Nitrogen-doped carbon-coated Ru nanoparticles as a highly efficient and stable electrocatalyst for alkaline hydrogen oxidation reaction

IF 5.5 3区 材料科学 Q1 ELECTROCHEMISTRY
Jianchao Yue, Pengyu Han, Xinyi Yang, Xiaoqin Ma, Yu Zhang, Liqing Wu, Jianchuan Wang, Wei Luo
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Abstract

Designing non-Pt-based electrocatalysts with high catalytic activity is challenging but extremely desirable for alkaline hydrogen oxidation reaction (HOR). Herein, we successfully design a nitrogen doped carbon shell coated Ru nanoparticles (Ru@NC) catalyst for efficient alkaline HOR. The obtained Ru@NC exhibits an excellent mass activity of 1.279 mA μgPGM-1, which is 8.1-times, 10.3-times and 3.7-times higher than that of Ru@C, Ru/C and commercial Pt/C. When further employed as the anode catalyst for anion exchange membrane fuel cell (AEMFC), a peak power density of 1.114 W cm-2 can be achieved for Ru@NC. Density functional theory (DFT) calculations and experimental results indicate that the hydroxyl binding energy (OHBE) is continually enhanced on the catalysts due to the encapsulation of carbon shell and nitrogen doping derived from the upshifted d-band center of Ru sites in catalysts, which is responsible for the enhanced alkaline HOR performance.

Abstract Image

氮掺杂碳包覆Ru纳米颗粒作为高效稳定的碱性氢氧化反应电催化剂
设计具有高催化活性的非pt基电催化剂是具有挑战性的,但也是碱性氢氧化反应(HOR)所迫切需要的。在此,我们成功设计了一种氮掺杂碳壳包覆的Ru纳米颗粒(Ru@NC)催化剂,用于高效的碱性HOR。所得Ru@NC的质量活性为1.279 mA μgPGM-1,分别是Ru@C、Ru/C和商用Pt/C的8.1倍、10.3倍和3.7倍。当进一步用作负离子交换膜燃料电池(AEMFC)的阳极催化剂时,Ru@NC的峰值功率密度可达到1.114 W cm-2。密度泛函理论(DFT)计算和实验结果表明,催化剂的羟基结合能(OHBE)不断增强,这是由于催化剂中Ru位点d波段中心上移导致的碳壳包封和氮掺杂导致的,这是增强碱性HOR性能的原因。
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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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