Time-resolved Microwave Conductivity Research Articles

Electronic relaxation in PLD TiO2 films processed with femtosecond UV-laser

Modifications of shallow electron trap states near conduction band was analyzed after surface structuring of TiO2 thin films prepared via pulsed laser deposition method. Laser-induced periodic surface structures (LIPSS) were produced on the large-area films after irradiation with femtosecond KrF laser (λ = 248 nm). While spatial period of LIPSS Λ ≈ 190 ± 10 nm was not affected by laser fluence, coherence was increased with an increase of laser dose. Time-resolved microwave conductivity measurements accompanied by theoretical modelling revealed energetic positions of shallow electron trap states, connected to LIPSS. A possibility to alter the trap states energy via surface structuring of the material was shown.

Identification and Dynamics of Microsecond Long-Lived Charge Carriers for CsPbBr3 Perovskite Quantum Dots, Featuring Ambient Long-Term Stability.

We analyze the stability and photophysical dynamics of CsPbBr3 perovskite quantum dots (PeQDs), fabricated under mild synthetic conditions and embedded in an amorphous silica (SiOx) matrix (CsPbBr3@SiOx), underscoring their sustained performance in ambient conditions for over 300 days with minimal optical degradation. However, this stability comes at the cost of a reduced photoluminescence efficiency. Time-resolved spectroscopic analyses, including flash-photolysis time-resolved microwave conductivity and time-resolved photoluminescence, show that excitons in CsPbBr3@SiOx films decay within 2.5 ns, while charge carriers recombine over approximately 230 ns. This longevity of the charge carriers is due to photoinduced electron transfer to the SiOx matrix, enabling hole retention. The measured hole mobility in these PeQDs is 0.880 cm2 V-1 s-1, underscoring their potential in optoelectronic applications. This study highlights the role of the silica matrix in enhancing the durability of PeQDs in humid environments and modifying exciton dynamics and photoluminescence, providing valuable insights for developing robust optoelectronic materials.

Modification of Visible-Light-Responsive Pb2Ti2O5.4F1.2 with Metal Oxide Cocatalysts to Improve Photocatalytic O2 Evolution toward Z-Scheme Overall Water Splitting.

The development of a highly active photocatalyst for visible-light water splitting requires a high-quality semiconductor material and a cocatalyst, which promote both the migration of photogenerated charge carriers and surface redox reactions. In this work, a cocatalyst was loaded onto an oxyfluoride photocatalyst, Pb2Ti2O5.4F1.2, to improve the water oxidation activity. Among the metal oxides examined as cocatalysts, RuO2 was found to be the most suitable, and the O2 evolution activity depended on the preparation conditions for Ru/Pb2Ti2O5.4F1.2. The highest activity was obtained with RuCl3-impregnated Pb2Ti2O5.4F1.2 heated under a flow of H2 at 523 K. The H2-treated Ru/Pb2Ti2O5.4F1.2 showed an O2 evolution rate an order of magnitude higher than those for the analogues without the H2 treatment (e. g., RuO2/Pb2Ti2O5.4F1.2). Physicochemical analyses by X-ray absorption fine-structure spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and time-resolved microwave conductivity measurements indicated that the optimized photocatalyst contained partially reduced RuO2 species with a particle size of ~5 nm. These partially reduced species effectively trapped the photogenerated charge carriers and promoted the oxidation of water into O2. The optimized Ru/Pb2Ti2O5.4F1.2 could function as an O2-evolving photocatalyst in Z-scheme overall water splitting, in combination with an Ru-loaded, Rh-doped SrTiO3 photocatalyst.

Vacuum-Processed Propylene Urea Additive: A Novel Approach for Controlling the Growth of CH3NH3PbI3 Crystals in All Vacuum-Processed Perovskite Solar Cells.

In this study, we present a novel method for controlling the growth of perovskite crystals in the vacuum thermal evaporation process by utilizing a vacuum-processable additive, propylene urea (PU). By coevaporation of perovskite precursors with PU to form the perovskite layer, PU, acting as a Lewis base additive, retards the direct reaction between the perovskite precursors. This facilitates a larger domain size and reduced defect density. Following the removal of the residual additive, the perovskite layer, exhibiting improved crystallinity, demonstrates reduced charge recombination, as confirmed by a time-resolved microwave conductivity analysis. Consequently, there is a notable enhancement in open-circuit voltage and power conversion efficiency, increasing from 1.05 to 1.15 V and from 17.17 to 18.31%, respectively. The incorporation of a vacuum-processable and removable Lewis base additive into the fabrication of vacuum-processed perovskite solar cells offers new avenues for optimizing these devices.

