Laboratoire de Chimie et Biologie des Métaux , Université Grenoble Alpes , CNRS UMR 5249, CEA, 17 rue des Martyrs , F-38054 Grenoble Cedex, France.
Department of Chemistry, School of Science , Tokyo Institute of Technology , O-okayama 2-12-1-NE-1 , Meguro-ku , Tokyo 152-8550 , Japan.
J Am Chem Soc. 2019 Jun 19;141(24):9593-9602. doi: 10.1021/jacs.9b02521. Epub 2019 Jun 11.
A push-pull organic dye and a cobaloxime catalyst were successfully cografted on NiO and CuGaO to form efficient molecular photocathodes for H production with >80% Faradaic efficiency. CuGaO is emerging as a more effective p-type semiconductor in photoelectrochemical cells and yields a photocathode with 4-fold higher photocurrent densities and 400 mV more positive onset photocurrent potential compared to the one based on NiO. Such an optimized CuGaO photocathode was combined with a TaON|CoO photoanode in a photoelectrochemical cell. Operated in this Z-scheme configuration, the two photoelectrodes produced H and O from water with 87% and 88% Faradaic efficiency, respectively, at pH 7 under visible light and in the absence of an applied bias, equating to a solar to hydrogen conversion efficiency of 5.4 × 10%. This is, to the best of our knowledge, the highest efficiency reported so far for a molecular-based noble metal-free water splitting Z-scheme.
成功地将推挽有机染料和钴卟啉催化剂共接枝到 NiO 和 CuGaO 上,形成高效的分子光阴极,用于 H 生产,法拉第效率超过 80%。CuGaO 在光电化学电池中作为一种更有效的 p 型半导体出现,与基于 NiO 的光阴极相比,其光电流密度提高了 4 倍,起始光电流电位正移了 400 mV。将优化后的 CuGaO 光阴极与 TaON|CoO 光电阳极组合在光电化学电池中。在 Z 型结构中,在 pH 值为 7 下可见光照射和无外加偏压条件下,两个电极分别以 87%和 88%的法拉第效率从水中产生 H 和 O,相当于太阳能到氢气的转换效率为 5.4×10%。就我们所知,这是目前为止报道的最高效率的无贵金属分子基水分解 Z 型。