Lim Sung Yul, Seo Daye, Jang Min Seok, Chung Taek Dong
Department of Chemistry and Research Institute for Basic Science, Kyung Hee University, Seoul 02447, Korea.
Department of Chemistry, Seoul National University, Seoul 08826, Korea.
ACS Omega. 2021 Aug 22;6(34):22311-22316. doi: 10.1021/acsomega.1c03014. eCollection 2021 Aug 31.
Low-cost catalysts with high activity and durability are necessary to achieve efficient large-scale energy conversion in photoelectrochemical cell (PEC) systems. An additional factor that governs the construction of photoelectrodes for PECs is the spatial control of the catalysts for efficient utilization of photogenerated charge carriers. Here, we demonstrate spatial decoupling of the light-absorbing and catalytic components in hierarchically structured Si-based photocathodes for the hydrogen evolution reaction (HER). By simply modifying a well-known metal-assisted chemical etching procedure, we fabricated a Si nanowire (NW) array-based photocathode with Ag-Pt catalysts at the base and small amounts of the Pt catalyst at the NW tips. This approach simultaneously mitigates the parasitic light absorption by the catalytic layers and recombination of charge carriers owing to the long transport distance, resulting in improved photoelectrochemical HER performance under simulated AM 1.5G illumination.
低成本且具有高活性和耐久性的催化剂对于在光电化学电池(PEC)系统中实现高效大规模能量转换是必不可少的。影响PEC光电极构建的另一个因素是催化剂的空间控制,以便有效利用光生电荷载流子。在此,我们展示了用于析氢反应(HER)的分级结构硅基光阴极中光吸收和催化组分的空间解耦。通过简单修改一种广为人知的金属辅助化学蚀刻工艺,我们制备了一种基于硅纳米线(NW)阵列的光阴极,其底部有Ag-Pt催化剂,NW尖端有少量Pt催化剂。这种方法同时减轻了催化层的寄生光吸收以及由于长传输距离导致的电荷载流子复合,从而在模拟AM 1.5G光照下提高了光电化学HER性能。