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We report a versatile method based on seed-mediated growth for the facile synthesis of trimetallic Pd@PtxAu1−x core-shell nanocubes. By simply varying the feeding ratio between the Pt(II) and Au(III) precursors, the atomic ratio of Pt to Au in the shell and thereby the ensemble state of Pt atoms on the surface can be tuned to control the binding configuration of O2 molecules. Specifically, discrete Pt atoms on the surface promote the adsorption of O2 molecules in the Pauling configuration to enhance the catalytic selectivity of the nanoparticles toward H2O2 via the two-electron oxygen reduction reaction, with the Pd@Pt0.025Au0.975 nanocubes showing selectivity as high as 91% at 0.45 VRHE. This work offers a viable means to augment the electrocatalytic performance of alloy nanocrystals by controlling their surface compositions.
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Highly Selective Oxygen Reduction to Hydrogen Peroxide on a Carbon-Supported Single-Atom Pd Electrocatalyst
Selective electrochemical two-electron oxygen reduction is a promising route for renewable and on-site H2O2 generation as an alternative to the anthraquinone process. Herein, we report a high-performance nitrogen-coordinated single-atom Pd electrocatalyst, which is derived from Pd-doped zeolitic imidazolate frameworks (ZIFs) through one-step thermolysis. High-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) combined with X-ray absorption spectroscopy verifies atomically dispersed Pd atoms on nitrogen-doped carbon (Pd-NC). The single-atom Pd-NC catalyst exhibits excellent electrocatalytic performance for two-electron oxygen reduction to H2O2, which shows ∼95% selectivity toward H2O2 and an unprecedented onset potential of ∼0.8 V versus revisable hydrogen electrode (RHE) in 0.1 M KOH. Density functional theory (DFT) calculations demonstrate that the Pd-N4 catalytic sites thermodynamically prefer *–O bond breaking to O–O bond breaking, corresponding to a high selectivity for H2O2 production. This work provides a deep insight into the understanding of the catalytic process and design of high-performance 2e– ORR catalysts.
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- PAR ID:
- 10319293
- Date Published:
- Journal Name:
- ACS Catalysis
- ISSN:
- 2155-5435
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1021/acscatal.1c05633
