Light-induced Conductivity Research Articles

One-Pot Fabrication of Copper-Doped WO3·H2O Opto-Functional Layered Device using Submerged Photosynthesis of Crystallites.

This study introduces a one-pot, submerged photosynthesis of crystallites (SPsC) method for fabricating monohydrate tungstic acid (WO3·H2O) nanoplates directly integrated onto a stainless steel mesh, offering a simplified production and enhanced device stability for optical functional applications. The fabricated devices demonstrate exceptional broadband light absorption across the ultraviolet (UV), visible (Vis), and near-infrared (NIR) ranges. Notably, 1% Cu doping significantly boosts the NIR absorption, yielding a high solar utilization efficiency of 81.40%. In solar water evaporation experiments, the devices exhibit a maximum temperature increase of 13 °C under 1-Sun (100 mW/cm2) illumination, achieving an energy conversion efficiency of 32.5%. Moreover, electrochemical characterization reveals light-induced conductivity changes and enhanced current density, suggesting potential applications in rectifying devices. This versatile and environmentally conscious SPsC fabrication method holds promise for the sustainable development of diverse nanodevices.

Light-Induced Conductance Potentiation and Depression in an All-Optically Controlled Memristor.

Optoelectronic memristors are new multifunctional devices with both electrically tunable and light-tunable synaptic plasticity, attracting great attention as key promising devices for optoelectronic neuromorphic computing systems. At present, the conductance modulation in most optoelectronic memristors is conducted in a hybrid photoelectric mode, suffering some problems such as heat generation and control complexity. Here, an optoelectronic memristor based on the p+-Si/n-ZnO heterojunction is proposed where the conductance can be reversibly modulated in an all-optically controlled mode. The electron detrapping/trapping mechanism at the p+-Si/n-ZnO interface barrier region is presented to explain the light-induced conductance potentiation/depression behavior. Furthermore, some synaptic functions, including excitatory postsynaptic current (EPSC), inhibitory postsynaptic current (IPSC), and paired-pulse facilitation (PPF), are successfully mimicked in the p+-Si/n-ZnO heterojunction memristor, instructing its application potential for optoelectronic neuromorphic computing.

Reconfigurable intelligent surface and switchable electromagnetic interference shield based on dynamically adjustable composite film of cellulose nanofibers and VO2 nanoparticles

The emerging fields of 5G and 6G telecommunication networks, Internet of Things, and artificial intelligence have intensified the demand for green nanostructured materials with adjustable and intelligent features that respond to external stimuli. By leveraging the insulator-to-metal transition of VO2 nanoparticles, responsive composite films were developed by integrating these nanoparticles within a biopolymeric network of cationic cellulose nanofibers (CNF+). These films exhibit a reversible change in GHz permittivity upon exposure to thermal or optical stimuli, facilitating dynamic control of their electrical properties. The layered structure of the films further enhances their robustness, featuring a VO2 nanoparticle core encased within CNF+ layers. This design not only strengthens the structure but also significantly boosts light-induced conductivity, particularly in layered variant, underscoring its potential in optoelectronic applications. Simulation studies reveal that the nonuniform, reconfigurable intelligent surface (RIS) of the developed mixed film adeptly manipulates incident electromagnetic waves, making it suitable for 5G/6G wireless signals. Conversely, the layered film serves as a switchable electromagnetic interference (EMI) shield, demonstrating notable differences in shielding efficiency between its hot and cold states. Consequently, CNF+/VO2 composite films designed in this work emerge as a versatile, adaptable platform for intelligent electronics, particularly in the realm of 5G/6G wireless communications.

Correlation in Structural Architecture toward Fabrication of Schottky Device with a Series of Pyrazine Appended Coordination Polymers.

Energy is the center of importance for the survivability of civilization. Use of fossil fuel is going to be suspended, and renewable energy is technologically costlier. In the quest for new energy sources and to minimize fuel expenditure, the design of energy efficient devices is one of the solutions. Toward this objective, highly delocalized π-acidic N-hetreocycle pyrazine bridged Cd(II)-based coordination polymers (CPs), [Cd(tppz)(adc)(MeOH)] (1), [Cd(tppz)(trep)] (2), and [Cd(tppz)(2,6-ndc)] (3; tppz = 2,3,5,6-tetrakis(2-pyridyl)pyrazine) are synthesized in combination with π-accessible dicarboxylato linkers (acetylene dicarboxylic acid (H2adc), terephthalic acid (H2trep), and 2,6-naphthalene dicarboxylic acid (2,6 H2ndc)). The structures of the compounds, 1-3, have been confirmed by single-crystal X-ray diffraction measurements. Analysis of electrical property demonstrates that light irradiation enhances the conductivity and follows the order 3 > 2 > 1; compound 3 possesses the highest conductivity (1.93 × 10-3 (light), 1.12 × 10-4 S m-1 dark)), than 2 (1.80 × 10-4 (light), 1.10 × 10-4 S m-1 (dark)) and 1 (5.06 × 10-5 (light), 4.72 × 10-5 S m-1 (dark)). This light-induced electrical conductivity can pave the way toward fabrication of an active electronic device by using the discussed materials.