Tail states suppression via surface-modification of wide-bandgap perovskites for high-efficiency all-perovskite photovoltaic tandems

As an essential light-absorbing material in perovskite-based tandem solar cells, wide-bandgap (WBG) perovskite has garnered extensive attention. Nevertheless, due to severe non-radiative recombination from tail states, as well as photoinduced phase segregation and unoptimized charge transfer, WBG perovskite solar cells (PSCs) typically display significant open-circuit voltage (VOC) loss and low fill factor (FF). In this work, we report to modify the 1.68 eV WBG perovskite film upon optimized surface passivation with 1,3-propane-diammonium iodide (PDAI2). Time-resolved microwave conductivity measurement is employed to analyze the tail states, mobilities of charge carriers and the rate constants of recombination in perovskite films. The results indicate that the optimized surface modification strategy not only enhances film quality, boosts carrier transport, but also suppresses tail states and therefore diminishes non-radiative recombination, consequently elevating the VOC and FF of the device. Hence, the PDAI2-assisted WBG PSCs deliver an optimal efficiency of 21.48 %, accompanied by a VOC of 1.243 V. Furthermore, the integration of a narrow-bandgap tin–lead PSC with a semi-transparent WBG PSC results in a four-terminal perovskite/perovskite tandem solar cell, showcasing an efficiency surpassing 28 %. Our research offers a practical approach for producing efficient WBG PSCs and tandem solar cells.

Missing Excitons: How Energy Transfer Competes with Free Charge Generation in Dilute-Donor/Acceptor Systems.

Energy transfer across the donor-acceptor interface in organic photovoltaics is usually beneficial to device performance, as it assists energy transport to the site of free charge generation. Here, we present a case where the opposite is true: dilute donor molecules in an acceptor host matrix exhibit ultrafast excitation energy transfer (EET) to the host, which suppresses the free charge yield. We observe an optimal photochemical driving force for free charge generation, as detected via time-resolved microwave conductivity (TRMC), but with a low yield when the sensitizer is excited. Meanwhile, transient absorption shows that transferred excitons efficiently produce charge-transfer states. This behavior is well described by a competition for the excited state between long-range electron transfer that produces free charge and EET that ultimately produces only localized charge-transfer states. It cannot be explained if the most localized CT states are the intermediate between excitons and the free charge in this system.

Non-resonant phase sensitive approach for time resolved microwave conductivity in photoactive thin films

Time-resolved microwave conductivity (TRMC) is a contactless technique utilized for the investigation of carrier density, transport properties, trapping phenomena, and recombination parameters in charge transport materials. Traditional TRMC methods rely on resonant cavities or resonators, which impose limitations on the frequency range and accuracy of measurements. In this study, we introduce an innovative approach that employs a non-resonant coplanar transmission line and a microwave interferometric detection scheme to investigate the phase-dependent complex microwave conductivity. Additionally, we demonstrate unique calibration techniques for determining the absolute complex microwave conductivity by combining transient photoconductivity (TPC) and electron spin resonance (ESR) as complementary methods. By utilizing a phase-sensitive microwave interferometer, our detection scheme significantly enhances measurement sensitivity and eliminates the need for a resonant cavity. This broadband detection system enables direct measurement of phase-dependent changes in film conductivity (Δσ). Moreover, it allows us to measure subtle variations in sample photoconductivity upon optical excitation and accommodates greatly restricted volumes (∼nL) consistent with typical device sizes. Here we demonstrate the utility of this technique on a series of poly(3-hexylthiophene) (P3HT) and the electron acceptor [6,6]-phenylC61-butyric acid methyl ester (PCBM) thin films with varying concentrations of PCBM and film thickness.

Exploration of Solution-Processed Bi/Sb Solar Cells by Automated Robotic Experiments Equipped with Microwave Conductivity.

