多金属氧酸盐
过电位
析氧
电解
异质结
分解水
电解水
电催化剂
密度泛函理论
电流密度
化学工程
化学
材料科学
交换电流密度
可再生能源
电极
纳米技术
电化学
光电子学
光催化
计算化学
催化作用
电气工程
工程类
物理化学
塔菲尔方程
物理
生物化学
电解质
量子力学
作者
Yukun Lu,Xinxin Guo,Lingyu Yang,Wei Yang,Wanting Sun,Yongxiao Tuo,Yan Zhou,Shutao Wang,Yuan Pan,Wenfu Yan,Daofeng Sun,Yunqi Liu
标识
DOI:10.1016/j.cej.2020.124849
摘要
Electrocatalytic overall water splitting is always holding great promise in renewable energy field. It is crucial to fabricate low-cost, earth-abundant and robust bi-functional electrocatalysts for both hydrogen evolution and oxygen evolution reactions. Herein, we report a polyoxometalates (POMs)-based molecular approach to construct Co promoting MoS2-based nanosheets Co5Mo10Sx employing well-defined Co3[Co2Mo10O38H4] as superior precursor. The CoMo-POMs act as pre-assembling molecular platform for the construction and regulation of CoS2-MoS2 heteronanostructure (CoMoS active sites) through precise engineering with atomic level. The Co5Mo10Sx exhibited excellent bi-functional electrocatalytic activity in alkaline solution, with only 36 mV and 153 mV overpotential to achieve 10 mA cm−2 current density for HER and OER, respectively. We demonstrate a two-electrode cell performing water electrolysis in alkaline condition, delivering a current density of 10 mA cm−2 at low cell voltage of 1.51 V. Combined with the theoretical calculations, the superior performance can be attributed to enhanced intrinsic catalytic activity of CoMoS sites, synergistic effect of heterostructure, abundant and defect-rich heterogeneous interfaces. This study provides a feasible strategy to rational design and controllable fabrication of efficient electrocatalysts for renewable energy applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI