Zhu Kaijian, Mul Guido, Huijser Annemarie
PhotoCatalytic Synthesis Group, MESA+ Institute for Nanotechnology, University of Twente, P.O. Box 217, 7500 AE, Enschede (The, Netherlands.
ChemSusChem. 2024 Jan 22;17(2):e202300800. doi: 10.1002/cssc.202300800. Epub 2023 Nov 3.
P-type metal oxides, and in particular NiO, are typically used as hole accepting layers in dye-sensitized photocathodes. Delafossites (CuMO ) with M=B, Al, Cr or Ga have recently been proposed as attractive substitutes for NiO, with theoretically a higher hole mobility than NiO, therefore allowing a higher efficiency when the photocathode is applied in solar to fuel devices. We have experimentally validated the photoelectrochemical performance of photocathodes consisting of nanoporous CuBO (CBO) on Fluorine-doped Tin Oxide substrates, photosensitized with a light absorbing P1 dye. Femtosecond transient absorption and time-resolved photoluminescence studies show that light-induced hole injection occurs from the P1 dye into the CBO in a few ps, comparable to the time constant observed for NiO-based photocathodes. Importantly, the CBO-based photocathode shows significantly slower charge recombination than the NiO-based analogue. These results illustrate the promise of CBO as a p-type semiconductor in solar energy conversion devices.
P型金属氧化物,尤其是氧化镍(NiO),通常用作染料敏化光阴极中的空穴接受层。最近有人提出,M为B、Al、Cr或Ga的铜铁矿(CuMO)可作为氧化镍的理想替代品,理论上空穴迁移率比氧化镍更高,因此当光阴极应用于太阳能制燃料装置时效率更高。我们通过实验验证了由氟掺杂氧化锡衬底上的纳米多孔CuBO(CBO)组成的光阴极的光电化学性能,该光阴极用吸光P1染料进行了光敏化处理。飞秒瞬态吸收和时间分辨光致发光研究表明,光诱导空穴在几皮秒内从P1染料注入到CBO中,这与基于氧化镍的光阴极观察到的时间常数相当。重要的是,基于CBO的光阴极显示出比基于氧化镍的类似物明显更慢的电荷复合。这些结果说明了CBO作为太阳能转换装置中p型半导体的前景。