Charge Trapping in Semiconductor Photocatalysts: A Time- and Space-Domain Perspective.

Harnessing solar energy to produce value-added fuels and chemicals through photocatalysis techniques holds promise for establishing a sustainable and environmentally friendly energy economy. The intricate dynamics of photogenerated charge carriers lies at the core of the photocatalysis. The balance between charge trapping and band-edge recombination has a crucial influence on the activity of semiconductor photocatalysts. Consequently, the regulation of traps in photocatalysts becomes the key to optimizing their activities. Nevertheless, our comprehension of charge trapping, compared to that of well-studied charge recombination, remains somewhat limited. This limitation stems from the inherently heterogeneous nature of traps at both temporal and spatial scales, which renders the characterization of charge trapping a formidable challenge. Fortunately, recent advancements in both time-resolved spectroscopy and space-resolved microscopy have paved the way for considerable progress in the investigation and manipulation of charge trapping. In this Perspective, we focus on charge trapping in photocatalysts with the aim of establishing a direct link to their photocatalytic activities. To achieve this, we begin by elucidating the principles of advanced time-resolved spectroscopic techniques such as femtosecond time-resolved transient absorption spectroscopy and space-resolved microscopic methods, such as single-molecule fluorescence microscopy and surface photovoltage microscopy. Additionally, we provide an overview of noteworthy research endeavors dedicated to probing charge trapping using time- and space-resolved techniques. Our attention is then directed toward recent achievements in the manipulation of charge trapping in photocatalysts through defect engineering. Finally, we summarize this Perspective and discuss the future challenges and opportunities that lie ahead in the field.

Size-Controlled Synthesis of Luminescent Few-Atom Silver Clusters via Electron Transfer in Isostructural Redox-Active Porous Ionic Crystals.

Ag clusters with a controlled number of atoms have received significant interest because they show size-dependent catalytic, optical, electronic, or magnetic properties. However, the synthesis of size-controlled, ligand-free, and air-stable Ag clusters with high yields has not been well-established. Herein, it is shown that isostructural porous ionic crystals (PICs) with redox-active polyoxometalates (POMs) can be used to synthesize Ag clusters via electron transfer from POMs to Ag+ . Ag clusters with average numbers of three, four, or six atoms emitting blue, green, or red colors, respectively, are formed and stabilized in the PICs under ambient conditions without any protecting ligands. The cluster size solely correlates with the degree of electron transfer, which is controlled by the reduction time and types of ions or elements of the PICs. Thus, advantages have been taken of POMs as electron sources and PICs as scaffolds to demonstrate a convenient method to obtain few-atom Ag clusters.

Mechanochromic Luminescence (MCL) of Purely Organic Two-Component Dyes: Wide-Range MCL over 300†nm and Two-Step MCL by Charge-Transfer Complexation.

Despite recent extensive studies on mechanochromic luminescence (MCL), rational control over the magnitude of the emission-wavelength shift in response to mechanical stimuli remains challenging. In the present study, a two-component donor-acceptor approach has been applied to create a variety of organic MCL composites that exhibit remarkable emission-wavelength switching. Dibenzofuran-based bis(1-pyrenylmethyl)diamine and typical organic fluorophores have been employed as donor and acceptor dyes, respectively. Outstanding wide-range MCL with an emission-wavelength shift of over 300 nm has been achieved by mixing the diamine with 3,4,9,10-perylenetetracarboxylic diimide. Unprecedented two-step MCL in response to mechanical stimuli of different intensity has also been realized for a two-component mixture with 9,10-anthraquinone. Fluorescence microscopy observations at the single-particle level revealed that the segregation and mixing of the two-component dyes contribute to the stimuli-responsive emission-color switching of the MCL composites.

In Situ Exploration of the Structural Transition during Morphology- and Efficiency-Conserving Halide Exchange on a Single Perovskite Nanocrystal.

