Copper-based molecular complexes: next-Gen electrocatalysts for the green hydrogen evolution reaction

IF 4.6 3区 材料科学 Q2 CHEMISTRY, PHYSICAL
Sumana Roy, Dilip Sarkar, Jit Satra and Rajesh Kumar Das
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Abstract

Electrochemical water splitting is a key technology for sustainable green hydrogen (H2) production, yet its large-scale operation demands earth-abundant and cost-effective electrocatalysts capable of functioning efficiently with sufficiently low overpotentials with significant durability. In this scenario, copper-based molecular complexes are emerging catalysts which show promising results in the field of electrocatalytic green hydrogen evolution reaction (HER). It can be anticipated that these complexes upon further modification could replace noble-metals in coming years owing to their inexpensiveness, physicochemical tunability and industrial-scale compatibility. This review comprehensively consolidates and analyses the latest advances in copper-based molecular electrocatalysts for the HER, mainly featuring homogeneous complexes composed of polydentate N-donor, N/S-donor and N/O-donor ligands, as well as molecular precursors that are converted into catalytically active heterogeneous Cu species during electrolysis. It further meticulously summarizes various strategic ligand engineering approaches through proton-responsive functional groups and bioinspired coordination motifs, allowing technologically relevant catalytic performances featuring mainly turnover frequencies exceeding 104 s−1 and faradaic efficiencies approaching 98% across pH of ∼2–14. Beyond performance metrics, this review dives deep into mechanistic insights resulting from kinetic analyses, spectroelectrochemical studies, and density functional theory calculations to explicate proton-coupled electron transfer (PCET) pathways involving transient Cu-hydride intermediates or ligand-assisted protonation steps that optimize adsorption–desorption energetics for faster kinetics. Particular emphasis is placed on the technological translation of molecular catalysts into practical systems, including catalyst immobilization on conductive substrates, molecular-to-heterogeneous catalyst transformation and integration within electrode architectures relevant to overall water electrolyzers. Crucial challenges such as catalyst stability, structural evolution under operating conditions and the need for standardized benchmarking protocols are explicitly discussed. Collectively, this review provides a roadmap for rationally designing robust Cu-molecular electrocatalysts and highlights their potential to enable cost-effective and scalable green H2 production technologies through electrolysis.

Abstract Image

铜基分子配合物:绿色析氢反应的新一代电催化剂
电化学水分解是可持续绿色制氢的一项关键技术,但其大规模运行需要具有低过电位和耐久性的高效电催化剂。在这种情况下,铜基分子配合物是电催化绿色析氢反应(HER)领域的新兴催化剂,具有广阔的应用前景。可以预见,这些配合物经过进一步改性后,由于其廉价、物理化学可调性和工业规模的兼容性,在未来几年内可以取代贵金属。本文综合分析了近年来国内外铜基电催化剂的研究进展,主要包括由多齿N给体、N/ s给体和N/ o给体组成的均相配合物,以及在电解过程中转化为具有催化活性的非均相Cu的分子前体。它进一步通过质子响应官能团和生物启发的配位基序精心总结了各种战略配体工程方法,允许技术相关的催化性能,主要是周转频率超过104 s−1,法拉第效率在pH为~ 2-14时接近98%。除了性能指标之外,本文还深入探讨了动力学分析、光谱电化学研究和密度泛函理论计算所产生的机制见解,以阐明质子耦合电子转移(PCET)途径,包括瞬态cu -氢化物中间体或配体辅助质子化步骤,优化吸附-脱附能量,以获得更快的动力学。特别强调的是分子催化剂到实际系统的技术转化,包括催化剂在导电基底上的固定化,分子到异相催化剂的转化以及与整个水电解槽相关的电极结构中的集成。关键的挑战,如催化剂的稳定性,在操作条件下的结构演变和需要标准化的基准协议进行了明确的讨论。总的来说,这篇综述为合理设计稳健的cu分子电催化剂提供了路线图,并强调了它们通过电解实现成本效益和可扩展的绿色氢气生产技术的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Sustainable Energy & Fuels
Sustainable Energy & Fuels Energy-Energy Engineering and Power Technology
CiteScore
10.00
自引率
3.60%
发文量
394
期刊介绍: Sustainable Energy & Fuels will publish research that contributes to the development of sustainable energy technologies with a particular emphasis on new and next-generation technologies.
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