Enhanced Photoelectrochemical Water Splitting of Black Silicon Photoanode with pH‐Dependent Copper‐Bipyridine Catalysts
Jing‐Xin Jian, Jia‐Xin Liao, Mu‐Han Zhou, Mingming Yao, Yijing Chen, Xi‐Wen Liang, Chao Ping Liu, Qing‐Xiao Tong
Abstract
Abstract Since the water oxidation half‐reaction requires the transfer of multi‐electrons and the formation of O−O bond, it's crucial to investigate the catalytic behaviours of semiconductor photoanodes. In this work, a bio‐inspired copper‐bipyridine catalyst of Cu(dcbpy) is decorated on the nanoporous Si photoanode (black Si, b ‐Si). Under AM1.5G illumination, the b ‐Si/Cu(dcbpy) photoanode exhibits a high photocurrent density of 6.31 mA cm −2 at 1.5 V RHE at pH 11.0, which is dramatically improved from the b ‐Si photoanode (1.03 mA cm −2 ) and f ‐Si photoanode (0.0087 mA cm −2 ). Mechanism studies demonstrate that b ‐Si/Cu(dcbpy) has improved light‐harvesting, interfacial charge‐transfer, and surface area for water splitting. More interestingly, b ‐Si/Cu(dcbpy) exhibits a pH‐dependent water oxidation behaviour with a minimum Tafel slope of 241 mV/dec and the lowest overpotential of 0.19 V at pH 11.0, which is due to the monomer/dimer equilibrium of copper catalyst. At pH ∼11, the formation of dimeric hydroxyl‐complex could form O−O bond through a redox isomerization (RI) mechanism, which decreases the required potential for water oxidation. This in‐depth understanding of pH‐dependent water oxidation catalyst brings insights into the design of dimer water oxidation catalysts and efficient photoanodes for solar energy conversion.