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Seeded Synthesis of Unconventional 2H-Phase Pd Alloy Nanomaterials for Highly Efficient Oxygen Reduction.
Ge, Yiyao; Wang, Xixi; Huang, Biao; Huang, Zhiqi; Chen, Bo; Ling, Chongyi; Liu, Jiawei; Liu, Guanghua; Zhang, Jie; Wang, Gang; Chen, Ye; Li, Lujiang; Liao, Lingwen; Wang, Lei; Yun, Qinbai; Lai, Zhuangchai; Lu, Shiyao; Luo, Qinxin; Wang, Jinlan; Zheng, Zijian; Zhang, Hua.
Afiliação
  • Ge Y; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Wang X; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Huang B; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Huang Z; Hong Kong Branch of National Precious Metals Material Engineering Research Center (NPMM), City University of Hong Kong, Hong Kong, China.
  • Chen B; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Ling C; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Liu J; School of Physics, Southeast University, Nanjing 211189, China.
  • Liu G; Center for Programmable Materials, School of Materials Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.
  • Zhang J; State Key Laboratory of New Ceramics & Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China.
  • Wang G; State Key Laboratory of New Ceramics & Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China.
  • Chen Y; Department of Chemistry, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.
  • Li L; Department of Chemistry, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.
  • Liao L; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Wang L; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Yun Q; Laboratory for Advanced Interfacial Materials and Devices, Institution of Textiles and Clothing, Research Institute for Smart Energy, & Research Institute of Intelligent Wearable Systems, The Hong Kong Polytechnic University, Hung Hom, Hong Kong, China.
  • Lai Z; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Lu S; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Luo Q; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Wang J; Department of Chemistry, City University of Hong Kong, Hong Kong, China.
  • Zheng Z; School of Physics, Southeast University, Nanjing 211189, China.
  • Zhang H; Laboratory for Advanced Interfacial Materials and Devices, Institution of Textiles and Clothing, Research Institute for Smart Energy, & Research Institute of Intelligent Wearable Systems, The Hong Kong Polytechnic University, Hung Hom, Hong Kong, China.
J Am Chem Soc ; 143(41): 17292-17299, 2021 Oct 20.
Article em En | MEDLINE | ID: mdl-34613737
ABSTRACT
Crystal phase engineering of noble-metal-based alloy nanomaterials paves a new way to the rational synthesis of high-performance catalysts for various applications. However, the controlled preparation of noble-metal-based alloy nanomaterials with unconventional crystal phases still remains a great challenge due to their thermodynamically unstable nature. Herein, we develop a robust and general seeded method to synthesize PdCu alloy nanomaterials with unconventional hexagonal close-packed (hcp, 2H type) phase and also tunable Cu contents. Moreover, galvanic replacement of Cu by Pt can be further conducted to prepare unconventional trimetallic 2H-PdCuPt nanomaterials. Impressively, 2H-Pd67Cu33 nanoparticles possess a high mass activity of 0.87 A mg-1Pd at 0.9 V (vs reversible hydrogen electrode (RHE)) in electrochemical oxygen reduction reaction (ORR) under alkaline condition, which is 2.5 times that of the conventional face-centered cubic (fcc) Pd69Cu31 counterpart, revealing the important role of crystal phase on determining the ORR performance. After the incorporation of Pt, the obtained 2H-Pd71Cu22Pt7 catalyst shows a significantly enhanced mass activity of 1.92 A mg-1Pd+Pt at 0.9 V (vs RHE), which is 19.2 and 8.7 times those of commercial Pt/C and Pd/C, placing it among the best reported Pd-based ORR electrocatalysts under alkaline conditions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article