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Solar H2 generation in water with a CuCrO2 photocathode modified with an organic dye and molecular Ni catalyst

机译:用有机染料和分子镍催化剂修饰的CuCrO2光电阴极在水中产生太阳能H2

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摘要

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 CuCrO2 as a suitable p-type semiconductor for visible light-driven H2 generation upon co-immobilisation of a phosphonated diketopyrrolopyrrole dye with a Ni-bis(diphosphine) catalyst. The hybrid CuCrO2 photocathode displays an early photocurrent onset potential of +0.75 V vs. RHE and delivers a photocurrent of 15 μA cm–2 at 0.0 V vs. RHE in pH 3 aqueous electrolyte solution under UV-filtered simulated solar irradiation. Controlled potential photoelectrolysis at 0.0 V vs. RHE shows good stability and yields a Ni catalyst-based turnover number of 126 ± 13 towards H2 after 2 h. This precious metal-free system outperforms an analogous NiO|dye/catalyst assembly and therefore highlights the benefits of using CuCrO2 as a novel material for DSPEC applications.
机译:染料敏化光电化学(DSPEC)电池近年来已成为太阳能生产的一种途径。但是,燃料形成的阴极目前受到光腐蚀的窄带隙半导体或可用染料的低性能的小范围可用宽带隙p型半导体如NiO的限制。在这里,我们介绍了CuCrO2作为合适的p型半导体,用于将膦酸酯化的二酮吡咯并吡咯染料与Ni-双(二膦)催化剂共固定化后产生可见光驱动的H2。混合CuCrO2光电阴极在相对于RHE的情况下显示出+0.75 V的早期光电流起始电位,并且在pH相对于RHE的条件下,在pH 3的水溶液中,在经过UV过滤的情况下,提供的光电流为15μAcm –2 模拟太阳辐射。相对于RHE而言,在0.0 V的受控电位下进行光电解显示了良好的稳定性,并且在2 h后产生的基于Ni催化剂的H2转化数为126±13。这种不含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CuCrO2作为DSPEC应用的新型材料的好处。

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