Controlled fabrication of semiconductor nanostructures with unique physicochemical properties is vital for future technologies. In this study, transformation from red-emitting metal halide perovskite CH3 NH3 PbI3 nanocrystals (NCs) to green-emitting CH3 NH3 PbBr3 NCs was achieved without significant morphological changes and loss of photoluminescence (PL) efficiency via a controlled halide exchange reaction. In situ single-particle PL imaging along with detailed structural and elemental characterizations revealed that sudden cooperative transitions between two light-emitting states via intermediate dark states with >100 s durations during halide exchange originate from two distinct defect-mediated reconstruction processes with different activation energies (0.072 and 0.40 eV), leading to an isokinetic temperature of ca. 314 K, across a solid-state miscibility gap between the I- and Br-rich phases inside a single NC.

Ultra-Narrow Depletion Layers in a Hematite Mesocrystal-Based Photoanode for Boosting Multihole Water Oxidation.

Significant charge recombination that is difficult to suppress limits the practical applications of hematite (α-Fe2 O3 ) for photoelectrochemical water splitting. In this study, Ti-modified hematite mesocrystal superstructures assembled from highly oriented tiny nanoparticle (NP) subunits with sizes of ca. 5 nm were developed to achieve the highest photocurrent density (4.3 mA cm-2 at 1.23 V vs. RHE) ever reported for hematite-based photoanodes under back illumination. Owing to rich interfacial oxygen vacancies yielding an exceedingly high carrier density of 4.1×1021  cm-3 for super bulk conductivity in the electrode and a large proportion of ultra-narrow depletion layers (<1 nm) inside the mesoporous film for significantly improved hole collection efficiency, a boosting of multihole water oxidation with very low activation energy (Ea =44 meV) was realized.

The Development of Functional Mesocrystals for Energy Harvesting, Storage, and Conversion.

Higher-ordered semiconductors have attracted extensive research interest as an adopted engineering for active solar energy harvesting, storage, and conversion. It is well-known that the effective separation and anisotropic migration of photogenerated charges are the basic driven force required for superior efficiency. However, the morphology and stoichiometric variation of these semiconductors play essential roles in their physicochemical properties of bulk and surface, especially for efficient interparticle or interfacial charge transfer. To this point, the strategy of controlling the topotactic transformation toward superstructures with optimized functionality is preferable for a wide range of optoelectronic and catalytic engineering applications. In this Minireview, we provide an overview of the crystal orientation, synthetic engineering, functional applications, and spatial and temporal charge dynamics in TiO2 mesocrystals and others. The viewpoint of in-depth understanding of the structure-related kinetics would offer an opportunity for design of versatile mesocrystal semiconductors sought-after for potential applications.

Topotactic Epitaxy of SrTiO3 Mesocrystal Superstructures with Anisotropic Construction for Efficient Overall Water Splitting.

The higher-order structures of semiconductor-based photocatalysts play crucial roles in their physicochemical properties for efficient light-to-energy conversion. A novel perovskite SrTiO3 mesocrystal superstructure with well-defined orientation of assembled cubic nanocrystals was synthesized by topotactic epitaxy from TiO2 mesocrystals through a facile hydrothermal treatment. The SrTiO3 mesocrystal exhibits three times the efficiency for the hydrogen evolution of conventional disordered systems in alkaline aqueous solution. It also exhibits a high quantum yield of 6.7 % at 360 nm in overall water splitting and even good durability up to 1 day. Temporal and spatial spectroscopic observations revealed that the synergy of the efficient electron flow along the internal nanocube network and efficient collection at the larger external cubes produces remarkably long-lived charges for enhanced photocatalysis.

Geometries, Electronic Couplings, and Hole Dissociation Dynamics of Photoinduced Electron-Hole Pairs in Polyhexylthiophene-Fullerene Dyads Rigidly Linked by Oligophenylenes.

