TY - JOUR
T1 - Ordered Pt3Mn Intermetallic Nanoparticles Supported on Atomically Dispersed Mn–N–C as Electrocatalysts for Fuel Cells
AU - Chen, Gongjin
AU - Wang, Tianshuai
AU - Qiu, Xiaoyi
AU - Liu, Shiyuan
AU - Li, Cunpu
AU - Wei, Zidong
AU - Xing, Wei
AU - Wang, Haijiang
AU - Shao, Minhua
N1 - Publisher Copyright:
© 2026 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.
PY - 2026
Y1 - 2026
N2 - Compared with conventional solid-solution alloy nanoparticles with disordered atomic structures, platinum (Pt)-based intermetallic compounds (IMCs) are recognized as highly promising electrocatalysts for practical fuel cell applications, on account of their long-range periodically ordered atomic arrangements. Nevertheless, the rational development of Pt-based catalysts featuring both high intrinsic activity and long-term durability remains a key challenge in this field. In this work, by simultaneously introducing manganese (Mn) with low-electronegativity into both the active component and the support, we report an efficient electrocatalyst toward the oxygen reduction reaction (ORR), composed of L12-ordered Pt3Mn nanoparticles on Mn single-atom nitrogen-doped carbon support (L12-Pt3Mn@Mn–N–C). The incorporation of Mn, the strong anchoring effect arising from the hierarchically porous structure of the support, and the directional interfacial electron transfer between L12-Pt3Mn and Mn–N–C synergistically mitigate the adsorption strength of key oxygen intermediates and suppress the dissolution of surface Pt sites. Superior catalytic performance and durability are validated in proton exchange membrane fuel cells (PEMFCs), achieving a peak power density of 1.15 W cm−2 under H2/air conditions. After 30 000 square-wave cycles, the voltage loss at 0.8 A cm−2 is only 19 mV, ranking it among the top-performing Pt-based cathode catalysts reported to date.
AB - Compared with conventional solid-solution alloy nanoparticles with disordered atomic structures, platinum (Pt)-based intermetallic compounds (IMCs) are recognized as highly promising electrocatalysts for practical fuel cell applications, on account of their long-range periodically ordered atomic arrangements. Nevertheless, the rational development of Pt-based catalysts featuring both high intrinsic activity and long-term durability remains a key challenge in this field. In this work, by simultaneously introducing manganese (Mn) with low-electronegativity into both the active component and the support, we report an efficient electrocatalyst toward the oxygen reduction reaction (ORR), composed of L12-ordered Pt3Mn nanoparticles on Mn single-atom nitrogen-doped carbon support (L12-Pt3Mn@Mn–N–C). The incorporation of Mn, the strong anchoring effect arising from the hierarchically porous structure of the support, and the directional interfacial electron transfer between L12-Pt3Mn and Mn–N–C synergistically mitigate the adsorption strength of key oxygen intermediates and suppress the dissolution of surface Pt sites. Superior catalytic performance and durability are validated in proton exchange membrane fuel cells (PEMFCs), achieving a peak power density of 1.15 W cm−2 under H2/air conditions. After 30 000 square-wave cycles, the voltage loss at 0.8 A cm−2 is only 19 mV, ranking it among the top-performing Pt-based cathode catalysts reported to date.
KW - electrocatalysis
KW - fuel cells
KW - intermetallic compounds
KW - oxygen reduction reaction
KW - single-atom
UR - https://www.scopus.com/pages/publications/105041277478
U2 - 10.1002/anie.7818348
DO - 10.1002/anie.7818348
M3 - 文章
AN - SCOPUS:105041277478
SN - 1433-7851
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
ER -