Guard Cell-Inspired Ion Channels: Harnessing the Photomechanical Effect via Supramolecular Assembly of Cross-Linked Azobenzene/Polymers.

Stimuli-responsive ion nanochannels have attracted considerable attention in various fields because of their remote controllability of ionic transportation. For photoresponsive ion nanochannels, however, achieving precise regulation of ion conductivity is still challenging, primarily due to the difficulty of programmable structural changes in confined environments. Moreover, the relationship between noncontact photo-stimulation in nanoscale and light-induced ion conductivity has not been well understood. In this work, a versatile design for fabricating guard cell-inspired photoswitchable ion channels is presented by infiltrating azobenzene-cross-linked polymer (AAZO-PDAC) into nanoporous anodic aluminum oxide (AAO) membranes. The azobenzene-cross-linked polymer is formed by azobenzene chromophore (AAZO)-cross-linked poly(diallyldimethylammonium chloride) (PDAC) with electrostatic interactions. Under UV irradiation, the trans-AAZO isomerizes to the cis-AAZO, causing the volume compression of the polymer network, whereas, in darkness, the cis-AAZO reverts to the trans-AAZO, leading to the recovery of the structure. Consequently, the resultant nanopore sizes can be manipulated by the photomechanical effect of the AAZO-PDAC polymers. By adding ionic liquids, the ion conductivity of the light-driven ion nanochannels can be controlled with good repeatability and fast responses (within seconds) in multiple cycles. The ion channels have promising potential in the applications of biomimetic materials, sensors, and biomedical sciences.

Disentangling the Competing Mechanisms of Light-Induced Anomalous Hall Conductivity in Three-Dimensional Dirac Semimetal.

We experimentally elucidate the origin of the anomalous Hall conductivity in a three-dimensional Dirac semimetal, Cd_{3}As_{2}, driven by circularly polarized light. Using time-resolved terahertz Faraday rotation spectroscopy, we determine the transient Hall conductivity spectrum with special attention to its sign. Our results clearly show the dominance of direct photocurrent generation assisted by the terahertz electric field. The contribution from the Floquet-Weyl nodes is found to be minor when the driving light is in resonance with interband transitions. We develop a generally applicable classification of microscopic mechanisms of light-induced anomalous Hall conductivity.

Photo-enhanced ionic conductivity across grain boundaries in polycrystalline ceramics.

Grain boundary conductivity limitations are ubiquitous in material science. We show that illumination with above-bandgap light can decrease the grain boundary resistance in solid ionic conductors. Specifically, we demonstrate the increase of the grain boundary conductance of a 3 mol% Gd-doped ceria thin film by a factor of approximately 3.5 at 250 °C and the reduction of its activation energy from 1.12 to 0.68 eV under illumination, while light-induced heating and electronic conductivity could be excluded as potential sources for the observed opto-ionic effect. The presented model predicts that photo-generated electrons decrease the potential barrier heights associated with space charge zones depleted in charge carriers between adjacent grains. The discovered opto-ionic effect could pave the way for the development of new electrochemical storage and conversion technologies operating at lower temperatures and/or higher efficiencies and could be further used for fast and contactless control or diagnosis of ionic conduction in polycrystalline solids.

Switching effects in plasmon circuits based on thin metal films and nanostructures with increased photoconductivity

The features of optical control of surface plasmon-polariton propagation in plasmon circuits based on thin metal waveguides and semiconductor nanostructures are considered. A model of a plasmon resonator with additional elements based on semiconducting materials exhibiting strong photoconductivity is proposed. By means of numerical simulation, the possibility of switching the surface plasmon-polariton flux in the plasmon circuit by switching on/off the external optical pumping field, which changes the contribution of light-induced conduction of control elements, is shown. Keywords: surface plasmon-polaritons, metal plasmon waveguide, photoconductivity, plasmon resonator.

