过电位
电催化剂
析氧
化学工程
催化作用
纳米技术
电流密度
制氢
材料科学
分解水
无机化学
交换电流密度
氢
化学
电极
电化学
物理化学
塔菲尔方程
有机化学
工程类
光催化
物理
量子力学
作者
Zhixin Dai,Xiaoqiang Du,Xiaoshuang Zhang
标识
DOI:10.1016/j.jallcom.2023.169451
摘要
The development of efficient, stable and low-cost electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is the key to promote the industrialization of electrocatalytic water splitting. In this paper, the CoFe-LDH@NiCo-LDH precursor was first synthesized and then the target catalyst named Ni-Co-Fe-Se@NiCo-LDH was finally synthesized by a selenization reaction based on this precursor. In a three-electrode system with 1.0 M KOH alkaline atmosphere, Ni-Co-Fe-Se@NiCo-LDH requires an overpotential of 286 mV to deliver a current density of 100 mA/cm2 for OER and 113 mV at a current density of 10 mA/cm2 for HER. In addition, the material shows excellent overall water splitting performance and a low cell voltage of 1.55 V at 10 mA/cm2 is expected. By comparing the test results of CoFe-LDH@NiCo-LDH and NiCo-LDH, we found that increasing the number of metal species only slightly reduces the electron transfer impedance and does not help to increase the electrochemical surface area of the material. Density functional theory calculation shows that the presence of the Co-NiSe2 material accelerates the kinetics of hydrogen production and the Fe7Se8 material enhances the conductivity of the material. Their synergistic effect makes the Ni-Co-Fe-Se@NiCo-LDH catalyst exhibit enhanced hydrogen production activity.
科研通智能强力驱动
Strongly Powered by AbleSci AI