College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China.
Department of Chemical and Materials Engineering, Gina Cody School of Engineering and Computer Science, Concordia University, Montreal QC H3G 2W1, Canada.
Sci Adv. 2023 Jan 4;9(1):eade4589. doi: 10.1126/sciadv.ade4589.
Photoelectrochemical (PEC) water splitting that functions in pH-neutral electrolyte attracts increasing attention to energy demand sustainability. Here, we propose a strategy to in situ form a NiB layer by tuning the composition of the neutral electrolyte with the additions of nickel and borate species, which improves the PEC performance of the BiVO photoanode. The NiB/BiVO exhibits a photocurrent density of 6.0 mA cm at 1.23 V with an onset potential of 0.2 V under 1 sun illumination. The photoanode displays a photostability of over 600 hours in a neutral electrolyte. The additive of Ni in the electrolyte, which efficiently inhibits the dissolution of NiB, can accelerate the photogenerated charge transfer and enhance the water oxidation kinetics. The borate species with B─O bonds act as a promoter of catalyst activity by accelerating proton-coupled electron transfer. The synergy effect of both species suppresses the surface charge recombination and inhibits the photocorrosion of BiVO.
光电化学(PEC)水分解在中性电解质中进行,能满足能源需求的可持续性,因此受到越来越多的关注。在这里,我们提出了一种通过调节中性电解质的组成,原位形成 NiB 层的策略,从而提高 BiVO 光阳极的 PEC 性能。NiB/BiVO 在 1 个太阳光照下,起始电位为 0.2 V 时,其光电流密度为 6.0 mA cm。在中性电解质中,光阳极具有超过 600 小时的光稳定性。电解质中 Ni 的添加可以有效地抑制 NiB 的溶解,从而加速光生载流子的转移并增强水氧化动力学。具有 B─O 键的硼酸盐通过促进质子耦合电子转移,作为催化剂活性的促进剂。两种物质的协同效应抑制了表面电荷复合并抑制了 BiVO 的光腐蚀。