visible light to form the neutral, colourless form. Such a reversible photo-isomerization process causes a significant change in the dipole moment, which could initiate a significant modification in the electrostatic environment. FETs based on these spiropyran functionalized CNTs could be switched from high to low-conductance state as the spiropyrans photo-isomerized from the open to the closed state. The merocyanines acted as scattering sites and/or charge traps, leading to a decrease in conductance. These devices can detect the photo-switching events of ~104 molecules. This study represents a good example of combining microfabrication with self-assembly of photo-responsive molecules towards functional FETs. Using a similar approach, azobenzenes with an anthracene anchoring group were physisorbed on CNTs90. When azobenzene undergo photo-isomerization from the Z to the E form, the resulting change in dipole moment modifies the local electrostatic potential and modulates the transistor conductance by shifting the threshold voltage. A shift in the threshold voltage of up to 1.2V was observed at a degree of functionalization of ~1–2 azobenzene molecules every 100 carbon atoms. Importantly, the conductance change was reversible and repeatable for a long period of time, with a modest of ~2s switching time.
Similar strategies have also been applied to realize graphene-based transistors. In this framework, Gopalan and co-workers91 reported light-driven reversible doping of graphene by pyrene-substituted azobenzenes. The charge carrier concentration could be modulated by ~±1 × 1012cm−2 by ultraviolet and white light illumination, meanwhile preserving charge carrier mobilities of pristine graphene. Compared with substitutional doping, the retention of high mobilities, the ability to reversibly modulate doping using light and the ease of processing are clear advantages of this study91. Peimyoo et al. studied the doping of azobenzenes without pyrene groups directly deposited on graphene92. The E form modified graphene shows stronger doping effect than that of Z form due to the molecular conformation change (charge carrier concentration from ~5 × 1013 to ~4 × 1013cm−2), which has different interactions with graphene. Using a similar strategy, our group together with M. Mayor reported the modification of the source and drain Au electrodes of an organic FET with a thiolated biphenyl azobenzene SAM102. The semiconductor was located in the transistor channel. The current in the as-fabricated device can be reversibly modulated by 20%, which is attributed to the photochemical modulation of the tunnelling barrier for injection/extraction of charges from the electrodes into the organic semiconductor. Conversely, in the above examples of azobenzene modified carbon-based FETs, the azobenzene molecules were directly deposited on the top of CNT/graphene90,92,93.
In a later report, reversible light-modulated doping of graphene using pyrene-substituted spiropyrans was also described94,95. Changes in Dirac point and mobility are reversible via alternating ultraviolet and visible light irradiation, and the doping level of graphene functionalized with spiropyrans can be controlled. The hole and electron mobility of the functionalized graphene with spiropyrans after ultraviolet irradiation slightly decreased to 508.8 to 392.4cm2V−1s−1, and from 428.4 to 301.2cm2V−1s−1, respectively (Fig. 3d)94, a result that has been attributed to charge scattering. The electrical conductivity of a photochromic blend composed of polymers having diarylethene derivatives in the main chain and CNTs as active components in transistors is reversibly tuned on cycling ultraviolet and visible light96. The photo-switching capacities of the diarylethene in the main chain of the polymer observed in solution are retained on physisorption on the CNT surface. Based on electrical and spectroscopic evidence, the authors concluded that the intertube electrical coupling, mediated by the light-induced electrocyclization of the switch, is responsible for the conductivity modulation of the device.
As alternative strategy to the above non-covalent functionalization approach, azobenzenes were covalently tethered onto chemically rGO sheets, whose carrier density can be modulated reversibly via light irradiation97. A change in dipole moment from E to Z leads to the generation of a high effective gating voltage. All these examples of ‘light-modulated' transistors open up new pathways towards the generation of optical interconnects and light-addressable logic circuits.
