Devi Aarti, Minhas Harpriya, Sahoo Lipipuspa, Gratious Saniya, Das Amitabha, Mandal Sukhendu, Pathak Biswarup, Patra Amitava
Institute of Nano Science and Technology, Knowledge City, Sector 81, Mohali 14036, India.
Department of Chemistry, Indian Institute of Technology (IIT) Indore, Indore, Madhya Pradesh, 453552, India.
Nanoscale. 2024 Jan 25;16(4):1758-1769. doi: 10.1039/d3nr05445d.
The design of efficient electrocatalysts for improving hydrogen evolution reaction (HER) performance using atomically precise metal nanoclusters (NCs) is an emerging area of research. Here, we have studied the HER electrocatalytic performance of monometallic Cu and Au nanoclusters and bimetallic AuCu nanoclusters. A bimetallic AuCu/MoS composite exhibits excellent HER catalytic activity with an overpotential () of 155 mV reversible hydrogen electrode observed at 10 mA cm current density. The improved HER performance in AuCu is due to the increased electrochemically active surface area (ECSA), and AuCu NCs exhibits better stability than Cu and Au systems and bare MoS. This augmentation offers a greater number of active sites for the favorable adsorption of reaction intermediates. Furthermore, by employing X-ray photoelectron spectroscopy (XPS) and Raman analysis, the kinetics of HER in the AuCu/MoS composite were elucidated, attributing the favorable performance to better electronic interactions occurring at the interface between AuCu NCs and the MoS substrate. Theoretical analysis reveals that the inherent catalytic enhancement in AuCu/MoS is due to favorable H atom adsorption over it and the smallest Δ value. The downshift in the d-band of the AuCu/MoS composite influences the binding energy of intermediate catalytic species. This new catalyst sheds light on the structure-property relationship for improving electrocatalytic performance at the atomic level.
利用原子精确的金属纳米团簇(NCs)设计高效的电催化剂以提高析氢反应(HER)性能是一个新兴的研究领域。在此,我们研究了单金属铜和金纳米团簇以及双金属金铜纳米团簇的HER电催化性能。一种双金属AuCu/MoS复合材料在10 mA cm电流密度下表现出优异的HER催化活性,观察到的过电位()为155 mV(可逆氢电极)。AuCu中HER性能的改善归因于电化学活性表面积(ECSA)的增加,并且AuCu NCs比铜和金体系以及裸MoS表现出更好的稳定性。这种增强为反应中间体的有利吸附提供了更多的活性位点。此外,通过采用X射线光电子能谱(XPS)和拉曼分析,阐明了AuCu/MoS复合材料中HER的动力学,将良好的性能归因于AuCu NCs与MoS基底之间界面处发生的更好的电子相互作用。理论分析表明,AuCu/MoS中固有的催化增强归因于其上有利的H原子吸附和最小的Δ值。AuCu/MoS复合材料d带的下移影响了中间催化物种的结合能。这种新型催化剂为在原子水平上改善电催化性能的结构-性能关系提供了启示。