A Cocatalyst that Stabilizes a Hydride Intermediate during Photocatalytic Hydrogen Evolution over a Rhodium-Doped TiO2 Nanosheet.

The hydrogen evolution reaction using semiconductor photocatalysts has been significantly improved by cocatalyst loading. However, there are still many speculations regarding the actual role of the cocatalyst. Now a photocatalytic hydrogen evolution reaction pathway is reported on a cocatalyst site using TiO2 nanosheets doped with Rh at Ti sites as one-atom cocatalysts. A hydride species adsorbed on the one-atom Rh dopant cocatalyst site was confirmed experimentally as the intermediate state for hydrogen evolution, which was consistent with the results of density functional theory (DFT) calculations. In this system, the role of the cocatalyst in photocatalytic hydrogen evolution is related to the withdrawal of photo-excited electrons and stabilization of the hydride intermediate species; the presence of oxygen vacancies induced by Rh facilitate the withdrawal of electrons and stabilization of the hydride.

Ni-Fe Nitride Nanoplates on Nitrogen-Doped Graphene as a Synergistic Catalyst for Reversible Oxygen Evolution Reaction and Rechargeable Zn-Air Battery.

Obtaining bifunctional electrocatalysts with high activity for the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) is a main hurdle in the application of rechargeable metal-air batteries. Earth-abundant 3d transition metal-based catalysts have been developed for the OER and ORR; however, most of these are based on oxides, whose insulating nature strongly restricts their catalytic performance. This study describes a metallic Ni-Fe nitride/nitrogen-doped graphene hybrid in which 2D Ni-Fe nitride nanoplates are strongly coupled with the graphene support. Electronic structure of the Ni-Fe nitride is changed by hybridizing with the nitrogen-doped graphene. The unique heterostructure of this hybrid catalyst results in very high OER activity with the lowest onset overpotential (150 mV) reported, and good ORR activity comparable to that for commercial Pt/C. The high activity and durability of this bifunctional catalyst are also confirmed in rechargeable zinc-air batteries that are stable for 180 cycles with an overall overpotential of only 0.77 V at 10 mA-2 .

Application to Photocatalytic H2 Production of a Whole-Cell Reaction by Recombinant Escherichia coli Cells Expressing [FeFe]-Hydrogenase and Maturases Genes.

A photocatalytic H2 production system using an inorganic-bio hybrid photocatalyst could contribute to the efficient utilization of solar energy, but would require the development of a new approach for preparing a H2 -forming biocatalyst. In the present study, we constructed a recombinant strain of Escherichia coli expressing the genes encoding the [FeFe]-hydrogenase and relevant maturases from Clostridium acetobutylicum NBRC 13948 for use as a biocatalyst. We investigated the direct application of a whole-cell of the recombinant E. coli. The combination of TiO2 , methylviologen, and the recombinant E. coli formed H2 under light irradiation, demonstrating that whole cells of the recombinant E. coli could be employed for photocatalytic H2 production without any time-consuming and costly manipulations (for example, enzyme purification). This is the first report of the direct application of a whole-cell reaction of recombinant E. coli to photocatalytic H2 production.

Synthesis and Investigation of the Effect of Substitution on the Structure, Physical Properties, and Electrochemical Properties of Anthracenodifuran Derivatives.

A series of syn/anti mixtures of anthradifuran (ADF) and substituent compounds were systematically synthesized, and the effect of substitution at the 5,11-positions on the neutral and radical states of ADF was investigated. All compounds were measured and analyzed by absorption and fluorescence spectroscopy, cyclic voltammetry, electrochemical absorption spectroscopy, and DFT calculations. The absorption spectra of 5,11-substituent compounds in their neutral state were red-shifted. In addition, the substituted compounds exhibited increased thermal stability with respect to the parent 1a because of elongation of the π-conjugation and an increased steric hindrance effect due to the bulky ethynyl substituent groups. The cyclic voltammograms of all of the compounds exhibited irreversible reduction potentials and irreversible oxidation potentials, except in the case of (trimethylsilyl)silylethynyl-substituted ADF. When the materials were subjected to oxidation/reduction potentials, the radical cation and anion species were generated. The absorption spectra of the radical-cation species of the compounds exhibited similar characteristics and similar absorption ranges (550-1400 nm), whereas the spectra of the radical anion species were blue-shifted (550-850 nm) compared than that of the parent 1a(•-) (550-1100 nm). The DFT computation results suggested that the radical states of lowest energy transitions occurred primarily from π to π(SOMO) or from π(SOMO) to π*.

Direct imaging of light emission centers in two-dimensional crystals and their luminescence and photocatalytic properties.

To fully understand the fundamental properties of light-energy-converting materials, it is important to determine the local atomic configuration of photofunctional centers. In this study, direct imaging of one- and two-Tb-atom emission centers in a two-dimensional Tb-doped Ca2Ta3O10 nanocrystal was carried. The emission centers were located at the Ca sites in the perovskite structure, and no concentration-based quenching was observed even when the emission centers were in close proximity to each other. The relative photoluminescence efficiency for green emission of the nanosheet suspension was 38.1%. Furthermore, the Tb-doped Ca2Ta3O10 nanocrystal deposited co-catalyst showed high photocatalytic activity for hydrogen production from water (quantum efficiency: 71% at 270 nm). Tb(3+) dopants in the two-dimensional crystal might have the potential to stabilize the charge separation state.

Modification effects of meso-hexakis(pentafluorophenyl) [26]hexaphyrin aggregates on the photocatalytic water splitting.

Water splitting activity of a GaN:ZnO photocatalyst was improved by meso-hexakis(pentafluorophenyl) [26]hexaphyrin (3). The hexaphyrin (3) assisted the water splitting reaction over the GaN:ZnO photocatalyst by using visible light energy around 600 nm.

Potential gradient and photocatalytic activity of an ultrathin p-n junction surface prepared with two-dimensional semiconducting nanocrystals.

The creation of p-n junction structure in photocatalysts is a smart approach to improve the photocatalytic activity, as p-n junctions can potentially act to suppress the recombination reaction. Understanding the surface conditions of the junction parts is one of the biggest challenges in the development of photocatalyst surface chemistry. Here, we show a relationship between the photocatalytic activity and potential gradient of the junction surface prepared from two-dimensional crystals of p-type NiO and n-type calcium niobate (CNO). The ultrathin (ca. 2 nm) junction structure and the surface potential were analyzed using low energy ion scattering spectroscopy and Kelvin probe force microscopy. The photocatalytic H2 production rate for the n-p (CNO/NiO) junction surface was higher than those for p-n (NiO/CNO) junction, p, and n surfaces. The surface potential of the CNO/NiO junction part (surface: CNO) was lower than that of the CNO crystals in the same CNO crystal surface. These potential gradients result in specially separated reaction sites, which suppress the recombination reaction in the CNO nanosheet. Photo-oxidation and photoreduction sites in the junction structure were confirmed using the photodeposition reaction of MnO(x) and Ag.

One-pot soft-templating method to synthesize crystalline mesoporous tantalum oxide and its photocatalytic activity for overall water splitting.

Crystalline mesoporous Ta2O5 has been successfully synthesized by a one-pot route using P-123 as the structure directing agent (SDA). A series of crystalline mesoporous Ta2O5 samples has been prepared by changing the calcination temperature. The surface area decreased and the pore size increased with the increasing calcination temperature, which were the results of crystallite growth. At the same time, the pore volume was well maintained, which means limited shrinkage during the calcination of elevated temperature. The porous structure and crystal structure of as-synthesized mesoporous Ta2O5 were characterized by XRD, TG-DTA, SEM, TEM, and N2 sorption techniques. The photocatalytic activity of the as-synthesized mesoporous Ta2O5 with the cocatalyst NiOx for overall water splitting under ultraviolet (UV) light irradiation was systematically evaluated. The photocatalytic activity of crystalline mesoporous Ta2O5 showed about 3 times that of commercial Ta2O5 powder and 22 times that of amorphous mesoporous Ta2O5.

Preparation of tantalum-based oxynitride nanosheets by exfoliation of a layered oxynitride, CsCa2Ta3O(10-x)N(y), and their photocatalytic activity.

Calcium tantalum oxynitride [Ca(2)Ta(3)O(9.7)N(0.2)](-) nanosheets were prepared by exfoliating a layered perovskite oxynitride (CsCa(2)Ta(3)O(9.7)N(0.2)) via proton exchange and two-step intercalation of ethylamine and tetrabutylammonium ions. Monolayer nanosheet was prepared by the above processes, although some bilayer or trilayer nanosheets were also produced. The [Ca(2)Ta(3)O(9.7)N(0.2)](-) nanosheets exhibited photocatalytic activity for H(2) evolution from water under visible light irradiation. In contrast, CsCa(2)Ta(3)O(9.7)N(0.2) exhibited very low photocatalytic activity for H(2) evolution under the visible light irradiation, even when methanol was added to water as a sacrificial agent. The improved photocatalytic activity originates from the characteristics of nanosheets such as their molecular thickness and large surface area. Further, the Rh-loaded [Ca(2)Ta(3)O(9.7)N(0.2)](-) nanosheets restacked with protons exhibited photocatalytic activity for H(2) and O(2) evolution from pure water under UV-light irradiation. The ratio of H(2)/O(2) evolved was around 3. The ratio of N/O in the catalyst remained the same after the photocatalytic reaction, signifying that there was no decomposition of the catalyst during the reaction. This indicates that the present N-doped nanosheet is stable in the photocatalytic reaction.