Photosensitivity of semiconducting SeTeSb glasses

Photo-electrical measurements are done on thin films of SeTeSb to see the influence of Sb additive on the light-induced conduction of binary Se80Te20 alloy. The ratio of electrical conductivity under dark to light conditions has been measured for measuring the photosensitivity of the samples. The activation energies of conduction for dark and light conditions (∆Eph) are also determined. The results reveal that both σph / σd and ∆Eph are reduced with an increase in Sb concentration. This indicates that density of defect states (DDS) is increased with an increase in the concentration of foreign element (i.e., Antimony) in thin films of these glassy systems. The cause of the increase in defects is also discussed. Start your abstract here…

Solution-processed oxide semiconductor-based artificial optoelectronic synapse array for spatiotemporal synaptic integration

Optoelectronic neuromorphic systems mimicking the structure and the signal processing of biological neural systems have gained significant interest due to their potential advantages such as high computing speed, high bandwidth, parallel processing, and low power requirements. Here, we demonstrate an optoelectronic synapse array consisting of solution-processed indium-gallium-zinc-oxide (IGZO) synapse devices emulating complex neural functions such as the spatiotemporal synaptic integration for neuromorphic implementation. Particularly, we adopted a vertically stacked metal-insulator-semiconductor-metal structure for IGZO synapse device to enable efficient light-induced conductance update and a low-voltage operation typically below 3 V. Using light as the stimulation, versatile synaptic functions including short-term memory/long-term memory, symmetric spike-timing dependent plasticity, and spike-number dependent plasticity were mimicked. In addition, we obtained a high recognition accuracy of handwritten digit images up to 89.4% by implementing ADAM training algorithm. Furthermore, using a crossbar structure 3 × 3 IGZO synapse array, the emulation of spatiotemporal summation was successfully carried out which is believed to be responsible for the neural encoding and the auditory recognition processes occur in the brain.

Light-Dependent Impedance Spectra and Transient Photoconductivity in a Ruddlesden–Popper 2D Lead–Halide Perovskite Revealed by Electrical Scanned Probe Microscopy and Accompanying Theory

Electric force microscopy was used to record the light-dependent impedance spectrum and the probe transient photoconductivity of a film of butylammonium lead iodide, BA2PbI4, a 2D Ruddlesden–Popper perovskite semiconductor. The impedance spectrum of BA2PbI4 showed modest changes as the illumination intensity was varied up to 1400 mW cm–2, in contrast with the comparatively dramatic changes seen for 3D lead–halide perovskites under similar conditions. BA2PbI4’s light-induced conductivity had a rise time and decay time of ∼100 μs, 104 slower than expected from direct electron–hole recombination yet 105 faster than the conductivity-recovery times recently observed in 3D lead–halide perovskites and attributed to the relaxation of photogenerated vacancies. What sample properties are probed by electric force microscope measurements remains an open question. A Lagrangian-mechanics treatment of the electric force microscope experiment was recently introduced by Dwyer, Harrell, and Marohn which enabled the calculation of steady-state electric force microscope signals in terms of a complex sample impedance. Here this impedance treatment of the tip–sample interaction is extended, through the introduction of a time-dependent transfer function, to include time-resolved electrical scanned probe measurements. It is shown that the signal in a phase-kick electric force microscope experiment, and therefore also the signal in a time-resolved electrostatic force microscope experiment, can be written explicitly in terms of the sample’s time-dependent resistance (i.e., conductivity).

Light-induced high-spin state in ZnO nanoparticles

The effects of white-light irradiation on ∼15 nm diameter ZnO nanoparticles are investigated by means of electron paramagnetic resonance, near liquid-nitrogen and liquid-helium temperatures. Under dark conditions, usual core- and surface-defects are detected, respectively, at g = 1.960 and g = 2.003. Under white-light illumination, the core-defect signal intensity is strongly increased, which is to be correlated to the light-induced conductivity’s augmentation. Beside, a four-lines structure appears, with the same gravity center as that of the surface defects. Simulations and intensity power-dependence measurements show that this four-line-structure is very likely to arise from a localized high spin S = 2, induced by light irradiation, and subjected to a weak axial anisotropy. At 85 K, this high-spin state can last several hours after the light-irradiation removal, probably due to highly spin-forbidden recombination process. The possible excited resonant complexes at the origin of this signal are discussed. Other light-induced S = 1/2-like centers are detected as well, which depend on the nanoparticles growth conditions.