Solar energy conversion and storage are one of the key challenges in modern society. Among them, effective conversion of light into heat is an emerging area showing great potential for a number of applications, such as in solar thermal storage. Solar thermal fuels can store energy from light in photochromic molecule's isomerization process, with their metastable forms capable of releasing nearly 100% of the stored energy as heat as the result of external stimuli along with the reversion to the stable forms. Solar thermal fuels are regarded as a closed-cycle system that only transfers energy from and to the environment by reversible transformation20. However, solar thermal storage is still hindered by a low storage capacity, short-time storage and lack of novel designed structures. Recently, novel hybrid solar thermal fuels have been prepared through covalent linkage of CNTs with azobenzenes, as demonstrated both theoretically and experimentally by Grossman and co-workers20,103,104. Azobenzene undergoes a conformational change under ultraviolet light irradiation from E to a higher energy metastable Z form, thus storing energy ΔH. To recover the stored energy, an external trigger is applied to overcome the thermal barrier Ea, thus releasing a net energy of ΔH in the form of heat per azobenzene molecule (Fig. 4a). In the system, CNTs not only acts a template for packing and orientation of the tethered azobenzene molecules, but also have a significant effect on the energetics of the system by breaking the symmetry of the azobenzene molecules. A relatively low energy density of 56Whkg−1 was obtained due to the low packing densities of azobenzene attached onto CNTs through radical chemistry (one azobenzene every 18.2 carbon atoms, see Fig. 4b for the chemical structure of the hybrid)20. The condensation of the hybrid materials in the solid-state by solvent removal to form a more close-packed arrangement led to twofold enhancement of the storage energy capacity. The selection of the carbon-based templates and the orientation of the photochromic molecules can also affect the final performance of the devices. Using a different chemical approach, azobenzenes were also chemically attached onto rGO via diazonium chemistry for long-term solar thermal storage by Feng's group105,106,107. Optimizing intermolecular hydrogen bonding interactions and also increasing the functionalization degree (up to one azobenzene every 17 carbon atoms) can remarkably improve both the storage capacity and lifetime, showing an energy density up to 138Whkg−1, a long-term storage half-life exceeding 1 month and excellent cycle stability for 50 cycles107. However, the packing density of azobenzene in the above hybrid systems is still far beyond the optimized value predicted by theory (i.e., one azobenzene every eight carbon atoms)103,104, suggesting that new chemical approaches need to be devised to improve the degree of functionalization in carbon-based templates using photochromic molecules.
With the development of information technology, there is a high demand to exploit new methods for data storage. In this framework, the maximization of the data storage densities is a major goal in memory devices. This can be achieved by developing all-optical switching devices that exhibit high switching rates or multilevel storage. An ideal memory device should be stable, easy to write, read and erasable. Photochromic molecules that change their state reversibly in response to external stimuli could be used to build non-volatile memory devices: their data storage capacity allows writing and erasing data in photon mode with a high spatial and temporal resolution. Carbon-based nanomaterials, and especially graphene, are excellent candidates as electrodes in memory devices due to their unique properties such as high conductivity, transparency and good flexibility. Memory devices consisting of photochromic molecules as an active layer sandwiched between two graphene electrodes have been developed. As a typical example, Min et al.108 reported the fabrication of voltage-controlled non-volatile molecular memory devices by using an azobenzene monolayer as the active layer incorporated between two chemically rGO films acting as electrodes via an all-solution-processed approach (Fig. 4c). First, a graphene oxide film was spin-coated onto an indium tin oxide coated plastic substrate, followed by a hydrazine vapour reduction step to obtain the rGO film, which was then used as the bottom electrode. In the second step, a monolayer of azobenzene was chemically attached onto the rGO film via diazonium chemistry. Finally, a device with a configuration of rGO/azobenzene monolayer/rGO was obtained by spray-coating of rGO solution as the top electrode. The as-fabricated devices showed a typical rewritable memory behaviour with an Ion/Ioff ratio of 20 and a retention time exceeding 104s (Fig. 4c), which is due to the resistive switching of the azobenzene monolayer (while the control device incorporating only rGO did not show any memory effect). The non-volatile memory exhibited a stability exceeding 400 cycles of write–read–erase–read. Interestingly, these devices also showed good memory characteristics under bending stress, demonstrating their potential use in flexible electronic devices. However, the influence of the degree of reduction of rGO on the device performance is yet to be studied. Optical controlled graphene-based non-volatile ternary-logic memory with azobenzene copolymer as an active layer was also demonstrated109. In this case, mechanical cleavage graphene was used as the bottom electrode and indium tin oxide was employed as the top electrode. The graphene-based devices can perform ternary logic, and the resistance change ratio of the written status ‘±1' to the erased status ‘0' was 60%. Instead of using azobenzenes, diarylethenes would be a more suitable candidate for memories devices due to its bistable nature and excellent fatigue resistance. Furthermore, improving the reproducibility from device to device and a better understanding of the memory mechanism should be further explored.
