尼亚尔
过电位
电催化剂
双功能
析氧
分解水
塔菲尔方程
材料科学
催化作用
无机化学
化学工程
电化学
化学
电极
冶金
物理化学
合金
金属间化合物
有机化学
工程类
光催化
作者
Rajathsing Kalusulingam,Mariyamuthu Mariyaselvakumar,Churchil A. Antonyraj,Selvam Mathi,Tatiana S. Mikhailova,Soslan A. Khubezhov,Ilya Pankov,Kannan Srinivasan,Tatiana N. Myasoedova
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2023-08-22
卷期号:37 (17): 13319-13330
被引量:35
标识
DOI:10.1021/acs.energyfuels.3c02213
摘要
Electrochemical water splitting is one among multiple ways toward attaining clean energy systems, which demand efficient bifunctional catalysts. In this study, we report the synthesis of Pd-embedded NiAl-layered double hydroxide (LDH) nanosheets by a well-known coprecipitation technique, which showed superior performance in this reaction due to highly dispersed Pd in the sheets. Enhanced catalytic performance was achieved for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) using as-prepared Pd-NiAl-LDH nanosheets in a 1.0 M KOH solution. The Pd-NiAl-LDH materials exhibited substantially improved activity, stability, and overpotential, with the Tafel value for OER being 264 mV (99.5 mV/dec) and HER being 189 mV (133.2 mV/dec) at 10 mA/cm2. Pd-NiAl-LDH electrocatalyst remained stable for 48 h with minimal potential deviations observed in both OER and HER. Moreover, Pd-NiAl-LDH materials showed better activity than NiAl-LDH. With the active bifunctional Pd-NiAl-LDH electrode pair, we successfully fabricated a water electrolyzer achieving a current density of 10 mA/cm2 at a cell voltage of 1.59 V. The Pd-NiAl-LDH //Pd-NiAl-LDH configuration showed good stability over 48 h with a minimal potential deviation during the overall water splitting. Continuous generation of hydrogen and oxygen is conceivable in the solar cell configuration using the active bifunctional Pd-NiAl-LDH electrocatalyst, enabling hydrogen production in a large scale with a cell voltage of 1.60 V.
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