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Single-Atom Catalysts for Selective Oxygen Reduction: Transition Metals in Uniform Carbon Nanospheres with High Loadings.
Jeskey, Jacob; Ding, Yong; Chen, Yidan; Hood, Zachary D; Sterbinsky, George E; Jaroniec, Mietek; Xia, Younan.
Afiliação
  • Jeskey J; School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
  • Ding Y; School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
  • Chen Y; School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
  • Hood ZD; Applied Materials Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.
  • Sterbinsky GE; Advanced Photon Source, Argonne National Laboratory, Lemont, Illinois 60439, United States.
  • Jaroniec M; Department of Chemistry and Biochemistry, Kent State University, Kent, Ohio 44242, United States.
  • Xia Y; School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
JACS Au ; 3(11): 3227-3236, 2023 Nov 27.
Article em En | MEDLINE | ID: mdl-38034958
ABSTRACT
Transition metal single-atom catalysts (SACs) in uniform carbon nanospheres have gained tremendous interest as electrocatalysts owing to their low cost, high activity, and excellent selectivity. However, their preparation typically involves complicated multistep processes that are not practical for industrial use. Herein, we report a facile one-pot method to produce atomically isolated metal atoms with high loadings in uniform carbon nanospheres without any templates or postsynthesis modifications. Specifically, we use a chemical confinement strategy to suppress the formation of metal nanoparticles by introducing ethylenediaminetetraacetic acid (EDTA) as a molecular barrier to spatially isolate the metal atoms and thus generate SACs. To demonstrate the versatility of this synthetic method, we produced SACs from multiple transition metals, including Fe, Co, Cu, and Ni, with loadings as high as 3.87 wt %. Among these catalytic materials, the Fe-based SACs showed remarkable catalytic activity toward the oxygen reduction reaction (ORR), achieving an onset and half-wave potential of 1.00 and 0.831 VRHE, respectively, comparable to that of commercial 20 wt % Pt/C. Significantly, we were able to steer the ORR selectivity toward either energy generation or hydrogen peroxide production by simply changing the transition metal in the EDTA-based precursor.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JACS Au Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JACS Au Ano de publicação: 2023 Tipo de documento: Article