Boron induced strong metal-support interaction for high sintering resistance of Pt-based catalysts toward oxygen reduction reaction
[Display omitted] •Synthesis of ultrasmall Pt NPs with improved sintering resistance.•Boron doping into carbon contributes to the enhanced metal-support interaction.•The method is extended to prepare PtM (M = Co, Fe, Ni, Cu) alloy NPs.•The catalysts exhibit enhanced ORR activity and stability. Insuf...
Saved in:
Published in | Applied surface science Vol. 604; p. 154466 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.12.2022
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | [Display omitted]
•Synthesis of ultrasmall Pt NPs with improved sintering resistance.•Boron doping into carbon contributes to the enhanced metal-support interaction.•The method is extended to prepare PtM (M = Co, Fe, Ni, Cu) alloy NPs.•The catalysts exhibit enhanced ORR activity and stability.
Insufficient thermal and electrochemical stability is a large challenge for carbon-supported Pt-based nanoparticles (NPs) as oxygen reduction reaction (ORR) catalysts. Herein, a facile pyrolysis method is developed for the synthesis of ultrasmall Pt NPs anchored on boron-doped carbon (Pt/(B-C)). The stronger interaction between Pt and boron-doped carbon (B-C) endows catalysts with improved sintering resistance to stabilize the Pt NPs of sub-3 nm up to 700 °C. The Pt/(B-C)600 catalyst presents a mass activity (MA) of 0.30 A mgPt−1, which is 3 times that of commercial Pt/C (0.10 A mgPt−1). After durability test, the MA of the Pt/(B-C)600 catalyst has only decreased by 19.7% (commercial Pt/C dropped by 58.7%). This method can also be extended to prepare B-C supported Pt alloy NPs (PtM/(B-C), M = Co, Fe, Ni, Cu), which exhibit superior ORR performance. This study provides a general strategy for the synthesis of thermally and electrochemically stable carbon supported Pt-based catalysts. |
---|---|
ISSN: | 0169-4332 1873-5584 |
DOI: | 10.1016/j.apsusc.2022.154466 |