Miao Fang, Cui Peng, Gu Tao, Yu Shijie, Yan Zhijie, Hai Guangtong
College of Materials Science and Engineering, North University of China, Taiyuan 030051, China.
Shanxi Key Laboratory of Advanced Metal Materials for Special Environments, North University of China, Taiyuan 030051, China.
Dalton Trans. 2024 Jan 23;53(4):1599-1606. doi: 10.1039/d3dt02804f.
The rational modification of electronic structures to create catalytically active sites has been proved to be a promising strategy to efficiently facilitate the urea oxidation reaction (UOR). Herein, a well-defined nanosheet arrays catalyst of Ni(OH) doped with dual cations of Co and Mn on Ni foam (NF) (Co/Mn-Ni(OH)) is synthesized through a simple hydrothermal process. Benefiting from the advantages of unique structures and modified binding strengths, it is found experimentally that the obtained Co/Mn-Ni(OH) catalyst only requires a potential of 1.38 V to deliver a current density of 100 mA cm and exhibits a small Tafel slope of 35 mV dec, outperforming single-component-incorporated Ni(OH). Moreover, the catalyst has shown excellent stability for 25 h at a current density of 50 mA cm. Additionally, first-principles calculations demonstrate that the co-incorporation of Co and Mn remarkably lowers the adsorption barrier of CO(NH)* on the catalyst surface, and accelerates the dissociation of the CO(NH)* intermediate into CO* and NH* intermediates, which synergistically improve the UOR reaction kinetics. This work provides a generic paradigm for designing advanced and effective catalysts toward the UOR.
通过合理修饰电子结构来创建催化活性位点已被证明是一种有效促进尿素氧化反应(UOR)的有前景的策略。在此,通过简单的水热过程合成了一种在泡沫镍(NF)上掺杂有Co和Mn双阳离子的Ni(OH)纳米片阵列催化剂(Co/Mn-Ni(OH))。得益于独特结构和修饰后的结合强度的优势,实验发现所制备的Co/Mn-Ni(OH)催化剂仅需1.38 V的过电位就能实现100 mA cm的电流密度,并且具有35 mV dec的小塔菲尔斜率,优于单组分掺杂的Ni(OH)。此外,该催化剂在50 mA cm的电流密度下表现出25 h的优异稳定性。另外,第一性原理计算表明,Co和Mn的共掺杂显著降低了CO(NH)在催化剂表面的吸附能垒,并加速了CO(NH)中间体分解为CO和NH中间体,协同改善了UOR反应动力学。这项工作为设计用于UOR的先进高效催化剂提供了一种通用范例。