Each constituting atom of CNTs and graphene is exposed to the environment. Because of this reason these nanostructures are extremely sensitive to environment modification at the nanoscale, thus they are ideal platforms for sensing. Photochromic carbon-based nanomaterials are a class of promising sensors due to the intrinsic isomerization and colorimetric/fluorescent properties. To date, sensitivity and selectivity of sensors based on photochromic carbon-based nanomaterials are major features that need to be harnessed. This may be achieved via the decoration of the building block with units that can selectively recognize the molecules to be sensed via specific interactions. Via rational design of photochromic carbon-based nanomaterials, it should be possible to achieve visual, sensitive and high-throughput detection.
Zhou et al.100 reported a nanoscale color detector based on CNTs modified with azobenzenes, where the azobenzenes serve as photo-absorbers and the nanotube as the electronic read-out (Fig. 5a). By synthesizing azobenzenes with specific absorption windows in the visible region and anchoring them to the nanotube surface via pyrene linker group, they demonstrated the controlled detection of visible light of low intensity in narrow ranges of wavelengths. The authors suggest that on photoexcitation, azobenzenes undergo isomerization from the E state to the Z state, accompanied by a large change in dipole moment, therefore, modifying the electrostatic environment of the nanotube. The calculated values of the dipole moments support the notion of dipole changes as the optical detection mechanism. This system can be used to study fundamental properties of chromophore–nanotube hybrids and to probe molecular transitions. This approach represents a useful way to make colour photodetectors with nanoscale resolution.
Qu and co-workers110 exploited the amidation reaction to chemically graft spiropyrans to CNTs, and used such a hybrid system to regulate horseradish peroxidase (HRP) activity via light irradiation (Fig. 5b). On ultraviolet light irradiation, the hybrid system showed enhanced catalytic HRP activity, which comes from the synergetic effect of CNTs and the merocyanine form of spiropyrans. The enhancement in the catalytic HRP activity has been used as a label-free colorimetric assay of lysozyme with a detection limit of 30nM. The high selectivity is due to the specific binding between lysozyme and aptamer. This approach does not need to covalently attach photochromic molecules on proteins and can be applicable to regulate the activity of other natural proteins using light. In another report, Lee et al.111 prepared a nanocomposite material assembled from azobenzene functionalized graphene oxide and stilbene-metal organic frameworks, which is capable of luminescent quenching by explosive gases. This unique system displays selectivity to dinitrotoluene (71% quenching) over trinitrotoluene (20% quenching) with sub-p.p.m. sensitivity and response times of less than a minute. This study opens a route towards the design molecularly well-defined materials possessing rapid, reversible and gas-selective fluorescent quenching capabilities. Yang et al.112 designed a nanocomposite consisting of a silyl-appended spiropyran and graphene oxide, which has been used as a chemosensor for the rapidly, selectively and sensitively colourimetric detection of fluoride ions in aqueous solution based on a specific chemical reaction. A nucleophilic reaction between silyl-appended spiropyran and fluoride ions promoted the ring-opening process, thus leading to increased absorption and colour change from colourless to orange-yellow. Graphene oxide could shorten the response time of silyl-appended spiropyran to 1/6 and lower the detection limit more than one order of magnitude, due to the large specific surface area and hydrophilic groups on graphene oxide improving the solubility of the silyl-appended spiropyran. The fast, selective and accurate determination of fluoride ions holds great potential in both environmental and biological systems. Using a similar strategy, they further extended the nanocomposite system in bioimaging of fluoride ions due to the nanocarrier function of graphene oxide for cells113. This approach will promote the further exploration of more effective fluorescent nanodosimeters for other analytes. However, novel photochromic carbon-based nanomaterials enabling multi-analyte detection via the observation of different signal outputs should be designed with the ultimate goal of discriminating analytes having similar structure/property, towards the fabrication of an artificial nose.
