Synthesis of PtNi Nanoparticles to Accelerate the Oxygen Reduction Reaction

被引:0
|
作者
Leteba, Gerard M. [1 ,3 ]
George, Sarah L. [1 ]
Mitchell, David R. G. [2 ]
Levecque, Pieter B. J. [3 ]
van Steen, Eric [3 ]
Macheli, Lebohang [4 ]
Lang, Candace I. [1 ]
机构
[1] Univ Cape Town, Ctr Mat Engn, Dept Mech Engn, ZA-7700 Cape Town, South Africa
[2] Univ Wollongong, Electron Microscopy Ctr, Innovat Campus, Wollongong, NSW 2517, Australia
[3] Univ Cape Town, Catalysis Inst, Dept Chem Engn, ZA-7700 Cape Town, South Africa
[4] Univ South Africa, Dept Chem Engn, Florida Campus, ZA-1710 Johannesburg, South Africa
来源
CHEMPLUSCHEM | 2024年 / 89卷 / 07期
基金
澳大利亚研究理事会;
关键词
PtNi NPs; ternary surfactants; thermal decomposition; electrocatalysts; ORR; CO MONOLAYER OXIDATION; CATALYTIC-ACTIVITY; PLATINUM; NANOCRYSTALS; ALLOY; ELECTROCATALYSTS; ELECTRODES; STRAIN; AREA;
D O I
10.1002/cplu.202400083
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the synthesis of core-shell Ni-Pt nanoparticles (NPs) with varying degrees of crystallographic facets and surface layers rich in Pt via a seed-mediated thermolytic approach. Mixtures of different surfactants used during synthesis resulted in preferential surface passivation, which in turn dictated the size, chemical composition, and geometric evolution of these PtNi NPs. Electrochemical investigations of these pristine core-shell Ni-Pt structures in the oxygen reduction reaction (ORR) show that their catalytic functionalities outperform the commercial Pt/C reference catalyst. The enhanced electrocatalytic ORR performances of these Pt-based PtNi NPs are correlated with the weakened oxygen binding strength or surface-adsorbed hydroxyl (OH) species on active Pt surface sites induced by the downshift of the d-band center as a result of compressive strain effects. Our studies offer a robust synthetic approach for the development of core-shell nanostructures for enhanced ORR catalysis. Highly efficient ORR electrocatalysts: PtNi NPs were solution-derived using a seed-growth thermolytic approach and a range of surfactants. These NPs exhibited outer surface layers rich in Pt (<= 1 nm) thickness displayed a significantly enhanced oxygen reduction reaction (ORR) when benchmarked against the commercial Pt/C catalyst. These improvements in electrocatalytic ORR performances are correlated with the weakened oxygen binding strength or surface-adsorbed hydroxyl (OH) species on active Pt surface sites, which is in turn induced by a downshift of the d-band center as a result of compressive strain effects. image
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页数:9
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