Anomalous Enhancement of the Electrocatalytic Hydrogen Evolution Reaction in AuPt Nanoclusters

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL
Jiahui Kang, Jan Kloppenburg, Jiali Sheng, Zhenyu Xu, Kristoffer Meinander, Hua Jiang, Zhong-Peng Lv, Esko I. Kauppinen, Qiang Zhang, Xi Chen, Milla Vikberg, Olli Ikkala, Miguel A. Caro, Bo Peng
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Abstract

Energy- and resource-efficient electrocatalytic water splitting is of paramount importance to enable hydrogen production. The best bulk catalyst for the hydrogen evolution reaction (HER), platinum, is one of the scarcest elements on Earth. The use of nanoclusters significantly reduces the amount of raw material required for HER, while nanoalloying further enhances performance by modulating hydrogen adsorption. However, the interplay between the atomic structure and HER performance in alloyed nanoclusters remains unclear. In this study, we report an anomalous HER enhancement at low and intermediate Au contents in monodisperse AuPt nanoclusters immobilized on carbon nanotubes. This enhancement is driven by the segregation of Au atoms toward the nanocluster surface and a synergistic effect, whereby the ability of surface Pt atoms to bind hydrogen is increased in the presence of adjacent Au atoms. This enhancement is noteworthy and “anomalous”, given that the overall hydrogen adsorption activity significantly decreases for pure Au nanoclusters compared to pure Pt nanoclusters. We rationalize these observations by combining extensive experimental characterization data with detailed atomistic simulations based on purpose-built machine learning interatomic potential and Markov-chain Monte Carlo simulations with variable chemical potential. The agreement between simulation and experiment allows us to develop a mechanistic understanding of the atomic-scale processes underlying the enhanced HER activity.

Abstract Image

AuPt纳米团簇中电催化析氢反应的异常增强
能源和资源节约型电催化水分解对于实现氢气生产至关重要。铂是析氢反应(HER)的最佳体催化剂,是地球上最稀缺的元素之一。纳米团簇的使用大大减少了HER所需的原材料数量,而纳米合金化通过调节氢吸附进一步提高了性能。然而,在合金纳米团簇中,原子结构与she性能之间的相互作用尚不清楚。在这项研究中,我们报道了固定在碳纳米管上的单分散AuPt纳米簇在低和中等Au含量时的异常HER增强。这种增强是由Au原子向纳米团簇表面的偏析和协同效应驱动的,即在相邻Au原子存在的情况下,表面Pt原子结合氢的能力增加。考虑到与纯铂纳米团簇相比,纯金纳米团簇的整体氢吸附活性显著降低,这种增强是值得注意的,也是“反常的”。我们通过将广泛的实验表征数据与基于专用机器学习原子间势的详细原子模拟和具有可变化学势的马尔可夫链蒙特卡罗模拟相结合,使这些观察结果变得合理。模拟和实验之间的一致性使我们能够对增强的HER活动背后的原子尺度过程进行机械理解。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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