海水
电流密度
过电位
阴极
超亲水性
吸附
分解水
材料科学
化学工程
电解
无机化学
化学
催化作用
海洋学
电化学
物理
物理化学
电极
地质学
电解质
润湿
工程类
光催化
量子力学
生物化学
复合材料
作者
Jianpeng Sun,Zisheng Zhang,Xiangchao Meng
标识
DOI:10.1016/j.apcatb.2023.122703
摘要
Developing highly effective and stable electrocatalysts are attractive but highly challenging for alkaline seawater splitting. Herein, using a simple method, we developed a novel MOF derived nanosheets-nanoparticle-structured Pt2/Ni(OH)2/NF catalyst. Benefiting from strong metal-support interaction (SMSI) of Pt-O-Ni bond at interface, the synergistic effect of Pt-O vacancies (Ov) sites and excellent superhydrophilic surface, catalyst delivered excellent catalytic activity in seawater splitting. The overpotential was 19 mV at 10 mA·cm−2, which surpassed the commercial 20% Pt/C. A photovoltaic cell yielded up to 13.5% STH conversion efficiency. Furthermore, the cell voltage at 10 mA·cm−2 for anion exchange membrane (AEM) seawater electrolyzer in our design with the Pt2/Ni(OH)2/NF cathode catalyst was merely 1.46 V. The energy consumption to produce 1 m3 of H2 at the current density of 200 mA·cm−2 was 3.8 kW·h, below that of NF= |NF (4.3 kW·h). Theoretical results showed that the localized charge density and electronic structure of Ni(OH)2 can be significantly modulated upon SMSI at interface and Ov. And the synergistic effect of Pt-Ov sites can balance the adsorption and desorption of H* . Ov could achieve high-efficiency adsorption of H2O and optimize hydrogen spillover from Ni(OH)2 to Pt, leading to excellent HER activity. This study provided a light in rational construction of robust seawater-based electrocatalysts for seawater splitting.
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