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表面带有纳米管的氮掺杂碳空心纳米十二面体负载的镍单原子/铁氮纳米颗粒用于将CO高效电还原为CO。

Ni Single Atoms/FeN Nanoparticles Supported by N-Doped Carbon Hollow Nanododecahedras with Nanotubes on the Surface for Efficient Electro-Reduction of CO to CO.

作者信息

Zhan Qi-Ni, Zhang Hong, Huang Chen-Jin, Xu Hui-Min, Shuai Ting-Yu, Zhu Hong-Rui, Li Gao-Ren

机构信息

College of Materials Science and Engineering, Sichuan University, Chengdu, 610065, China.

Yunnan Key Laboratory of Electromagnetic Materials and Devices, National Center for International Research on Photoelectric and Energy Materials, School of Materials and Energy, Yunnan University, Kunming, 650091, China.

出版信息

Small. 2025 Feb;21(7):e2410723. doi: 10.1002/smll.202410723. Epub 2025 Jan 23.

Abstract

The transition metal single atoms (SAs)-based catalysts with M-N coordination environment have shown excellent performance in electrocatalytic reduction of CO, and they have received extensive attention in recent years. However, the presence of SAs makes it very difficult to efficiently improve the coordination environment. In this paper, a method of direct high-temperature pyrolysis carbonization of ZIF-8 adsorbed with Ni and Fe ions is reported for the synthesis of Ni SAs and FeN nanoparticles (NPs) supported by the N-doped carbon (NC) hollow nanododecahedras (HNDs) with nanotubes (NTs) on the surface (Ni SAs/FeN NPs@NC-HNDs-NTs). The synergistic effect between Ni SAs and FeN NPs can obviously improve the proton-coupled electron transfer step of CO reduction reaction and promotes the process of electrocatalytic reduction of CO to CO. The fabricated Ni SAs/FeN NPs@NC-HNDs-NTs exhibits a high CO selectivity of up to 94% in the potential range of -0.41--0.81 V versus Reversible Hydrogen Electrode (vs RHE), and an optimal CO Faraday efficiency (FE) of ≈97.31% at -0.68 V (vs RHE) in the reduction reaction CO to CO. In the theoretical calculation results, due to the non-bonding synergy effect between Ni SAs and FeN NPs, the free energy of COOH formation is greatly reduced and the adsorption of CO is obviously improved, which will efficiently promote the conversion between the intermediates in the reaction step and accelerate electro-reduction process of CO. This work will provide a new method for constructing a mutually optimized coordination environment between Ni SAs and FeN NPs to improve the catalytic performance of CORR by synergistic complementarity between the dual active sites.

摘要

具有M-N配位环境的过渡金属单原子(SAs)基催化剂在电催化CO还原方面表现出优异的性能,近年来受到广泛关注。然而,SAs的存在使得有效改善配位环境变得非常困难。本文报道了一种通过直接高温热解碳化吸附有Ni和Fe离子的ZIF-8来合成由表面带有纳米管(NTs)的N掺杂碳(NC)中空纳米十二面体(HNDs)负载的Ni SAs和FeN纳米颗粒(NPs)的方法(Ni SAs/FeN NPs@NC-HNDs-NTs)。Ni SAs和FeN NPs之间的协同效应能够显著改善CO还原反应的质子耦合电子转移步骤,并促进CO电催化还原为CO的过程。制备的Ni SAs/FeN NPs@NC-HNDs-NTs在相对于可逆氢电极(vs RHE)为-0.41--0.81 V的电位范围内表现出高达94%的高CO选择性,并且在CO还原为CO的反应中,在-0.68 V(vs RHE)时具有约97.31%的最佳CO法拉第效率(FE)。在理论计算结果中,由于Ni SAs和FeN NPs之间的非键协同效应,COOH形成的自由能大大降低,CO的吸附明显改善,这将有效地促进反应步骤中中间体之间的转化,并加速CO的电还原过程。这项工作将为构建Ni SAs和FeN NPs之间相互优化的配位环境提供一种新方法,以通过双活性位点之间的协同互补来提高CORR的催化性能。

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