Light-induced non-Arrhenian conductivity of the single crystal methylammonium lead bromide perovskites

In the present communication, the conductivity of the single crystal methylammonium lead bromide as a function of temperature is studied. As a result, the activation energies for the dark/light conditions were determined. Interestingly, when the light illumination is applied, depending of the applied bias voltage, the complex conductivity response on the temperature changes was observed. Depending on the electrical field applied, the material follows two behaviors: first is typical of semiconductors and the second one and non-Arrhenian behavior, which is distinctive for metals. This is, for the best of our knowledge, the first observation of this unique property of single crystal methylammonium lead bromide perovskite.

Ion Channel Properties of a Cation Channelrhodopsin, Gt_CCR4

We previously reported a cation channelrhodopsin, Gt_CCR4, which is one of the 44 types of microbial rhodopsins from a cryptophyte flagellate, Guillardia theta. Due to the modest homology of amino acid sequences with a chlorophyte channelrhodopsin such as Cr_ChR2 from Chlamydomonas reinhardtii, it has been proposed that a family of cryptophyte channelrhodopsin, including Gt_CCR4, has a distinct molecular mechanism for channel gating and ion permeation. In this study, we compared the photocurrent properties, cation selectivity and kinetics between well-known Cr_ChR2 and Gt_CCR4 by a conventional path clamp method. Large and stable light-induced cation conduction by Gt_CCR4 at the maximum absorbing wavelength (530 nm) was observed with only small inactivation (15%), whereas the photocurrent of Cr_ChR2 exhibited significant inactivation (50%) and desensitization. The light sensitivity of Gt_CCR4 was higher (EC50 = 0.13 mW/mm2) than that of Cr_ChR2 (EC50 = 0.80 mW/mm2) while the channel open life time (photocycle speed) was in the same range as that of Cr_ChR2 (25~30 ms for Gt_CCR4 and 10~15 ms for Cr_ChR2). This observation implies that Gt_CCR4 enables optical neuronal spiking with weak light in high temporal resolution when applied in neuroscience. Furthermore, we demonstrated high Na+ selectivity of Gt_CCR4 in which the selectivity ratio for Na+ was 37-fold larger than that for Cr_ChR2, which primarily conducts H+. On the other hand, Gt_CCR4 conducted almost no H+ and no Ca2+ under physiological conditions. These results suggest that ion selectivity in Gt_CCR4 is distinct from that in Cr_ChR2. In addition, a unique red-absorbing and stable intermediate in the photocycle was observed, indicating a photochromic property of Gt_CCR4.

Increase rate of light-induced stomatal conductance is related to stomatal size in the genus Oryza.

The rapid response of stomatal conductance (gs) to fluctuating irradiance is of great importance to maximize carbon assimilation while minimizing water loss. Smaller stomata have been proven to have a faster response rate than larger ones, but most of these studies have been conducted with forest trees. In the present study, the effects of stomatal anatomy on the kinetics of gs and photosynthesis were investigated in 16 Oryza genotypes. Light-induced stomatal opening includes an initial time lag (λ) followed by an exponential increase. Smaller stomata had a larger maximum stomatal conductance increase rate (Slmax) during the exponential increase phase, but showed a longer time lag and a lower initial stomatal conductance (gs,initial) at low light. Stomatal size was, surprisingly, negatively correlated with the time required to reach 50% of maximum gs and photosynthesis (T50%gs and T50%A), which was shown to be positively correlated with λ and negatively correlated with gs,initial. With a lower gs,initial and a larger λ, small stomata showed a faster decrease of intercellular CO2 concentration (Ci) during the induction process, which may have led to a slower apparent Rubisco activation rate. Therefore, smaller stomata do not always benefit photosynthesis as reported before; the influence of stomatal size on dynamic photosynthesis is also correlated with λ and gs,initial.

Influences of acceptor dopants (Cu, Mg, Fe) on electrical and optical properties of Ba0.7Ca0.3TiO3 ceramics

Ba0.7Ca0.3TiO3 (BCT) ceramics with different dopants, including Fe3+, Mg2+, and Cu2+ ions, were prepared by a solid-state sintering method. All doping elements induced a change in the crystal structure and microstructure of BCT ceramics. The dielectric, ferroelectric and piezoelectric properties of the doped ceramics were observed in a correlation between the phase fraction and difference in grain size. The decrease of grain size indicated a surface enhancement in an ultraviolet light response of doped ceramics. The recovering rate of resistivity of all ceramics after removing the light depended on dopants. The results here suggested that microstructural variation could be useful for tuning both the electrical properties and ultraviolet light-induced conductivity of perovskite materials which may find future application in optoelectronic and electronic devices.

