Creissen Charles E, Warnan Julien, Reisner Erwin
Christian Doppler Laboratory for Sustainable SynGas Chemistry , Department of Chemistry , Lensfield Road , Cambridge CB2 1EW , UK . Email:
Chem Sci. 2017 Nov 27;9(6):1439-1447. doi: 10.1039/c7sc04476c. eCollection 2018 Feb 14.
Dye-sensitised photoelectrochemical (DSPEC) cells have emerged in recent years as a route to solar fuel production. However, fuel-forming photocathodes are presently limited by photo-corrodible narrow band gap semiconductors or the small range of available wide bandgap p-type semiconductors such as NiO that display low performance with dyes. Here, we introduce CuCrO as a suitable p-type semiconductor for visible light-driven H generation upon co-immobilisation of a phosphonated diketopyrrolopyrrole dye with a Ni-bis(diphosphine) catalyst. The hybrid CuCrO photocathode displays an early photocurrent onset potential of +0.75 V RHE and delivers a photocurrent of 15 μA cm at 0.0 V RHE in pH 3 aqueous electrolyte solution under UV-filtered simulated solar irradiation. Controlled potential photoelectrolysis at 0.0 V RHE shows good stability and yields a Ni catalyst-based turnover number of 126 ± 13 towards H after 2 h. This precious metal-free system outperforms an analogous NiO|dye/catalyst assembly and therefore highlights the benefits of using CuCrO as a novel material for DSPEC applications.
近年来,染料敏化光电化学(DSPEC)电池已成为一种生产太阳能燃料的途径。然而,目前用于燃料生成的光阴极受到光腐蚀窄带隙半导体的限制,或者受到可用的宽带隙p型半导体范围较小的限制,例如与染料结合时表现出低性能的NiO。在此,我们引入CuCrO作为一种合适的p型半导体,用于在将膦酸化二酮吡咯并吡咯染料与镍双(二膦)催化剂共固定时实现可见光驱动的氢气生成。在经过紫外线过滤的模拟太阳辐射下,混合的CuCrO光阴极在pH 3的水性电解质溶液中显示出+0.75 V(相对于可逆氢电极)的早期光电流起始电位,并在0.0 V(相对于可逆氢电极)时提供15 μA/cm²的光电流。在0.0 V(相对于可逆氢电极)下进行的控制电位光电电解显示出良好的稳定性,并在2小时后产生基于镍催化剂的氢气周转数为126 ± 13。这个无贵金属的系统优于类似的NiO|染料/催化剂组件,因此突出了使用CuCrO作为DSPEC应用新型材料的优势。