To shed a light on fundamental molecular functions of photoinduced charge conductions by organic photovoltaic materials, it is important to directly observe molecular geometries of the intermediate charges just after the photoinduced electron-transfer reactions. However, highly inhomogeneous molecular environments at the bulk heteojunction interfaces in the photoactive layers have prevented us from understanding the mechanism of the charge conductions. We have herein investigated orbital geometries, electronic couplings, and hole-dissociation dynamics of photoinduced charge-separated (CS) states in a series of poly(3-hexylthiophene)-fullerene linked dyads bridged by rigid oligo-p-phenylene spacers by using time-resolved EPR spectroscopy. It has been revealed that one-dimensional intramolecular hole-dissociations exothermically take place from localized holes in initial CS states, following bridge-mediated, photoinduced charge-separations via triplet exciton diffusions in the conjugated polymer-backbones. This molecular wire property of the photoinduced charges in solution at room temperature demonstrates the potential utility of the covalently bridged polymer molecules applied for the molecular devices.

Plasmon-enhanced formic acid dehydrogenation using anisotropic Pd-Au nanorods studied at the single-particle level.

Plasmonic bimetal nanostructures can be used to drive the conventional catalytic reactions efficiently at low temperature with the utilization of solar energy. This work developed Pd-modified Au nanorods, which work as the light absorber and the catalytically active site simultaneously, and exhibit efficient plasmon-enhanced catalytic formic acid dehydrogenation even when below room temperature (5 °C). Plasmon-induced interface interaction and photoreaction dynamics of individual nanorods were investigated by single-particle photoluminescence measurement, and a complete quenching phenomenon at the LSPR region was observed for the first time. More importantly, the spatial distribution of the SPR-induced enhancement, analyzed by the finite difference time domain (FDTD) simulation, shows that only tip-coated Pd can be affected for the occurrence of plasmon resonance energy transfer. This finding provides a route to decrease the amount of Pd species by the selective deposition only at the field-enhanced sites.

Atomically engineered metal-insulator transition at the TiO2/LaAlO3 heterointerface.

We demonstrate that the atomic boundary conditions of simple binary oxides can be used to impart dramatic changes of state. By changing the substrate surface termination of LaAlO3 (001) from AlO2 to LaO, the room-temperature sheet conductance of anatase TiO2 films are increased by over 3 orders of magnitude, transforming the intrinsic insulating state to a high mobility metallic state, while maintaining excellent optical transparency.

Single-particle study of Pt-modified Au nanorods for plasmon-enhanced hydrogen generation in visible to near-infrared region.

Pt-modified Au nanorods (NRs) synthesized by anisotropic overgrowth were used for producing H2 under visible and near-infrared light irradiation. The Pt-tipped sample exhibited much higher activity compared with fully covered samples. Using single-particle spectroscopies combined with transmission electron microscopy, we observed obvious quenching phenomena for photoluminescence and light scattering from individual Pt-tipped NRs. The analysis of energy relaxation of plasmon-generated hot electrons indicates the electron transfer from the excited Au to Pt.

Au/TiO2 superstructure-based plasmonic photocatalysts exhibiting efficient charge separation and unprecedented activity.

Plasmonic photocatalysts were successfully synthesized by the modification of TiO2 mesocrystals with Au nanoparticles (NPs) by a simple impregnation method. The Au NP sensitizers show a strong photoelectrochemical response in the visible-light region (400-800 nm) due to their surface plasmon resonance (SPR). The diffuse reflectance spectroscopy measurements on a wide range of time scales (from picoseconds to minutes) demonstrate that a substantial part of electrons, injected from the Au NPs to the TiO2 mesocrystals through the SPR excitation, directionally migrate from the basal surfaces to the edges of the plate-like mesocrystals through the TiO2 nanocrystal networks and are temporally stored there for further reactions. This anisotropic electron flow significantly retarded the charge recombination of these electrons with the holes in the Au NPs, thereby improving the visible-light-photocatalytic activity (for organic-pollutant degradation) by more than an order of magnitude, as compared to that of conventional Au/TiO2 NP systems.

Far-red fluorescence probe for monitoring singlet oxygen during photodynamic therapy.

