Lai Yi-Hsuan, Park Hyun S, Zhang Jenny Z, Matthews Peter D, Wright Dominic S, Reisner Erwin
Christian Doppler Laboratory for Sustainable SynGas Chemistry, Department of Chemistry, University of Cambridge, Cambridge CB2 1EW (UK) http://www-reisner.ch.cam.ac.uk/
Chemistry. 2015 Mar 2;21(10):3919-23. doi: 10.1002/chem.201406566. Epub 2015 Feb 4.
An efficient, stable and scalable hybrid photoelectrode for visible-light-driven H2 generation in an aqueous pH 9.2 electrolyte solution is reported. The photocathode consists of a p-type Si substrate layered with a Ti and Ni-containing composite film, which acts as both a protection and electrocatalyst layer on the Si substrate. The film is prepared by the simple drop casting of the molecular single-source precursor, [{Ti2(OEt)9(NiCl)}2] (TiNipre), onto the p-Si surface at room temperature, followed by cathodic in situ activation to form the catalytically active TiNi film (TiNicat). The p-Si|TiNicat photocathode exhibits prolonged hydrogen generation with a stable photocurrent of approximately -5 mA cm(-2) at 0 V vs. RHE in an aqueous pH 9.2 borate solution for several hours, and serves as a benchmark non-noble photocathode for solar H2 evolution that operates efficiently under neutral-alkaline conditions.
报道了一种用于在pH值为9.2的水性电解质溶液中可见光驱动产氢的高效、稳定且可扩展的混合光电极。该光电阴极由p型硅衬底和含钛镍复合膜层组成,该复合膜层在硅衬底上既作为保护层又作为电催化剂层。该膜通过在室温下将分子单源前驱体[{Ti2(OEt)9(NiCl)}2](TiNipre)简单滴铸到p型硅表面,然后进行阴极原位活化以形成催化活性的TiNi膜(TiNicat)来制备。在pH值为9.2的硼酸盐水溶液中,相对于可逆氢电极(RHE)在0 V时,p-Si|TiNicat光电阴极在数小时内表现出持续产氢,光电流稳定在约-5 mA cm(-2),并作为在中性碱性条件下高效运行的太阳能制氢的基准非贵金属光电阴极。