过电位
制氢
电解
高压电解
析氧
电催化剂
阳极
电解水
高温电解
电解槽
氢
聚合物电解质膜电解
分解水
联氨(抗抑郁剂)
化学
光伏系统
材料科学
无机化学
化学工程
电解质
电极
催化作用
电化学
有机化学
电气工程
物理化学
工程类
光催化
色谱法
作者
Xin Xiao,Shuangshuang Liu,Dekang Huang,Xiaowei Lv,Man Li,Xingxing Jiang,Leiming Tao,Zehui Yu,Yong Shao,Mingkui Wang,Yan Shen
出处
期刊:Chemsuschem
[Wiley]
日期:2018-12-06
卷期号:12 (2): 434-440
被引量:16
标识
DOI:10.1002/cssc.201802512
摘要
Abstract Efficient hydrogen production by a photovoltaic‐electrolysis cell (PV–EC) system requires a low electrolyzer overpotential and a high coupling efficiency between both the components. Herein, Ni 5 P 4 is proposed as a cost‐effective bifunctional electrocatalyst for hydrogen evolution and hydrazine oxidation in a reformed electrolyzer. Experiments indicate that the electrolytic overpotential could be significantly reduced by replacing the oxygen evolution reaction with the hydrazine oxidation reaction at the anode. Furthermore, a scenario for hydrogen production is demonstrated by utilizing a stable and low‐cost perovskite solar cell (PSC) with a carbon back electrode to drive a reformed electrolyzer. Importantly, a single PSC can drive three reformed electrolyzers in series for hydrogen production by carefully matching the operating point of the electrolyzer with the maximum power point of the photovoltaic device, thereby, yielding a H 2 evolution rate of 1.77 mg h −1 for the whole PV–EC system. This can be a potential starting point for hydrogen production using a single PSC‐driven electrolysis system.
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