Singlet oxygen ((1)O2), molecular oxygen in the lowest excited state, has a critical role in the cell-killing mechanism of photodynamic therapy (PDT). Although (1)O2 phosphorescence measurement has been mainly used to monitor (1)O2 formation during PDT, its intensity is far insufficient to obtain two-dimensional images of intracellular (1)O2 with the subcellular spatial resolution using the currently available near-IR detector. Here, we propose a new far-red fluorescence probe of (1)O2, namely, Si-DMA, composed of silicon-containing rhodamine and anthracene moieties as a chromophore and a (1)O2 reactive site, respectively. In the presence of (1)O2, fluorescence of Si-DMA increases 17 times due to endoperoxide formation at the anthracene moiety. With the advantage of negligible self-oxidation by photoirradiation (ΦΔ < 0.02) and selective mitochondrial localization, Si-DMA is particularly suitable for imaging (1)O2 during PDT. Among three different intracellular photosensitizers (Sens), Si-DMA could selectively detect the (1)O2 that is generated by 5-aminolevulinic acid-derived protoporphyrin IX, colocalized with Si-DMA in mitochondria. On the other hand, mitochondria-targeted KillerRed and lysosomal porphyrins could not induce fluorescence change of Si-DMA. This surprising selectivity of Si-DMA response depending on the Sens localization and photosensitization mechanism is caused by a limited intracellular (1)O2 diffusion distance (∼300 nm) and negligible generation of (1)O2 by type-I Sens, respectively. For the first time, we successfully visualized (1)O2 generated during PDT with a spatial resolution of a single mitochondrial tubule.

Molecular-level understanding of the photocatalytic activity difference between anatase and rutile nanoparticles.

The generation of oxidants on illuminated photocatalysts and their participation in subsequent reactions are the main basis of the widely investigated photocatalytic processes for environmental remediation and selective oxidation. Here, the generation and the subsequent diffusion of (·)OH from the illuminated TiO2 surface to the solution bulk were directly observed using a single-molecule detection method and this molecular phenomenon could explain the different macroscopic behavior of anatase and rutile in photocatalysis. The mobile (·)OH is generated on anatase but not on rutile. Therefore, the photocatalytic oxidation on rutile is limited to adsorbed substrates whereas that on anatase is more facile and versatile owing to the presence of mobile (·)OH. The ability of anatase to generate mobile (·)OH is proposed as a previously unrecognized key factor that explains the common observations that anatase has higher activity than rutile for many photooxidative reactions.

Intricate Reaction Pathways on CH3NH3PbI3 Photocatalysts in Aqueous Solution Unraveled by Single-Particle Spectroscopy.

Organic-inorganic hybrid perovskites such as MAPbI3 (MA+ = CH3NH3+) have emerged as promising materials for solar cells and light-emitting devices. Despite their poor stability against moisture, perovskites work as hydrogen-producing photocatalysts or photosensitizers in perovskite-saturated aqueous solutions. However, the fundamental understanding of how chemical species or support materials in the solution affect the dynamics of the photogenerated charges in perovskites is still insufficient. In this study, we investigated the photoluminescence (PL) properties of MAPbI3 nanoparticles in aqueous media at the single-particle level. A remarkable PL blinking phenomenon, along with significant decreases in the PL intensity and lifetime compared to those in ambient air, suggested temporal fluctuations in the trapping rates of photogenerated holes by chemical species (I- and H3PO2) in the solution. Moreover, electron transfer from the excited MAPbI3 to Pt-modified TiO2 proceeds in a concerted fashion for photocatalytic hydrogen evolution under the dynamic solid-solution equilibrium condition.

Single-molecule, single-particle approaches for exploring the structure and kinetics of nanocatalysts.

In this Article, we focus on the in situ observation of photochemical reactions on individual nanoobjects of solid catalysts using single-molecule, single-particle fluorescence spectroscopy. The use of high-resolution imaging techniques with suitable fluorogenic probes enables us to determine the location of the catalytically active sites that are related to the structural heterogeneities on the surface of the solid catalyst and the temporal fluctuation of photochemical reactivity. Furthermore, we present the real-time observation of metastable gold nanoclusters in polymer matrices at the single-cluster level. This Article encourages readers to explore the nanoworld in terms of practical applications in many fields such as fundamental physics and chemistry.