Substrate-Dependent Photoconductivity Dynamics in a High-Efficiency Hybrid Perovskite Alloy

Films of (FA$_{0.79}$MA$_{0.16}$Cs$_{0.05}$)$_{0.97}$Pb(I$_{0.84}$Br$_{0.16}$)$_{2.97}$ were grown over TiO$_{2}$, SnO$_{2}$, ITO, and NiO. Film conductivity was interrogated by measuring the in-phase and out-of-phase forces acting between the film and a charged microcantilever. We followed the films' conductivity vs. time, frequency, light intensity, and temperature (233 to 312 K). Perovskite conductivity was high and light-independent over ITO and NiO. Over TiO$_{2}$ and SnO$_{2}$, the conductivity was low in the dark, increased with light intensity, and persisted for 10's of seconds after the light was removed. At elevated temperature over TiO$_{2}$, the rate of conductivity recovery in the dark showed an activated temperature dependence (E$_{a}$ = 0.58 eV). Surprisingly, the light-induced conductivity over TiO$_{2}$ and SnO$_{2}$ relaxed essentially instantaneously at low temperature. We use a transmission-line model for mixed ionic-electronic conductors to show that the measurements presented are sensitive to the sum of electronic and ionic conductivities. We rationalize the seemingly incongruous observations using the idea that holes, introduced either by equilibration with the substrate or via optical irradiation, create iodide vacancies.

Energy-Resolved Photoconductivity Mapping in a Monolayer-Bilayer WSe2 Lateral Heterostructure.

Vertical and lateral heterostructures of van der Waals materials provide tremendous flexibility for band-structure engineering. Because electronic bands are sensitively affected by defects, strain, and interlayer coupling, the edge and heterojunction of these two-dimensional (2D) systems may exhibit novel physical properties, which can be fully revealed only by spatially resolved probes. Here, we report the spatial mapping of photoconductivity in a monolayer-bilayer WSe2 lateral heterostructure under multiple excitation lasers. As the photon energy increases, the light-induced conductivity detected by microwave impedance microscopy first appears along the heterointerface and bilayer edge, then along the monolayer edge, inside the bilayer area, and finally in the interior of the monolayer region. The sequential emergence of mobile carriers in different sections of the sample is consistent with the theoretical calculation of local energy gaps. Quantitative analysis of the microscopy and transport data also reveals the linear dependence of photoconductivity on the laser intensity and the influence of interlayer coupling on carrier recombination. Combining theoretical modeling, atomic-scale imaging, mesoscale impedance microscopy, and device-level characterization, our work suggests an exciting perspective for controlling the intrinsic band gap variation in 2D heterostructures down to a regime of a few nanometers.

Bidirectional light-induced conductance switching in molecular wires containing a dimethyldihydropyrene unit.

Photochromic coordination polymers, based on zinc(ii) bis-terpyridine-appended dimethyldihydropyrene building blocks, have been synthesized following stepwise synthesis on a surface yielding photo-switchable molecular junctions. Under irradiation, reversible structural changes occur by the isomerization of the photosensitive units, thus inducing conductance switching of the molecular junctions with a good reproducibility.

Light-induced Conductance Switching in Photomechanically Active Carbon Nanotube-Polymer Composites

Novel, optically responsive devices with a host of potential applications have been demonstrated by coupling carbon nanomaterials with photochromic molecules. For light-induced conductance switching in particular, we have recently shown that carbon nanotube-polymer nanocomposites containing azobenzene are very attractive and provide stable and non-degradable changes in conductivity over time at standard laboratory conditions. In these composites, the photoswitching mechanisms are based on light-induced changes in electronic properties and related to the Pool-Frenkel conduction mechanism. However, no link between conductivity switching and the molecular motion of azobenzene chromophores could be found due to application of high elastic modulus polymer matrices. Here we report on single wall carbon nanotube-polymer nanocomposites with a soft polycaprolactone polymer host. Such a system clearly shows the transfer of light-induced, nano-sized molecular motion to macroscopic thickness changes of the composite matrix. We demonstrate that these photomechanical effects can indeed overshadow the electronic effects in conductivity switching behavior and lead to a reversion of the conductivity switching direction near the percolation threshold.