The ability to modulate structure and function in response to energy input and external signals is an important aspect also when implemented in biological systems, with the goal of realizing reversible switching of biological function between two different states (for example, inactive and active). Photochromic molecules have been used to modulate a number of important biological processes, such as protein folding, enzyme activity, membrane transport and so on. On the other hand, carbon-based nanomaterials are also widely employed for biomedical imaging, drug delivery and cancer therapy. Photochromic carbon-based nanomaterials capable of responding to a light input already showed to be active building blocks for biological applications, such as fluorescent probe for diagnosis and drug carrier in drug delivery system. For these purposes, photochromic carbon-based nanomaterials possessing a fast switching process and a large extinction coefficient with a high quantum yield is required. Del Canto et al. used amide coupling to link spiropyrans to CNTs, which showed light-modulated release of antinflammatory zinc ions52. The realization of potential photo-controllable spiropyran/CNTs based drug delivery systems is envisaged, where CNTs act as intracellular carriers of light-modulated receptors for bioactive agents. Park and co-workers114 demonstrated a strategy to prepare photo-responsive chemically rGO with mussel-inspired adhesive material dopamine and photochromic dye spiropyran conjugated to the backbone of the targeting ligand hyaluronic acid. rGO/hyaluronic acid-spiropyran could retain in vivo fluorescence imaging feature using confocal laser scanning microscope (Fig. 5c). Accumulation of rGO/hyaluronic acid-spiropyran in tumour tissue from biodistribution analysis strongly supports the specific delivery of prepared graphene to the target destination. Later on, the same group reported a stimuli-responsive fluorescent nanomaterial based on graphene oxide coupled with a polymer conjugated with photochromic spiropyran dye and hydrophobic boron dipyrromethane dye, for application in light-triggered target multicolour bioimaging115. The stability, biocompatibility and quenching efficacy of this nanocomposite open perspectives for cell imaging in different independent colours, sequentially and simultaneously. Although the above results are promising, the risk of using carbon-based materials in biological systems should be always considered, and designing photochromic molecules capable of switching with infrared light irradiation still need to be solved for the practical applications.
Photochromic carbon-based nanomaterials hold potential for applications in other emerging fields. For example, the use of azobenzenes blended with CNTs and polymers to form nanocomposites possessing light-induced conductance switching properties have been reported116,117. These nanocomposites appear as good candidates for electro-optical memories, smart windows or ‘smart labels' in packaging, in particular anti-counterfeit, applications.
Chemically rGO was functionalized with azobenzene-polymer brushes via surface initiated controlled radical polymerization, which was further used for photo-induced surface relief gratings67. Experimental results showed that light can be used to induce transport of graphene sheets within the molecular glass matrix on the micrometre scale. Mechanically cleavaged multilayer graphene was exploited as a nanoscopic probe to characterize local opto-mechanical forces generated within photosensitive polymer films containing azobenzene units118. On irradiation with light interference patterns, photosensitive films deform according to the spatial intensity variation, leading to the formation of periodic topographies such as surface relief gratings with internal pressure exceeding 1GPa. This study opens the possibility to characterize opto-mechanical forces generated within photo-responsive polymer films.
Unlike macroscopic motion in real-world systems, molecular systems are constantly undergoing Brownian motions. Because of this reason harnessing molecular motion unidirectionally is a far more difficult challenge. Nanovehicles are one kind of molecular machines having a chassis connected to wheel-terminated axles, which can convert energy inputs into motion on a surface in a controlled manner, by bridging the gap between synthetic molecular systems and the machines of the macroscopic world. From the synthetic point of view, synthesis of nanovehicles itself from ‘bottom-up' using molecular building blocks is quite demanding and challenging. Photochromic carbon-based nanomaterials based on fullerenes are used for the design of nanovehicles, by taking advantage of the remarkably different dipole moments and nanoscale mechanics of the photochromic isomers and the perfect spherical structure of fullerene. Tour and co-workers119 designed a branched azobenzene-fullerene-based nanostructure to realize a nanovehicle aiming to move like a caterpillar. Despite the designed nanovehicle did not show any movement on surfaces, this seminal work represents a source of inspiration for future design of nanovehicles containing photochromic carbon-based nanomaterials. Nowadays a major challenge remains the synthesis of new vehicles capable of travelling over long distances with an atomic precision in the motion at surfaces and an exquisite directional control.
