电催化剂
非阻塞I/O
分解水
析氧
双功能
材料科学
纳米颗粒
化学工程
X射线光电子能谱
计时安培法
纳米技术
无机化学
化学
催化作用
电化学
电极
循环伏安法
物理化学
光催化
生物化学
工程类
作者
Vishesh Manjunath,Santosh Bimli,Rathindranath Biswas,Pravin N. Didwal,Krishna Kanta Haldar,Mangesh Mahajan,Nishad G. Deshpande,P. A. Bhobe,Rupesh S. Devan
标识
DOI:10.1016/j.ijhydene.2022.09.054
摘要
Developing a single electrocatalyst effective for both oxygen and hydrogen evolution remains challenging. Although an attempt to utilize a single electrocatalyst for overall water splitting is made, there still exist several issues of efficiency and stability of the electrocatalyst. Hence, the present study reports on morphology-controlled NiO electrocatalyst, a single electrocatalyst for oxygen and hydrogen evolution. The cubic phase NiO nanoparticles and nanoplates of diameter and thickness <10 nm delivered surface-to-volume ratios of 0.078 and 0.083, respectively. XRD and TEM confirm the formation of NiO nanostructures, where morphology transformed independently of the chemical composition. XPS and EXAFS confirm the 2+ oxidation state of Ni ions and its octahedral coordination with oxygen. The 0D nanoparticles providing a larger surface area and active sites offered the overpotentials of 373 and 268 mV for OER and HER activity, respectively, and performed well than the 2D porous NiO nanoplates. The chronoamperometry and repetitive LSV cyclic studies confirmed the excellent long-term stability of 0D NiO nanoparticles in basic and acidic mediums during electrocatalytic water splitting reactions, owing to its increased electrochemically exposed active sites.
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