4.8 Article

Nanosized Metal Phosphides Embedded in Nitrogen-Doped Porous Carbon Nanofibers for Enhanced Hydrogen Evolution at All pH Values

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 57, Issue 7, Pages 1963-1967

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201710150

Keywords

hydrogen evolution reaction; nitrogen-doped; porous carbon; transition-metal phosphides

Funding

  1. National Natural Science Foundation of China [21773188]
  2. Fundamental Research Funds for the Central Universities [XDJK2017D003, XDJK2017B055]
  3. Program for Excellent Talents in Chongqing [102060-20600218]
  4. Program for Innovation Team Building at Institutions of Higher Education in Chongqing [CXTDX201601011]
  5. Chongqing Key Laboratory for Advanced Materials and Technologies

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Transition-metal phosphides (TMPs) have emerged as promising catalyst candidates for the hydrogen evolution reaction (HER). Although numerous methods have been investigated to obtain TMPs, most rely on traditional synthetic methods that produce materials that are inherently deficient with respect to electrical conductivity. An electrospinning-based reduction approach is presented, which generates nickel phosphide nanoparticles in N-doped porous carbon nanofibers (Ni2P@NPCNFs) in situ. Ni2P nanoparticles are protected from irreversible fusion and aggregation in subsequent high-temperature pyrolysis. The resistivity of Ni2P@NPCNFs (5.34 Omega cm) is greatly decreased by 10(4) times compared to Ni2P (> 10(4) Omega cm) because N-doped carbon NFs are incorporated. As an electrocatalyst for HER, Ni2P@NPCNFs reveal remarkable performance compared to other previously reported catalysts in acidic media. Additionally, it offers excellent catalytic ability and durability in both neutral and basic media. Encouraged by the excellent electrocatalytic performance of Ni2P@NPCNFs, a series of pea-like MxP@NPCNFs, including Fe2P@NPCNFs, Co2P@NPCNFs, and Cu3P@NPCNFs, were synthesized by the same method. Detailed characterization suggests that the newly developed method could render combinations of ultrafine metal phosphides with porous carbon accessible; thereby, extending opportunities in electrocatalytic applications.

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