Chen Hongjun, Bo Renheng, Tran-Phu Thanh, Liu Guanyu, Tricoli Antonio
Nanotechnology Research Laboratory, Research School of Engineering, Australian National University, Canberra, ACT, 2601, Australia.
CSIRO, Black Mountain, Canberra, ACT, 2601, Australia.
Chempluschem. 2018 Jul;83(7):569-576. doi: 10.1002/cplu.201800061. Epub 2018 Apr 16.
Photoelectrochemical water splitting is a promising approach for the carbon-free production of hydrogen using sunlight. Here, robust and efficient WO photoanodes for water oxidation were synthesized by the scalable one-step flame synthesis of nanoparticle aerosols and direct gas-phase deposition. Nanostructured WO films with tunable thickness and band gap and controllable porosity were fabricated by controlling the aerosol deposition time, concentration, and temperature. Optimal WO films demonstrate superior water oxidation performance, reaching a current density of 0.91 mA at 1.24 V vs. reversible hydrogen electrode (RHE) and an incident photon-to-current conversion efficiency (IPCE) of ca. 61 % at 360 nm in 0.1 m H SO . Notably, it is found that the excellent performance of these WO nanostructures arises from the high in situ restructuring temperature (ca. 1000 °C), which increases oxygen vacancies and decreases charge recombination at the WO /electrolyte interface. These findings provide a scalable approach for the fabrication of efficient photoelectrodes based on WO and other metal oxides for light-driven water splitting.
光电化学水分解是一种利用阳光进行无碳制氢的很有前景的方法。在此,通过纳米颗粒气溶胶的可扩展一步火焰合成法和直接气相沉积法合成了用于水氧化的坚固且高效的WO光阳极。通过控制气溶胶沉积时间、浓度和温度,制备了具有可调厚度、带隙和可控孔隙率的纳米结构WO薄膜。优化后的WO薄膜表现出优异的水氧化性能,在相对于可逆氢电极(RHE)为1.24 V时,电流密度达到0.91 mA,在0.1 m H₂SO₄中360 nm处的入射光子到电流转换效率(IPCE)约为61%。值得注意的是,发现这些WO纳米结构的优异性能源于较高的原位重构温度(约1000 °C),这增加了氧空位并减少了WO₃/电解质界面处的电荷复合。这些发现为基于WO₃和其他金属氧化物制造用于光驱动水分解的高效光电极提供了一种可扩展的方法。