电催化剂
析氧
材料科学
阳极
X射线光电子能谱
化学工程
微观结构
催化作用
双功能
电解质
纳米颗粒
分解水
纳米技术
电化学
电极
化学
复合材料
物理化学
有机化学
工程类
光催化
作者
Hongming Sun,Xiaobin Xu,Zhenhua Yan,Xiang Chen,Fangyi Cheng,Paul S. Weiss,Jun Chen
标识
DOI:10.1021/acs.chemmater.7b03627
摘要
Tailoring the morphology and microstructure of electrocatalysts is important in improving catalytic performance. Herein, porous multishelled Ni2P hollow microspheres assembled by nanoparticles were prepared through a simple and economical self-templating approach followed by phosphorization. Compared with nanoparticles and hierarchical solid-interior microspheres, the synthesized multishelled, hollow microstructures of Ni2P exhibit significantly higher electrocatalytic activity for the hydrogen evolution reaction in a 1 M KOH electrolyte. Additionally, a NiOOH layer is formed on the surface of Ni2P during anodic polarization, as revealed by electron microscopy, X-ray photoelectron spectroscopy, and in situ Raman analysis. The Ni2P/NiOOH derivative outperforms the benchmark RuO2 in catalyzing the oxygen evolution reaction. Furthermore, pairing the carbon fiber paper-supported multishelled Ni2P as both the anode and cathode results in superior overall alkaline water splitting performance, generating 10 and 20 mA cm–2 current densities at applied cell voltages of only 1.57 and 1.64 V, respectively, together with outstanding durability. These results suggest that further elaboration of the design of multishelled and hollow structured metal phosphides is desirable for application in hydrogen and oxygen evolution electrocatalysis.
科研通智能强力驱动
Strongly Powered by AbleSci AI