Physicochemical insights into semiconductor properties of a semitransparent tantalum nitride photoanode for solar water splitting.

The self-conductivity of tantalum nitride (Ta3N5) thin film-based semitransparent photoanodes was found to promote the current originating from the photoelectrochemical oxygen evolution reaction (PEC OER) without a conducting substrate. With surface modification by the NiFeOx-electrocatalyst, an optimized Ta3N5 thin film fabricated directly on a transparent insulating quartz substrate generated a photocurrent density of ∼5.9 ± 0.1 mA cm-2 at 1.23 V vs. the reversible hydrogen electrode under simulated AM 1.5G solar illumination. The correlation between the PEC OER performance of NiFeOx-modified Ta3N5 photoanodes and the electrical properties of Ta3N5 thin films was investigated based on the Hall effect measurements. By changing the nitridation conditions, these properties can be tuned so that the higher the Hall mobility (0.2 to 1.7 cm2 V-1 s-1) and the lower the carrier concentration (1020 to 1019 cm-3). The surface chemical states of Ta3N5 thin films were investigated using X-ray photoelectron spectroscopy as a means of evaluating surface oxygen impurities and nitrogen vacancies, which may correlate with the PEC OER performance and the electrical properties of the material.

Exploring the Photocorrosion Mechanism of a Photocatalyst.

Photoelectrochemical (PEC) water splitting using Ta3N5 anodes shows a high solar-to-hydrogen (STH) efficiency approaching 10%. However, the long-term stability of gas evolution should be improved for the commercial utilization of PEC water-splitting technology. Herein, we examined the photocurrent degradation of photoanodes prepared by uniformly loading a NiFeOx cocatalyst onto a Ta3N5 semiconductor. Although spectroscopic analysis showed that the degradation was attributable to the formation of an oxide layer, several oxide growth kinetic laws and mechanisms are known. We theoretically derived the photocurrent kinetic laws instead of the oxide growth kinetic laws by generalizing the Cabrera-Mott oxidation theory of metal oxidation in air to apply it to photocorrosion. The measured photocurrent kinetics are fully consistent with the theoretical kinetic laws. We show that ion drift due to charging of the oxide layer limits oxide growth even though uniform cocatalyst loading is designed to prevent self-oxidation of Ta3N5.

Maximizing Oxygen Evolution Performance on a Transparent NiFeOx/Ta3N5 Photoelectrode Fabricated on an Insulator.

A transparent Ta3N5 photoanode is a promising candidate for the front-side photoelectrode in a photoelectrochemical (PEC) cell with tandem configuration (tandem cell), which can potentially provide high solar-to-hydrogen (STH) energy conversion efficiency. This study focuses in particular on the semiconductor properties and interfacial design of transparent Ta3N5 photoanodes fabricated on insulating quartz substrates (Ta3N5/SiO2), typically the geometric area of 1 × 1 cm2 in contact with indium on its edge. This material utilizes the self-conductivity of Ta3N5 to make the PEC system operational, and the electrode would strongly reflect the intrinsic nature of Ta3N5 without a back contact that is commonly introduced. First, PEC measurements using acetonitrile (ACN)/H2O mixed solution were made to elucidate the intrinsic photoresponse in the presence of tris(2,2'-bipyridine)ruthenium(II) bis(hexafluorophosphate) (Ru(bpy)3(PF6)2) without water contact which avoids a multielectron-transfer oxygen evolution reaction (OER) and photoinduced self-oxidation. The potential difference between the onset potential of Ru2+ PEC oxidation by Ta3N5/SiO2 and the redox potential of Ru2+/3+ in the nonaqueous environment was about 0.7 V. While a stable photoanodic response was observed for Ta3N5/SiO2 in the nonaqueous phase, the addition of a small quantity of water into this nonaqueous system led to the immediate deactivation of Ta3N5/SiO2 photoanode under illumination by self-photooxidation to form TaOx at the solid/water interface. In aqueous phase, flatband potentials estimated from Mott-Schottky analysis varied with solution pH (constant potential against reversible hydrogen electrode (RHE)). Photoelectrode modification by a transparent NiFeOx layer was attempted. The complete coverage of the Ta3N5 surface with transparent NiFeOx electrocatalysts, achieved by an optimized spin-coating protocol with controlled Ni-Fe precursors, allowed for the successful protection of Ta3N5 and demonstrated an extremely stable photocurrent for hours without any additional protective layers. The stability of the resultant NiFeOx/Ta3N5/SiO2 was limited not by Ta3N5 but mainly by a NiFeOx electrocatalyst due to Fe dissolution with time.

Efficient Water Oxidation Using Ta3 N5 Thin Film Photoelectrodes Prepared on Insulating Transparent Substrates.

Photoelectrochemical (PEC) water splitting using visible-light-responsive photoelectrodes is the preferred approach to converting solar energy into hydrogen as a renewable energy source. A transparent Ta3 N5 photoanode embedded within a PEC cell having a tandem configuration is a promising configuration that may provide a high solar-to-hydrogen energy conversion efficiency. Ta3 N5 thin films are typically prepared by heating precursor films in an NH3 flow at high temperatures, which tends to degrade the transparent conductive layer, such that producing efficient Ta3 N5 transparent photoanodes is challenging. Herein, the direct preparation of transparent Ta3 N5 photoanodes on insulating quartz substrates was demonstrated without the insertion of a transparent conductive layer. The resulting devices generated a photocurrent of 6.0 mA cm-2 at 1.23 V vs. a reversible hydrogen electrode under simulated sunlight. This study provides a new strategy for the preparation of transparent photoelectrodes that mitigates current challenges.

Ti cluster-alkylated hydrophobic MOFs for photocatalytic production of hydrogen peroxide in two-phase systems.

A hydrophobic MOF, OPA/MIL-125-NH2, whose Ti cluster was alkylated with octadecylphosphonic acid (OPA), was found to enhance photocatalytic H2O2 production in a two-phase system. Its activity exceeded that of linker-alkylated MIL-125-NH2. OPA/MIL-125-NH2 was modified on its outermost surface, which resulted in the activity enhancement while preserving the inner pores of the inherent MOF.

Two-Phase System Utilizing Hydrophobic Metal-Organic Frameworks (MOFs) for Photocatalytic Synthesis of Hydrogen Peroxide.

Much effort has been devoted to photocatalytic production of hydrogen peroxide (H2 O2 ) as an alternative to fossil fuels. From an economic point of view, reductive synthesis of H2 O2 from O2 coupled with the oxidative synthesis of value-added products is particularly interesting. We herein report application of MIL-125-NH2 , a photoactive metal-organic framework (MOF), to a benzylalcohol/water two-phase system that realized photocatalytic production and spontaneous separation of H2 O2 and benzaldehyde. Hydrophobization of the MOF enabled its separation from the aqueous phase. This resulted in enhanced photocatalytic efficiency and enabled application of various aqueous solutions including extremely low pH solution which is favorable for H2 O2 production but fatal to MOF structure. In addition, a highly concentrated H2 O2 solution was obtained by simply reducing the volume of the aqueous phase.

Photocatalytic production of hydrogen peroxide through selective two-electron reduction of dioxygen utilizing amine-functionalized MIL-125 deposited with nickel oxide nanoparticles.

Photocatalytic H2O2 production via two-electron reduction of O2 was realized by visible-light irradiation of a metal-organic framework, MIL-125-NH2, in the presence of TEOA and benzylalcohol. Deposition of NiO nanoparticles onto MIL-125-NH2 dramatically enhanced the catalytic activity. Further studies suggested that fast disproportionation of the O2˙- intermediate to H2O2 resulted in the enhancement.