Solution-processed inorganic solar cells with less toxic and earth-abundant elements are emerging as viable alternatives to high-performance lead-halide perovskite solar cells. However, the wide range of elements and process parameters impede the rapid exploration of vast chemical spaces. Here, we developed an automated robot-embedded measurement system that performs photoabsorption spectroscopy, optical microscopy, and white-light flash time-resolved microwave conductivity (TRMC). We tested 576 films of quaternary element-blended wide-bandgap Cs-Bi-Sb-I semiconductors with various compositions, organic salt additives (MACl, FACl, MAI, and FAI, where MA and FA represent methylammonium and formamidinium, respectively), and thermal annealing temperatures. Among them, we found that the maximum power conversion efficiency (PCE) was 2.36%, which is significantly higher than the PCE of 0.68% for a reference film without an additive. Machine learning (ML) and statistical analyses revealed significant features and their relationships with TRMC transients, thereby demonstrating the advantages of combining ML and automated experiments for the high-throughput exploration of photovoltaic materials.

(Keynote) Recent Insights on Carrier Generation, Transport, and Extraction in Metal Oxide Photoelectrodes

After the absorption of light, the next steps in any artificial photosynthetic system are the generation, transport, and extraction of photoexcited charge carriers. These steps are well understood in solid state systems based on traditional semiconductors, such as Si and III-V absorbers, resulting in quantum efficiencies close to one for optimized devices. For metal oxide-based absorbers, which have attracted much interest in the past decades because of their relatively good (photo)chemical stability and low cost, the reported efficiencies tend to be much lower. This is often attributed to recombination at defects. While these may indeed adversely affect the efficiency, there are several other fundamental loss mechanisms in metal oxides that are not always fully appreciated. For example, certain metal ions exhibit localized d-d transitions that do not result in mobile charge carriers, resulting in a photogeneration yield < 1. Recent work showed that it is possible to quantify the fraction of mobile photoexcited carriers, from which an upper limit of the achievable photocurrent can be derived [1]. Losses can also occur in the form of recombination or carrier localization during transport. The chance of reaching the interface is often expressed as the carrier diffusion length, which in turn depends on the carrier lifetime and its mobility. Convenient contact-free methods to determine these parameters are time-resolved microwave conductivity (TRMC) and time-resolved THz spectroscopy (TRTS) [2]. Here, one of the challenges is to determine whether the decay in photoconductivity is due to a decay in carrier concentration (i.e., recombination), carrier mobility (trapping, polaron formation), or both. We recently developed a general analysis method for determining the diffusion length which is valid for time-dependent mobilities as well as time-dependent lifetimes [3]. Intringuingly, this method revealed a carrier diffusion length of only 15 nm for BiVO4, which is significantly shorter than previously reported values by us and others. The only way this short diffusion length can be reconciled with the high photocurrent densities reported for this material is by assuming field-assisted charge separation. The role of the electric field is, however, poorly understood in the photoelectrochemistry and photocatalysis communities [4]. In a system without externally applied bias, the electric field does not separate the charges; instead, charge separation is driven by the presence of selective contacts. During my presentation I will review these concepts and discuss how a better understanding of loss mechanisms, the role of the electric field, and selective contacts may help us design more efficient metal oxide-based photoelectrodes.

Perovskite Solar Cell Using Isonicotinic Acid as a Gap-Filling Self-Assembled Monolayer with High Photovoltaic Performance and Light Stability.

High photovoltaic performance and light stability are required for the practical outdoor use of lead-halide perovskite solar cells. To improve the light stability of perovskite solar cells, it is effective to introduce a self-assembled monolayer (SAM) between the carrier transport layer and the perovskite layer. Several alternative approaches in their molecular design and combination with multiple SAMs support high photovoltaic conversion efficiency (PCE). Herein, we report a new structure for improving both PCE and light stability, in which the surface of an electron transport layer (ETL) was modified by combining a fullerene-functionalized self-assembled monolayer (C60SAM) and a suitable gap-filling self-assembled monolayer (GFSAM). Small-sized GFSAMs can enter the gap space of the C60SAM and terminate the unterminated sites on the ETL surface. The best GFSAM in this study was formed using an isonicotinic acid solution. After a light stability test for 68 h at 50 °C under 1 sun illumination, the best cell with C60SAM and GFSAM showed a PCE of 18.68% with a retention rate of over 99%. Moreover, following outdoor exposure for six months, the cells with C60SAM and GFSAM exhibited almost unchanged PCE. From the valence band spectra of the ETLs obtained using hard X-ray photoelectron spectroscopy, we confirmed a decrease in the offset at the ETL/perovskite interface owing to the additional GFSAM treatment on the C60SAM-modified ETL surface. Time-resolved microwave conductivity measurements demonstrated that the additional GFSAM improved electron extraction at the C60SAM-modified ETL/perovskite interface.

Charge Concentration Limits the Hydrogen Evolution Rate in Organic Nanoparticle Photocatalysts.

Time-resolved microwave conductivity is used to compare aqueous-soluble organic nanoparticle photocatalysts and bulk thin films composed of the same mixture of semiconducting polymer and non-fullerene acceptor molecule and the relationship between composition, interfacial surface area, charge-carrier dynamics, and photocatalytic activity is examined. The rate of hydrogen evolution reaction by nanoparticles composed of various donor:acceptor blend ratio compositions is quantitatively measured, and it is found that the most active blend ratio displays a hydrogen quantum yield of 0.83% per photon. Moreover, it is found that nanoparticle photocatalytic activity corresponds directly to charge generation, and that nanoparticles have 3× more long-lived accumulated charges relative to bulk samples of the same material composition. These results suggest that, under the current reaction conditions, with ≈3× solar flux, catalytic activity by the nanoparticles is limited by the concentration of electrons and holes in operando and not a finite number of active surface sites or the catalytic rate at the interface. This provides a clear design goal for the next generation of efficient photocatalytic nanoparticles.

Charge-Carrier Dynamics of Evaporated Bismuth-Based Chalcogenide Thin Films Probed with Time-Resolved Microwave Conductivity.

Chalcogenide-based semiconductors are emerging as a set of highly promising candidates for optoelectronic devices, owing to their low toxicity, cost-effectiveness, exceptional stability, and tunable optoelectronic properties. Nonetheless, the limited understanding of charge recombination mechanisms and trap states of these materials is impeding their further development. To fill this gap, we conducted a comprehensive study of bismuth-based chalcogenide thin films and systematically investigated the influence of post-treatments via time-resolved microwave conductivity and temperature-dependent photoluminescence. The key finding in this work is that post-treatment with Bi could effectively enhance the crystallinity and charge-carrier mobility. However, the carrier density also increased significantly after the Bi treatment. On the contrary, post-treatment of evaporated Bi2S3 thin films with sulfur could effectively increase the carrier lifetime and mobility by passivating the trap states on the grain boundaries, which is also consistent with the enhanced radiative recombination efficiency.

Solution-processed bismuth sulfide incorporated with zinc for high-gain and low-noise photodetection

Bismuth sulfide possesses an extremely high absorption coefficient, a relatively small bandgap, and high charge carrier mobility, which are favorable for photovoltaics and photodetection. However, the device performance of binary Bi2S3 is still limited by the poor charge transport and complicated trap features caused by the stoichiometric imbalance, as both sulfur vacancy and bismuth vacancy could result in tremendous trap states. In this work, we incorporate a small amount of extrinsic elements in the solution-processed Bi2S3 thin films and systematically investigate the influence of extrinsic doping on the charge transport properties of Bi2S3 thin films via time-resolved microwave conductivity and field-effect transistors. We also fabricate photodetectors based on these Zn2+ incorporated Bi2S3 thin films and achieve state-of-the-art device performance, including relatively high on/off ratio, high responsivity, and extremely low dark current and noise, which is promising for next-generation solution-processed photodetection.

Suppressing Phase Segregation in CsPbIBr2 Films via Anchoring Halide Ions toward Underwater Solar Cells

Inorganic CsPbIBr2 perovskite solar cells (PSCs) have accomplished many milestones, yet their progress has been constrained by ion migration and phase separation. This study explores the modulation of perovskite crystallization kinetics and halide ion migration through chlorobenzene (CB) antisolvent with bis(pentafluorophenyl)zinc (Zn(C6F5)2) additive. The photoluminescence and absorption spectra reveal the significantly reduced phase segregaton in CsPbIBr2 film treated by CB with Zn(C6F5)2. Moreover, this research analyzes the CsPbIBr2 film's free carrier lifetime, diffusion length, and mobility using time-resolved microwave conductivity and transient absorption spectroscopy after Zn(C6F5)2 modification. Consequently, the modified CsPbIBr2 PSCs offer a 12.57% power conversion efficiency (PCE), the highest value among CsPbIBr2 PSCs with negligible hysteresis and prolonged stability. Furthermore, under 1-m-deep water, CsPbIBr2 PSCs display a PCE of 14.18%. These findings provide an understanding of the development of phase-segregation-free CsPbIBr2 films and showcase the prospective applications of CsPbIBr2 PSCs in underwater power systems.

