过电位
分解水
无定形固体
电催化剂
材料科学
异质结
析氧
化学工程
双功能
兴奋剂
催化作用
过渡金属
纳米技术
化学
物理化学
电极
光电子学
结晶学
电化学
光催化
生物化学
工程类
作者
Jiaxin Li,Yan Lv,Xueyan Wu,Kenan Zhao,Jixi Guo,Binhai He,Dianzeng Jia
标识
DOI:10.1016/j.jcis.2023.07.070
摘要
It is very important to develop transition metal-based electrocatalysts with excellent activity, high stability and low-cost for overall water splitting. In this work, the Fe-doped NixSy/NF amorphous/crystalline heterostructure nanoarrays (Fe-NixSy/NF) was synthesized by a simple one-step method. The resulting hierarchically structured nanoarrays offer the advantages of large surface area, high structural void fraction and accessible internal surfaces. These advantages not only furnish additional catalytically active sites, but also enhance the stability of the structure and effectively accelerate mass diffusion and charge transport. Experimental and characterization results indicate that Fe doping increases the electrical conductivity of amorphous/crystalline NixSy/NF, and the NiS-Ni3S2 heterojunctions evoke interfacial charge rearrangement and optimize the adsorption free energy of the intermediates, which allows the catalyst to exhibit low overpotential and superior electrocatalytic activity. Especially, the overpotentials of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) of Fe-NixSy/NF at 10 mA cm-2 in an alkaline environment are 102.4 and 230.5 mV, respectively. When applied as a bifunctional catalyst for overall water splitting, it requires only 1.45 V cell voltage to deliver a current density of 10 mA cm-2, which is preferable to the all-noble metal Pt/C || IrO2 electrocatalyst (1.62 mV @ 10 mA cm-2). In addition, Fe-NixSy/NF has excellent stability, and there is no obvious degradation after 96 h continuous operation at a current density of 100 mA cm-2. This work affords insights into the application of doping strategies and crystalline/amorphous synergistic modulation of the electrocatalytic activity of transition metal-based catalysts in energy conversion systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI