过电位
材料科学
电催化剂
析氧
层状双氢氧化物
双功能
分解水
化学工程
异质结
电解
电极
无机化学
催化作用
电化学
光电子学
物理化学
氢氧化物
光催化
化学
电解质
工程类
生物化学
作者
Yun Li,Hao Xu,Peixia Yang,Ruopeng Li,Dan Wang,Penghui Ren,Shanshan Ji,Xiangyu Lu,Fan Meng,Jinqiu Zhang,Maozhong An
标识
DOI:10.1016/j.mtener.2022.100975
摘要
Reasonably constructing heterostructure is an efficient strategy to improve the intrinsic activity of catalyst for both hydrogen and oxygen evolution reactions. Herein, a heterostructure of CoNiP and NiFe layered double hydroxides (CoNiP@NiFe LDHs) is successfully prepared via a quick two-step electrodeposition method. The electrons rearrangement at the interface composed of CoNiP and NiFe LDHs promoted by the disparity of their unique work functions can increase the electron density of CoNiP, further optimizing the Gibbs free energy for the adsorption of hydrogen. Thus, CoNiP@NiFe LDHs need a low overpotential of 68 mV to reach 10 mA cm −2 . Meanwhile, the modulated valence band energy level ( E VB ) and holes collection at the space charge region of NiFe LDHs layer significantly enhance the oxygen evolution reaction performance of CoNiP@NiFe LDHs, which presents a low overpotential of 255 mV at 50 mA cm −2 . The assembled electrolyzer using CoNiP@NiFe LDHs as electrodes also exhibits a low cell voltage of 1.59 V at 50 mA cm −2 . • A janus CoNiP@NiFe layered double hydroxides heterostructure electrocatalyst was prepared by two-step electrodeposition method. • A low cell voltage of 1.59 V at 50 mA cm −2 was obtained by the assembled two-electrode electrolyzer. • The electronic coupling at the interface induces the enhanced hydrogen evolution reaction and oxygen evolution reaction performance.
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