Highly ordered fullerene arrays were constructed at the liquid/solid interface by co-adsorption of fullerenes and a supramolecular template using an azobenzene derivative120. Other systems combining large polycyclic aromatic hydrocarbons with photochromic molecules self-assembled at the liquid/solid interface were also reported121,122. These studies provide new insights on how to control dynamic self-assembly on surfaces. Self-assembled graphene/azo polyelectrolyte multilayer film held potential use in electrochemical energy storage devices123. Interestingly, three-dimensional polyphenylene dendrimers combined with azobenzenes were used as light-driven encapsulation of guest molecules into interior cavities, which is important for the design of new drug delivery systems124. As a follow-up of this work, Müllen and colleagues125 further designed azobenzene–polyphenylene dendrimers with a borate anions core, which showed a reversible change in the conductivity of electrolyte solutions of the salt on light irradiation. This is due to photo-induced changes in the overall size of the dendronized anion and the density of its polyphenylene shell. A molecular ‘hexad' consists of five bis(phenylethynyl)anthracene fluorophores, a dithienylethene photochrome and a central hexaphenylbenzene unit has been synthesized and used as a photochemical ‘triode' molecular signal transducer126. Remarkably, multiple modulations such as fluorescence, frequency, amplitude and phase can be realized. However, the synthesis of the three molecules is challenging124,125,126, which may hinder their practical applications. All of these studies have largely broadened the application scope of photochromic carbon-based nanomaterials.
The progress of photochromic carbon-based nanomaterials meets the growing requirement for environmental friendly and smart materials, largely depending on advanced material design and characterization techniques86. Reduced response time combined with enhanced light sensitivity and electronic modulation of photochromic carbon-based materials will be key for the development of novel multifunctional responsive materials, for example, smart windows, new type of photodetectors, ultra-light weight photonic and electronic devices, flexible sensors and so on. When combined with cheap processing method, such as inkjet printing, spray-coating or roll-to-roll, photochromic carbon-based nanomaterials can be expected to have a bright future towards low-cost, large-area and scale production. Photochromic carbon-based nanomaterials can be also applied further in biology by tethering them to biomolecules: the ability of sensing conformational changes can be used to detect modification of biological environments or biological based recognition events leading to conformation changes like protein folding.
Despite the rapid progress, the field of photochromic carbon-based nanomaterials is still not fully ripened. What are the bottlenecks in the development of photochromic carbon-based nanomaterials? Several challenges can be envisaged and should be addressed in the future development of this field. Further fundamental insights are required through a deeper investigation of the working principles for photochromic molecules tethered with carbon-based nanomaterials, in particular by unravelling the relationship between structures at the molecular/supramolecular level and the photo-responsive behaviour. Photophysical and photochemical processes of photochromic carbon-based nanomaterials are still far from being fully unveiled (for example, how are the charges spatially distributed on excitation and how is the photo-isomerization process affected by the interaction between photochromic molecules and carbon-based nanomaterials), being a colossal task that can be accomplished by combining spectroscopic investigations with modelling/simulation efforts. New and advanced characterization techniques are needed to bridge theories and experimental results. Optimization of the efficiency for light responsiveness and enhancement of the long-term photostability of the hybrid system should be also considered as important aspects for applications.