Comprehensive evaluation of copper vanadate (α-CuV2O6) for use as a photoanode material for photoelectrochemical water splitting

This study is an initial account of solution-based spray pyrolysis-produced n-type copper vanadate (CuV2O6) thin film photoanodes. CuV2O6 photoelectrodes have been tested for their ability to oxidize water in aqueous (pH 6.8) solutions using photoelectrochemical (PEC) tests. The band edge positions, band gap energy, photocurrent generation, flat band potential, chemical make-up, chemical stability, charge carrier transit, and O2 production faradic efficiency are a few of the physical and photophysical features measured and described. According to the findings, CuV2O6 possesses a satisfactory bandgap of 1.9 eV and appropriate band locations that allow for the use of visible light for overall solar water splitting. Under AM1.5 simulated sunlight, the maximum photocurrent density recorded is 0.18 mA cm− 2 at 1.23 VRHE with Na2SO3 acting as a hole scavenger. As evidenced by film shape, surface compositions before and after the PEC measurements, and outstanding structural and compositional stability throughout the oxygen evolution reaction (OER), the CuV2O6 photoelectrodes performed well. CuV2O6 photoanodes also exhibit almost a unit faradic efficiency for the oxidation of water. The overall photoelectrochemical efficiency, however, is constrained by the photogenerated charge carriers' weak mobility (∼8 ×10−3 cm2 V−1 s−1), short lifetime (∼20 ns), and limited hole diffusion length (∼20.4 nm), according to time-resolved microwave conductivity (TRMC) tests. Based on the current findings, this study offers new insight into building enhanced high-quality CuV2O6 photoanodes by methodically clarifying numerous important physical and photoelectrochemical characteristics for the photooxidation of water.

Trapped Carrier Recombination in Sb2Se3 Polycrystalline Film

Sb2Se3 has recently emerged as a promising material for optic-electronic applications. In this work, trapped carrier recombination in Sb2Se3 was investigated by joint use of time-resolved microwave conductivity (TRMC) and photoluminescence (PL) spectroscopy. trapped carrier thermal excitation into the continuous band was observed in TRMC kinetics. Based on the exponential band tail model, the depth of the trap state, where trapped carriers are released into a continuous band, was estimated to range from 33.0 meV to 110.0 meV at room temperature. Temperature-varying TRMC and PL were further employed to study the influence of temperature on the trapped carrier recombination. Negative thermal quenchings of PL intensity and quantity of thermal emission carriers were observed and can be well explained by the thermal excitation of deep trapped carriers into shallow trap states and the continuous band. Two thermal activation energies of 12.5 meV and 304.0 meV were also revealed. This work is helpful for understanding the trapped carrier recombination process in polycrystalline Sb2Se3 film.

Resolving Complex Photoconductivity of Perovskite and Organic Semiconductor Films Using Phase-Sensitive Microwave Interferometry

Complex transient photoconductivity (Δσ) contains rich fingerprints of charge recombination dynamics in photoactive films. However, a direct measure of both real (Δσ′) and imaginary (Δσ″) components has proven difficult using conventional cavity-based time-resolved microwave conductivity approaches. Here, we present a novel approach to resolve Δσ′ and Δσ″ parts of Δσ by using a nonresonant coplanar transmission line and a microwave interferometric detection scheme. The use of a phase-sensitive microwave interferometer greatly increases the measurement sensitivity and eliminates the requirement of a resonant cavity. This broadband detection scheme allows for direct measurement of Δσ. The relationship between the experimental phase shift and Δσ′ and Δσ″ components is decoded through an in situ electron spin resonance (ESR) measurement. ESR line shape analysis is used to confirm the assignment of the transients to the Δσ′ and Δσ″ components. We demonstrate the utility of this technique on thin films of poly(3-hexylthiophene): [6,6]-phenylC61-butyric acid methyl ester (P3HT:PCBM) and perovskite MA0.85FA0.15PbI3 films on glass.