Selective oxidative degradation of organic pollutants by singlet oxygen-mediated photosensitization: tin porphyrin versus C60 aminofullerene systems.

This study evaluates the potential application of tin porphyrin- and C(60) aminofullerene-derivatized silica (SnP/silica and aminoC(60)/silica) as (1)O(2) generating systems for photochemical degradation of organic pollutants. Photosensitized (1)O(2) production with SnP/silica, which was faster than with aminoC(60)/silica, effectively oxidized a variety of pharmaceuticals. Significant degradation of pharmaceuticals in the presence of the 400-nm UV cutoff filter corroborated visible light activation of both photosensitizers. Whereas the efficacy of aminoC(60)/silica for (1)O(2) production drastically decreased under irradiation with λ > 550 nm, Q-band absorption caused negligible loss of the photosensitizing activity of SnP/silica in the long wavelength region. Faster destruction of phenolates by SnP/silica and aminoC(60)/silica under alkaline pH conditions further implicated (1)O(2) involvement in the oxidative degradation. Direct charge transfer mediated by SnP, which was inferred from nanosecond laser flash photolysis, induced significant degradation of neutral phenols under high power light irradiation. Self-sensitized destruction caused gradual activity loss of SnP/silica in reuse tests unlike aminoC(60)/silica. The kinetic comparison of SnP/silica and TiO(2) photocatalyst in real wastewater effluents showed that photosensitized singlet oxygenation of pharmaceuticals was still efficiently achieved in the presence of background organic matters, while significant interference was observed for photocatalyzed oxidation involving non-selective OH radical.

Interfacial electron transfer dynamics in dye-modified graphene oxide nanosheets studied by single-molecule fluorescence spectroscopy.

Graphene oxide (GO) nanosheets have received a great deal of attention for a wide range of applications from optoelectronic devices to biological sensors. We now report a mechanistic study of the interfacial electron transfer (ET) processes between organic dye molecule, 9-phenyl-2,3,7-trihydroxy-6-fluorone (PF), and nanometre-sized GO sheets using ensemble-averaged and single-molecule spectroscopies. The ET dynamics was characterized by the direct observation of the PF radical cation during the laser flash photolysis, and its reaction rate was determined to be ~10(11) s(-1). The single-molecule fluorescence spectroscopy was utilized to clarify the heterogeneous nature of the interfacial ET within individual composites. Their fluorescence lifetimes and spectra were found to vary from composite to composite, possibly due to the different local structures and molecular interactions. The autocorrelation analysis of fluorescence intensity trajectories also revealed the temporal fluctuation of the ET reactivity.

Extension of the mechanoresponsive luminescence shift via formation of a doped organic crystal.

Herein, we propose a new strategy to tune the magnitude of the mechanoresponsive shift of the maximum emission wavelength (Δλem). The Δλem of thienylbenzothiadiazole crystals has been extended to 69 nm by doping with a trace amount of dithienylbenzothiadiazole, whereas the pure crystal of thienylbenzothiadiazole exhibited a Δλem of 10 nm. This doping strategy should accelerate the development of advanced mechanosensing materials composed of organic crystals.

Binary dopant segregation enables hematite-based heterostructures for highly efficient solar H2O2 synthesis.

Dopant segregation, frequently observed in ionic oxides, is useful for engineering materials and devices. However, due to the poor driving force for ion migration and/or the presence of substantial grain boundaries, dopants are mostly confined within a nanoscale region. Herein, we demonstrate that core-shell heterostructures are formed by oriented self-segregation using one-step thermal annealing of metal-doped hematite mesocrystals at relatively low temperatures in air. The sintering of highly ordered interfaces between the nanocrystal subunits inside the mesocrystal eliminates grain boundaries, leaving numerous oxygen vacancies in the bulk. This results in the efficient segregation of dopants (~90%) on the external surface, which forms their oxide overlayers. The optimized photoanode based on hematite mesocrystals with oxide overlayers containing Sn and Ti dopants realises high activity (~0.8 µmol min-1 cm-2) and selectivity (~90%) for photoelectrochemical H2O2 production, which provides a wide range of application for the proposed concept.