Low‐Electronegativity Mn‐Contraction of PtMn Nanodendrites Boosts Oxygen Reduction Durability

Author:

Nie Yan12ORCID,Sun Yingjun1,Song Bingyi3,Meyer Quentin2,Liu Shiyang2,Guo Hongyu1,Tao Lu1,Lin Fangxu1,Luo Mingchuan1,Zhang Qinghua4,Gu Lin4,Yang Liming3ORCID,Zhao Chuan2ORCID,Guo Shaojun1ORCID

Affiliation:

1. School of Materials Science and Engineering Peking University Beijing 100871 China

2. School of Chemistry University of New South Wales Sydney 2052 Australia

3. Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Key Laboratory of Bioinorganic Chemistry and Materia Medica Hubei Key Laboratory of Materials Chemistry and Service Failure Hubei Engineering Research Center for Biomaterials and Medical Protective Materials School of Chemistry and Chemical Engineering Huazhong University of Science and Technology Wuhan 430074 China

4. Beijing National Laboratory for Condensed Matter Physics Institute of Physics Chinese Academy of Sciences Beijing 100190 P. R. China

Abstract

AbstractPlatinum metal (PtM, M=Ni, Fe, Co) alloys catalysts show high oxygen reduction reaction (ORR) activity due to their well‐known strain and ligand effects. However, these PtM alloys usually suffer from a deficient ORR durability in acidic environment as the alloyed metal is prone to be dissolved due to its high electronegativity. Herein, we report a new class of PtMn alloy nanodendrite catalyst with low‐electronegativity Mn‐contraction for boosting the oxygen reduction durability of fuel cells. The moderate strain in PtMn, induced by Mn contraction, yields optimal oxygen reduction activity at 0.53 A mg−1 at 0.9 V versus reversible hydrogen electrode (RHE). Most importantly, we show that relative to well‐known high‐electronegativity Ni‐based Pt alloy counterpart, the PtMn nanodendrite catalyst experiences less transition metals’ dissolution in acidic solution and achieves an outstanding mass activity retention of 96 % after 10,000 degradation cycles. Density functional theory calculation reveals that PtMn alloys are thermodynamically more stable than PtNi alloys in terms of formation enthalpy and cohesive energy. The PtMn nanodendrite‐based membrane electrode assembly delivers an outstanding peak power density of 1.36 W cm−2 at a low Pt loading and high‐performance retention over 50 h operations at 0.6 V in H2‐O2 hydrogen fuel cells.

Funder

National Key Research and Development Program of China

National Science Fund for Distinguished Young Scholars

Australian Research Council

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

General Chemistry,Catalysis

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