Han Weiwei, Zhang Fan, Qiu Lingshu, Qian Yang, Hao Shaoyun, Li Ping, He Yi, Zhang Xingwang
Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, Zhejiang Province 310027, China.
Institute of Zhejiang University-Quzhou, Quzhou, Zhejiang Province 324000, China.
Nanoscale. 2022 Oct 27;14(41):15498-15506. doi: 10.1039/d2nr04657a.
The development of non-noble metal electrocatalysts with high activity and long-term stability for the hydrogen evolution reaction (HER), especially at large current density, is of great significance for industrial hydrogen production from water using renewable electricity. Constructing heterostructures with interfacial interactions is an effective strategy to improve the catalytic performance for large-current-density HER. Herein, we innovatively present a facile two-step electrodeposition method to immobilize a hierarchical NiCoP/NiCoS heterostructure on Ni foam (NF) for alkaline HER. The strong interfacial coupling effect between NiCoP and NiCoS not only offers abundant active sites for fast electrochemical reaction, but also enhances the charge transfer ability accompanied by high electrical conductivity. Consequently, the obtained self-supporting NiCoP/NiCoS/NF exhibits an excellent catalytic performance with low overpotentials of 68, 144 and 222 mV to deliver current densities of 10, 100 and 500 mA cm in 1 M KOH, along with good stability for more than 110 h, outperforming most of the reported non-noble metal based HER catalysts. Density functional theory (DFT) results further confirm that this bimetal phosphide/sulfide heterostructure can synergistically optimize the Gibbs free energy of H* during the HER process, thus accelerating the HER reaction kinetics. This work provides a new strategy toward the rational design of large-current-density electrocatalysts, which have great potential in practical large-scale hydrogen production.
开发具有高活性和长期稳定性的非贵金属电催化剂用于析氢反应(HER),尤其是在大电流密度下,对于利用可再生电力从水中进行工业制氢具有重要意义。构建具有界面相互作用的异质结构是提高大电流密度HER催化性能的有效策略。在此,我们创新性地提出一种简便的两步电沉积方法,将分级NiCoP/NiCoS异质结构固定在泡沫镍(NF)上用于碱性HER。NiCoP和NiCoS之间强烈的界面耦合效应不仅为快速电化学反应提供了丰富的活性位点,还增强了伴随高电导率的电荷转移能力。因此,所制备的自支撑NiCoP/NiCoS/NF表现出优异的催化性能,在1 M KOH中,电流密度分别为10、100和500 mA cm时,过电位低至68、144和222 mV,并且具有超过110 h的良好稳定性,优于大多数已报道的非贵金属基HER催化剂。密度泛函理论(DFT)结果进一步证实,这种双金属磷化物/硫化物异质结构在HER过程中可以协同优化H*的吉布斯自由能,从而加速HER反应动力学。这项工作为合理设计大电流密度电催化剂提供了一种新策略,在实际大规模制氢中具有巨大潜力。