中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Uniform Pd0.33Ir0.67 nanoparticles supported on nitrogen-doped carbon with remarkable activity toward the alkaline hydrogen oxidation reaction

文献类型:期刊论文

作者Yu, Hongmei3; Yi, Baolian3; Cong, Yuanyuan2,3,4; McCrum, Ian T.4,5; Song, Yujiang2,4; Gao, Xueqiang3,6; Janik, Michael J.4,5; Lv, Yang2,4; Miao, Shu1; Shao, Zhigang3
刊名JOURNAL OF MATERIALS CHEMISTRY A
出版日期2019-02-21
卷号7期号:7页码:3161-3169
ISSN号2050-7488
DOI10.1039/c8ta11019k
通讯作者Yu, Hongmei(hmyu@dicp.ac.cn) ; Janik, Michael J.(mjanik@psu.edu) ; Song, Yujiang(yjsong@dlut.edu.cn)
英文摘要Highly efficient non-Pt electrocatalysts for the alkaline hydrogen oxidation reaction (HOR) are required to enable complete replacement of Pt in hydroxide exchange membrane fuel cells (HEMFCs). Herein, we report a facile synthesis of a series of 2.4-2.9 nm Pd1-xIrx (x = 0.33, 0.50, 0.67, 0.75, 0.80, 0.91) alloy nanoparticles (NPs) evenly distributed on nitrogen-doped carbon (N-C) via simple chemical reduction of aqueous metallic complexes by sodium borohydride (NaBH4) in the absence of surfactants. The Ir component of alloy NPs and the nitrogen dopants of the carbon matrix contribute to the particle size control and uniform distribution. Remarkably, the resultant Pd0.33Ir0.67/N-C exhibits an exceptional alkaline HOR activity, measured as mass specific exchange current density (j(0,m)), that is 1.4 times that of commercial Pt/C. CO stripping shows that Pd0.33Ir0.67/N-C has an electrochemical active surface area (ECSA) of 106 m(2) g(metal)(-1) that is 1.2 times that of commercial Pt/C, partially explaining the increased activity. Furthermore, density functional theory (DFT) demonstrates an appropriate strength of hydrogen binding of Pd0.33Ir0.67, which is consistent with cyclic voltammetry (CV) measurements. In addition, DFT shows that Pd0.33Ir0.67 possesses the highest oxophilic property among all of the Pd1-xIrx electrocatalysts. We conclude that the high ECSA, appropriate strength of hydrogen binding, and the strong oxophilic property collectively account for the remarkable activity of Pd0.33Ir0.67/N-C. The latter two factors should be closely correlated with the electronic effect between Pd and Ir as evidenced by Xray photoelectron spectroscopy (XPS). A single cell fabricated with Pd0.33Ir0.67/N-C as the anode approaches a peak power density of 514 mW cm(-2) that is 1.3 times that of commercial Pt/C. This study demonstrates the substitution of commercial Pt/C with a non-Pt electrocatalyst at the anode of the single cell of HEMFCs with enhanced performance.
WOS关键词HIGH-PERFORMANCE ; EVOLUTION REACTION ; EXCHANGE ; CATALYSTS ; DURABILITY ; ACID ; ELECTROCATALYSTS ; MECHANISM ; PH ; ELECTROLYTES
资助项目National Key Research & Development Program of China[2016YFB0101307] ; Liaoning BaiQianWan Talents Program[201519] ; Program for Liaoning Excellent Talents in University[LR2015014] ; Dalian Excellent Young Scientific and Technological Talents[2015R006]
WOS研究方向Chemistry ; Energy & Fuels ; Materials Science
语种英语
出版者ROYAL SOC CHEMISTRY
WOS记录号WOS:000458682100021
资助机构National Key Research & Development Program of China ; National Key Research & Development Program of China ; Liaoning BaiQianWan Talents Program ; Liaoning BaiQianWan Talents Program ; Program for Liaoning Excellent Talents in University ; Program for Liaoning Excellent Talents in University ; Dalian Excellent Young Scientific and Technological Talents ; Dalian Excellent Young Scientific and Technological Talents ; National Key Research & Development Program of China ; National Key Research & Development Program of China ; Liaoning BaiQianWan Talents Program ; Liaoning BaiQianWan Talents Program ; Program for Liaoning Excellent Talents in University ; Program for Liaoning Excellent Talents in University ; Dalian Excellent Young Scientific and Technological Talents ; Dalian Excellent Young Scientific and Technological Talents ; National Key Research & Development Program of China ; National Key Research & Development Program of China ; Liaoning BaiQianWan Talents Program ; Liaoning BaiQianWan Talents Program ; Program for Liaoning Excellent Talents in University ; Program for Liaoning Excellent Talents in University ; Dalian Excellent Young Scientific and Technological Talents ; Dalian Excellent Young Scientific and Technological Talents ; National Key Research & Development Program of China ; National Key Research & Development Program of China ; Liaoning BaiQianWan Talents Program ; Liaoning BaiQianWan Talents Program ; Program for Liaoning Excellent Talents in University ; Program for Liaoning Excellent Talents in University ; Dalian Excellent Young Scientific and Technological Talents ; Dalian Excellent Young Scientific and Technological Talents
源URL[http://cas-ir.dicp.ac.cn/handle/321008/165982]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
通讯作者Yu, Hongmei; Song, Yujiang; Janik, Michael J.
作者单位1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
2.Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, 2 Linggong Rd, Dalian 116024, Peoples R China
3.Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Syst & Engn Lab, Dalian 116023, Peoples R China
4.Dalian Univ Technol, Penn State & DUT Joint Ctr Energy Res, 2 Linggong Rd, Dalian 116024, Peoples R China
5.Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
6.Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100039, Peoples R China
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Yu, Hongmei,Yi, Baolian,Cong, Yuanyuan,et al. Uniform Pd0.33Ir0.67 nanoparticles supported on nitrogen-doped carbon with remarkable activity toward the alkaline hydrogen oxidation reaction[J]. JOURNAL OF MATERIALS CHEMISTRY A,2019,7(7):3161-3169.
APA Yu, Hongmei.,Yi, Baolian.,Cong, Yuanyuan.,McCrum, Ian T..,Song, Yujiang.,...&Shao, Zhigang.(2019).Uniform Pd0.33Ir0.67 nanoparticles supported on nitrogen-doped carbon with remarkable activity toward the alkaline hydrogen oxidation reaction.JOURNAL OF MATERIALS CHEMISTRY A,7(7),3161-3169.
MLA Yu, Hongmei,et al."Uniform Pd0.33Ir0.67 nanoparticles supported on nitrogen-doped carbon with remarkable activity toward the alkaline hydrogen oxidation reaction".JOURNAL OF MATERIALS CHEMISTRY A 7.7(2019):3161-3169.

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来源:大连化学物理研究所

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