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通过将镍铁合金纳米颗粒封装在氮掺杂碳纳米纤维中来增强析氧反应活性

Enhanced Oxygen Evolution Reaction Activity by Encapsulating NiFe Alloy Nanoparticles in Nitrogen-Doped Carbon Nanofibers.

作者信息

Wei Peng, Sun Xueping, Liang Qirui, Li Xiaogang, He Zhimin, Hu Xiangsheng, Zhang Jinxu, Wang Minhui, Li Qing, Yang Hui, Han Jiantao, Huang Yunhui

机构信息

Department of Mechanics, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China.

School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China.

出版信息

ACS Appl Mater Interfaces. 2020 Jul 15;12(28):31503-31513. doi: 10.1021/acsami.0c08271. Epub 2020 Jul 6.

DOI:10.1021/acsami.0c08271
PMID:32569458
Abstract

The rational design and exploration of the oxygen evolution reaction (OER) electrocatalysts with high efficiency, low cost, and long-term durability are extremely important for overall water splitting. Recently, numerous studies have shown that the OER reaction kinetics can be modified by optimizing components, introducing carbon matrix, and regulating porous nanostructures. Herein, a flexible and controllable electrospinning strategy is proposed to construct porous nitrogen (N)-doped carbon (C) nanofibers (NFs) with nickel-iron (NiFe) alloy nanoparticles encapsulated inside (NiFe@NCNFs) as an OER electrocatalyst. Benefiting from the strong synergistic effects that stem from the one-dimensional mesoporous structures with optimized binary metal components encapsulated in the N-doped carbon nanofibers, the NiFe@NCNFs exhibits enhanced OER performance with a low overpotential (294 mV at 10 mA cm) and excellent durability (over 10 h at 10 mA cm) in alkaline solution. Both experimental characterizations and density functional theory (DFT) calculations validate that a suitable binary metal ratio can lead to the optimal catalytic activity. Moreover, a two-electrode electrolyzer is assembled by using NiFe@NCNFs anode and Pt/C cathode in 1.0 M KOH media for the overall water splitting, which delivers an initial cell voltage of only 1.531 V at 10 mA cm, as well as long-term stability up to 20 h. This study sheds light on the design and large-scale production of low-cost and high-performance electrocatalysts toward different energy applications in the future.

摘要

合理设计和探索具有高效率、低成本和长期耐久性的析氧反应(OER)电催化剂对于全水分解极为重要。最近,大量研究表明,通过优化组分、引入碳基体和调控多孔纳米结构可以改善OER反应动力学。在此,我们提出一种灵活可控的静电纺丝策略来构建多孔氮(N)掺杂碳(C)纳米纤维(NFs),其内部包裹有镍铁(NiFe)合金纳米颗粒(NiFe@NCNFs)作为OER电催化剂。受益于一维介孔结构与包裹在氮掺杂碳纳米纤维中的优化二元金属组分所产生的强协同效应,NiFe@NCNFs在碱性溶液中表现出增强的OER性能,具有低过电位(10 mA cm时为294 mV)和优异的耐久性(10 mA cm下超过10小时)。实验表征和密度泛函理论(DFT)计算均证实,合适的二元金属比例可导致最佳催化活性。此外,在1.0 M KOH介质中使用NiFe@NCNFs阳极和Pt/C阴极组装了两电极电解槽用于全水分解,在10 mA cm时初始电池电压仅为1.531 V,并且具有长达20小时的长期稳定性。该研究为未来面向不同能源应用的低成本高性能电催化剂的设计和大规模生产提供了思路。

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