Quinary, Senary, and Septenary High Entropy Alloy Nanoparticle Catalysts from Core@Shell Nanoparticles and the Significance of Intraparticle Heterogeneity

被引:65
作者
Bueno, Sandra L. A. [1 ]
Leonardi, Alberto [2 ,3 ]
Kar, Nabojit [1 ]
Chatterjee, Kaustav [1 ]
Zhan, Xun [1 ]
Chen, Changqiang [4 ]
Wang, Zhiyu
Engel, Michael [3 ]
Fung, Victor [5 ]
Skrabalak, Sara E. [1 ]
机构
[1] Indiana Univ Bloomington, Dept Chem, Bloomington, IN 47405 USA
[2] ISIS Neutron & Muon Facil, UKRI Sci & Tech Facil Council, Didcot OX11 0YJ, Oxfordshire, England
[3] Friedrich Alexander Univ Erlangen Nuremberg, Inst Multiscale Simulat, IZNF, D-91058 Erlangen, Germany
[4] Univ Illinois, Mat Res Lab, Illinois united States, Urbana, IL USA
[5] Georgia Inst Technol, Sch Computat Sci & Engn, Atlanta, GA 30332 USA
关键词
higher order alloys; nanoparticles; colloidal methods; phase transformations; catalysis; oxygen reduction reaction; TOTAL-ENERGY CALCULATIONS; OXYGEN REDUCTION; PROGRESS;
D O I
10.1021/acsnano.2c07787
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Colloidally prepared core@shell nanoparticles (NPs) were converted to monodisperse high entropy alloy (HEA) NPs by annealing, including quinary, senary, and septenary phases comprised of PdCuPtNi with Co, Ir, Rh, Fe, and/or Ru. Intraparticle heterogeneity, i.e., subdomains within individual NPs with different metal distributions, was observed for NPs containing Ir and Ru, with the phase stabilities of the HEAs studied by atomistic simulations. The quinary HEA NPs were found to be durable catalysts for the oxygen reduction reaction, with all but the PdCuPtNiIr NPs presenting better activities than commercial Pt. Density functional theory (DFT) calculations for PdCuPtNiCo and PdCuPtNiIr surfaces (the two extremes in performance) found agreement with experiment by weighting the adsorption energy contributions by the probabilities of each active site based on their DFT energies. This finding highlights how intraparticle heterogeneity, which we show is likely overlooked in many systems due to analytical limitations, can be leveraged toward efficient catalysis.
引用
收藏
页码:18873 / 18885
页数:13
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