塔菲尔方程
电催化剂
过电位
镍
X射线光电子能谱
铂金
材料科学
催化作用
电化学
分解水
化学工程
化学
无机化学
冶金
电极
物理化学
光催化
工程类
生物化学
作者
Elif Demir Arabacı,Ahmet M. Önal,Saim Özkâr
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2020-06-17
卷期号:167 (10): 106513-106513
被引量:9
标识
DOI:10.1149/1945-7111/ab9d93
摘要
Herein, we report the development of a nickel-based catalyst obtained by reduction of Ni2+ ions on the surface of ceria nanopowder using aqueous solution of NaBH4. The catalyst was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX) and X-ray photoelectron spectroscopy (XPS). Nickel(0) nanoparticles supported on nanoceria (Ni0/CeO2) were employed as electrocatalyst on glassy carbon electrode (GCE) for H2 evolution reaction. The modified Ni0/CeO2-GCE requires a relatively small overpotentials of 150 mV, 175 mV and 203 mV to drive current densities of 10, 20 and 50 mA cm−2, respectively. Tafel slope, 80 mV dec−1, indicates that HER process follows the Volmer-Heyrovsky mechanism with relatively high turnover frequency (TOF), i.e. 0.41 and 5.84 s−1 at an overpotential of 100 and 200 mV, respectively. A drastic enhancement in the electrocatalytic activity of Ni0/CeO2-GCE was observed when platinum wire was used as counter electrode instead of graphite rod, especially after long term potential cycling due to platinum dissolution and deposition on the modified electrode. Ni0/CeO2-GCE was found to exhibit high electrochemical stability (i.e. a small change both in the Tafel slope and onset potential) after 2000 CV scans in 0.5 M H2SO4, which makes Ni0/CeO2 a potential electrocatalyst for H2 evolution from water.
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