Synthesis and photocatalytic activity of rhodium-doped calcium niobate nanosheets for hydrogen production from a water/methanol system without cocatalyst loading.

Rhodium-doped calcium niobate nanosheets were synthesized by exfoliating layered KCa(2)Nb(3-x)Rh(x)O(10-δ) and exhibited high photocatalytic activity for H(2) production from a water/methanol system without cocatalyst loading. The maximum H(2) production rate of the nanosheets was 165 times larger than that of the parent Rh-doped layered oxide. The quantum efficiency at 300 nm was 65%. In this system, the methanol was oxidized to formaldehyde (main product), formic acid, and carbon dioxide by holes, whereas electrons cause the reduction of water to H(2). The conductivity of the parent layered oxide was decreased by doping, which indicates the octahedral RhO(6) unit in the lattice of the nanosheet functions as an electron trap site. The RhO(6) units in the nanosheet probably also act as reaction sites for H(2) evolution.

Long-time charge separation in porphyrin/KTa(Zr)O3 as water splitting photocatalyst.

Artificial photosynthesis is one of the chemists' dreams and the separation of charges with long lives is fundamental for achieving artificial photosynthesis. In actual photosynthesis, Z-scheme excitation separates electronic charge with high efficiency using solar light. Here we report that photo-excitation in Cr-tetraphenylporphyrin chroride (Cr-TPPCl)/Zr doped KTaO(3) (KTa(Zr)O(3)) is analogous to the Z-scheme in photosynthesis, and that we achieve complete charge separation at room temperature. Photovoltaic decay and transient fluorescence spectra measurements showed that the photo-excited charge in KTa(Zr)O(3) transferred to the HOMO of Cr-TPPCl within a few hundred pico-seconds on charge transfer. In contrast, the reduced state of the Cr-TPPCl species that was formed by the electronic injection from KTa(Zr)O(3) was observed for more than 0.5 s at room temperature in the transient decay of the absorption spectra change after the initial excitation of KTa(Zr)O(3). The formed reduced state of Cr-TPPCl was highly stable and was detected by static ESR measurements.

Preparation of p-type CaFe2O4 photocathodes for producing hydrogen from water.

An (hk0)-oriented p-type CaFe2O4 (E(g): 1.9 eV) photocathode was prepared, and hydrogen and oxygen gases were produced from a photocell short-circuited by connecting the CaFe2O4 and n-type TiO2 electrodes under illumination without applying an external voltage. The open-circuited voltage was 0.97 V and the short-circuit current was about 200 µA/cm(2), and the amount of evaluated hydrogen and oxygen gases after 2 days of reaction were about 70 and 4 µmol, respectively.

Charge-transfer mechanism in Pt/KTa(Zr)O(3) photocatalysts modified with porphyrinoids for water splitting.

The mechanism of photocatalytic splitting of H(2)O into H(2) and O(2) on Pt/KTa(Zr)O(3) modified with various porphyrinoids was investigated. The photocatalytic activity of KTaO(3) catalysts is improved by dye modification. Cyanocobalamin (vitamin B(12)) is the most effective for improving water-splitting activity, and the formation rates of H(2) and O(2) achieved values of 575 and 280 micromol g(cat.) (-1) h(-1), respectively. X-ray photoelectron spectroscopy spectra of KTa(Zr)O(3) photocatalysts showed that Pt loaded onto dye-modified KTaO(3) was slightly oxidized and had low catalytic activity for the H(2) oxidation reaction. Photoluminescence (PL) spectra of KTaO(3) catalysts suggested that excitation energy was transferred between KTaO(3), tetraphenylporphyrinatochromium(III) (Cr-TPP), and the Pt cocatalyst. The wavelength dependence of the activity of dye-modified KTa(Zr)O(3) photocatalysts indicated that excitation of both KTa(Zr)O(3) and the dye was essential for achieving increased photocatalytic activity. This result suggests that two-step excitation occurred in the dye-modified KTa(Zr)O(3) photocatalysts. Because the lifetime of the charge-separated state increased, this study reveals that modification with porphyrinoids is effective for increasing water-splitting activity.