In situ construction of hybrid Co(OH)2 nanowires for promoting long-term water splitting

塔菲尔方程 过电位 X射线光电子能谱 催化作用 分解水 纳米线 材料科学 化学工程 电解质 电子转移 纳米技术 化学 电极 光化学 光催化 电化学 物理化学 工程类 生物化学
作者
Shujie Liu,Rui‐Ting Gao,Mao Sun,Yan Wang,Tomohiko Nakajima,Xianhu Liu,Wei Zhang,Lei Wang
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:292: 120063-120063 被引量:77
标识
DOI:10.1016/j.apcatb.2021.120063
摘要

Engineering the interfacial structure of hybrid catalysts is crucial for enhanced electrocatalytic performances. Herein, a new strongly heterogeneous catalyst of Co/CoO/Co(OH)2 nanowires with proper interfacial structure was synthesized via a plasma etching approach. X-ray photoelectron spectroscopy and electron energy loss spectroscopy revealed that strong chemical couplings at the hybrid interface induced fast charge transfer, leading to considerable amounts of Co2+/Co sites present in the hybrid. The high conductivity from metal Co and one dimensional nanostructure favored the electron transfer and electrolyte access. The metallic Co was further oxidized to Co2+/Co3+ to address instability under applied potential during long-term testing. The resulting catalyst exhibited an excellent overpotential of 266 mV at 20 mA cm−2 and a Tafel slope of 85 mV dec−1 in alkaline medium. Importantly, the hybrid Co/CoO/Co(OH)2 demonstrated a super long-term durability over 200 h among the most ultra-long stability Co-based OEC catalysts. This catalyst was applied on light absorbing BiVO4 for solar-driven water splitting, exhibiting a significantly enhanced photoelectrochemical (PEC) activity, 5.32 mA cm−2 obtained at 1.23 VRHE, which represented one of the best performances achieved by Co-based OER cocatalysts.
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