Elucidation of a Photothermal Energy Conversion Mechanism in Hydrogenated Molybdenum Suboxide: Interplay of Trapped Charges and Their Dielectric Interactions

Hydrogenated molybdenum suboxide (HxMoO3-y) is a promising photothermal energy conversion (PEC) material. However, its charge carrier dynamics and underlying mechanisms remain unclear. Utilizing flash-photolysis time-resolved microwave conductivity, we investigated charge carrier-dielectric interactions in the Pt/HxMoO3-y composite. The charge recombination of H2-reduced Pt/HxMoO3-y was 2-3 orders of magnitude faster than that of Pt/MoO3, indicating efficient PEC. A complex photoconductivity study revealed that Pt/HxMoO3-y has two types of trapping mechanisms, Drude-Zener (DZ) and negative permittivity effect (NPE) modes, depending on the reduction temperature. Pt/HxMoO3-y reduced at 100 °C exhibited a dominant NPE owing to the electrical interaction of trapped charges with the surrounding ions and/or OH base. This polaronic trapped state retarded the PEC process. We found Pt/HxMoO3-y reduced at 200 °C to be optimal owing to the balanced suppression of the NPE and charge diffusion. This is the first report revealing the charge dynamics in hydrogenated metal oxides and their impacts on PEC processes.

Shallow traps-induced ultra-long lifetime of metal halide perovskites probed with light-biased time-resolved microwave conductivity

Metal halide perovskites have emerged as promising candidates for next-generation optoelectronics. However, the present understanding of their recombination processes and trap states within the devices are still limited, which is also inevitable in the state-of-the-art perovskite solar cells with multiple passivation strategies and various additives involved. Recent works have also demonstrated that metal cations incorporated perovskites could potentially reduce the non-radiative losses and improve the device performance to some extent. However, the underlying “doping” mechanism is not clear. In this work, we systematically investigated the trap-induced ultra-long carrier lifetime of the metal cation incorporated perovskites and found that some specific cations could extend the carrier lifetime up to ∼100 μs, which could be correlated with the formation of shallow trap states. In addition, such shallow trap-mediated charge dynamics could be effectively probed with light-biased time-resolved microwave conductivity technique, which provides additional information to conventional time-resolved photoluminescence.

Supramolecular Recognition within a Nanosized "Buckytrap" That Exhibits Substantial Photoconductivity.

We report here a nanosized "buckytrap", 1, constructed from two bis-zinc(II) expanded-TTF (exTTF) porphyrin subunits. Two forms, 1a and 1b, differing in the axial ligands, H2O vs tetrahydrofuran (THF), were isolated and characterized. Discrete host-guest inclusion complexes are formed upon treatment with fullerenes as inferred from a single-crystal X-ray structural analyses of 1a with C70. The fullerene is found to be encapsulated within the inner pseudohexagonal cavity of 1a. In contrast, the corresponding free-base derivative (2) was found to form infinite ball-and-socket type supramolecular organic frameworks (3D-SOFs) with fullerenes, (2•C60)n or (2•C70)n. This difference is ascribed to the fact that in 1a and 1b the axial positions are blocked by a H2O or THF ligand. Emission spectroscopic studies supported a 1:1 host-guest binding stoichiometry, allowing association constants of (2.0 ± 0.5) × 104 M-1 and (4.3 ± 0.9) × 104 M-1 to be calculated for C60 and C70, respectively. Flash-photolysis time-resolved microwave conductivity (FP-TRMC) studies of solid films of the Zn-complex 1a revealed that the intrinsic charge carrier transport, i.e., pseudo-photoconductivity (ϕ∑μ), increases upon fullerene inclusion (e.g., ϕ∑μ = 1.53 × 10-4 cm2 V-1 s-1 for C60⊂(1a)2 and ϕ∑μ = 1.45 × 10-4 cm2 V-1 s-1 for C70⊂(1a)2 vs ϕ∑μ = 2.49 × 10-5 cm2 V-1 s-1 for 1a) at 298 K. These findings provide support for the notion that controlling the nature of self-assembly supramolecular constructs formed from exTTF-porphyrin dimers through metalation or choice of fullerene can be used to regulate key functional features, including photoconductivity.