For solar thermal fuels to become feasible, photochromic carbon-based nanomaterials with a much greater packing density of active photochromic molecules are required such that the energy density can approach that of commercial batteries127. For example, the high surface strain of fullerenes may allow a much higher density of photochromic molecules to be attached. Besides azobenzene, other photochromic molecules like stilbene derivatives could be also considered for incorporation in carbon-based solar thermal fuels128. Another possibility to improve the performance of solar thermal fuels is to introduce bulky functional groups on the carbon-based templates, thus increasing the rigidity of the photochromic molecules. As for the application in molecular junctions, better control of the interfacial electronic coupling between carbon electrodes and photochromic molecules by rational design of the molecular backbone of the latter is needed. For instance, increasing the flexibility of the junction either by avoiding conjugated bonds instead using longer saturated carbon linkers/metaphenyl or by enlarging the electrode mobility. For memory devices, a high Ion/Ioff current ratio, long-term stability, excellent reversibility and reproducibility, further increasing the rates of data storage and storage densities (multilevel memory states), are required to meet the criteria of practical data storage technology. Combining large-area, high-quality graphene from chemical vapour deposition process with photochromic molecules, meanwhile improving the reproducibility and cycle stability, are the obstacles to be tackled for application in transistors. An important concern in photochromic carbon-based nanodevices is whether the observed phenomena are truly due to the effects of photochromes or just a result of extrinsic switching. Therefore, control experiments should be always performed. A more delicate design via incorporating enhanced components combining photochromic molecules (for example, synthetic molecular motors129) with carbon-based nanomaterials is needed to realize controlled motion on a surface. Developing advanced imaging technique including scanning probe microscopies, fluorescence microscopy and nanoscopies is indispensable to observe the motion of nanovehicles at different length scales, from the sub-nanometer to the hundreds of micrometres scale. For practical applications in sensing, increasing the sensitivity, response speed and selectivity is a prerequisite. Multi-analyte sensing is a largely unexplored application in which photochromic carbon-based nanomaterials can hold great potential. Other photochromic molecules such as phenoxyquinone130 (Fig. 6) or dithienylethene derivatives could be also applied together with carbon-based nanomaterials for sensing.
How soon do we expect to see these developments? Basic research on constructing photochromic carbon-based nanomaterials with ad hoc properties is just starting, and further detailed studies are needed. The number of photochromic carbon-based nanomaterials is still limited, compared with the large amount of photochromic molecular systems which have been synthesized and investigated. However, one should bear in mind that some photochromic molecules seem not ideal to be coupled with carbon-based nanomaterials: for example, photochromic molecules relying on cycloadditions may react with the double bonds of carbon-based nanomaterials therefore losing the switching function. Besides the most widely used photochromic molecules discussed above, other photochromic systems such as dihydroazulene, fulgides/fulgimides, chromenes, hemithioindigo, retinal, quinones and so on, are also promising candidates to be coupled with carbon-based nanomaterials for specific applications. For instance, retinal or hemithioindigo combined with carbon-based nanomaterials could be useful for biological applications. Currently, the possibility of switching the magnetic properties of functional (nano)materials is gathering an increased attention. Photo-generated radical compounds131 or photo-induced valence tautomeric metal complexes132 are normally accompanied by reversible and distinct changes in their physical properties especially in magnetic property (Fig. 6). Combing them with carbon-based nanomaterials holds the potential to reversibly tune the magnetic properties of both components, and can be key for applications in spintronics. A greater attention should be also paid to design hybrid systems that can be switched between more than two states using different stimuli. For the development of useful and practical photochromic carbon-based nanomaterials, we must further understand the mechanisms that induce these phenomena to establish a true design strategy of the systems. All these studies will promote the design of well-defined structures and their self-assembly behaviour for novel photochromic carbon-based nanomaterials, ultimately paving the way towards new generation of responsive multifunctional (nano)materials.
How to cite this article: Zhang, X. et al. Coupling carbon nanomaterials with photochromic molecules for the generation of optically responsive materials. Nat. Commun. 7:11118 doi: 10.1038/ncomms11118 (2016).
This work was supported by the European Commission through the Graphene Flagship (GA-604391), the FP7-NMP-2012-SMALL-6 ‘SACS' project (GA-310651), the ERC project SUPRAFUNCTION (GA-257305) and the Marie Curie ITN project iSwitch (GA No. 642196), as well as the Agence Nationale de la Recherche through the LabEx CSC (ANR-10-LABX-0026_CSC), the International Center for Frontier Research in Chemistry (icFRC).