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用于高效、耐用且经济的析氢反应的极化碳-镍催化表面的构建

Construction of Polarized Carbon-Nickel Catalytic Surfaces for Potent, Durable, and Economic Hydrogen Evolution Reactions.

作者信息

Zhou Min, Weng Qunhong, Popov Zakhar I, Yang Yijun, Antipina Liubov Yu, Sorokin Pavel B, Wang Xi, Bando Yoshio, Golberg Dmitri

机构信息

College of Physical Science and Technology, Institute of Optoelectronic Technology , Yangzhou University , Yangzhou 225002 , China.

International Center for Materials Nanoarchitectonics (MANA) , National Institute for Materials Science (NIMS) , Namiki 1-1 , Tsukuba 305-0044 , Japan.

出版信息

ACS Nano. 2018 May 22;12(5):4148-4155. doi: 10.1021/acsnano.7b08724. Epub 2018 Mar 20.

Abstract

Electrocatalytic hydrogen evolution reaction (HER) in alkaline solution is hindered by its sluggish kinetics toward water dissociation. Nickel-based catalysts, as low-cost and effective candidates, show great potentials to replace platinum (Pt)-based materials in the alkaline media. The main challenge regarding this type of catalysts is their relatively poor durability. In this work, we conceive and construct a charge-polarized carbon layer derived from carbon quantum dots (CQDs) on NiN nanostructure (NiN@CQDs) surfaces, which simultaneously exhibit durable and enhanced catalytic activity. The NiN@CQDs shows an overpotential of 69 mV at a current density of 10 mA cm in a 1 M KOH aqueous solution, lower than that of Pt electrode (116 mV) at the same conditions. Density functional theory (DFT) simulations reveal that NiN and interfacial oxygen polarize charge distributions between originally equal C-C bonds in CQDs. The partially negatively charged C sites become effective catalytic centers for the key water dissociation step via the formation of new C-H bond (Volmer step) and thus boost the HER activity. Furthermore, the coated carbon is also found to protect interior NiN from oxidization/hydroxylation and therefore guarantees its durability. This work provides a practical design of robust and durable HER electrocatalysts based on nonprecious metals.

摘要

碱性溶液中的电催化析氢反应(HER)因其对水离解的缓慢动力学而受到阻碍。镍基催化剂作为低成本且有效的候选材料,在碱性介质中显示出取代铂(Pt)基材料的巨大潜力。这类催化剂面临的主要挑战是其耐久性相对较差。在这项工作中,我们构思并构建了一种源自碳量子点(CQDs)的电荷极化碳层,该碳层位于NiN纳米结构(NiN@CQDs)表面,同时展现出持久且增强的催化活性。在1 M KOH水溶液中,NiN@CQDs在电流密度为10 mA cm时的过电位为69 mV,低于相同条件下Pt电极的过电位(116 mV)。密度泛函理论(DFT)模拟表明,NiN和界面氧使CQDs中原本等同的C - C键之间的电荷分布发生极化。部分带负电的C位点通过形成新的C - H键(Volmer步骤)成为关键水离解步骤的有效催化中心,从而提高了析氢反应活性。此外,还发现包覆的碳可保护内部的NiN不被氧化/羟基化,因此保证了其耐久性。这项工作为基于非贵金属的稳健且持久的析氢反应电催化剂提供了一种切实可行的设计。

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