Highly active, selective, and stable Pd single-atom catalyst anchored on N-doped hollow carbon sphere for electrochemical H2O2 synthesis under acidic conditions
- Authors
- Xi, Jiangbo; Yang, Sungeun; Silvioli, Luca; Cao, Sufeng; Liu, Pei; Chen, Qiongyang; Zhao, Yanyan; Sun, Hongyu; Hansen, Johannes Novak; Haraldsted, Jens-Peter B.; Kibsgaard, Jakob; Rossmeisl, Jan; Bals, Sara; Wang, Shuai; Chorkendorff, Ib
- Issue Date
- 2021-01
- Publisher
- ACADEMIC PRESS INC ELSEVIER SCIENCE
- Citation
- JOURNAL OF CATALYSIS, v.393, pp.313 - 323
- Abstract
- Single-atom catalysts (SACs) have recently attracted broad scientific interests due to their unique structural feature, the single-atom dispersion. Optimized electronic structure as well as high stability are required for single-atom catalysts to enable efficient electrochemical production of H2O2. Herein, we report a facile synthesis method that stabilizes atomic Pd species on the reduced graphene oxide/Ndoped carbon hollow carbon nanospheres (Pd1/N-C). Pd1/N-C exhibited remarkable electrochemical H2O2 production rate with high faradaic efficiency, reaching 80%. The single-atom structure and its high H2O2 production rate were maintained even after 10,000 cycle stability test. The existence of single-atom Pd as well as its coordination with N species is responsible for its high activity, selectivity, and stability. The N coordination number and substrate doping around Pd atoms are found to be critical for an optimized adsorption energy of intermediate *OOH, resulting in efficient electrochemical H2O2 production. (C) 2020 Elsevier Inc. All rights reserved.
- Keywords
- HYDROGEN-PEROXIDE; OXYGEN REDUCTION; IRON; NANOPARTICLES; COORDINATION; INTERFACE; OXIDATION; EFFICIENT; GRAPHENE; SITES; Single-atom catalyst; Nitrogen doped carbon; Hydrogen peroxide; Electrochemical synthesis; Density functional theory
- ISSN
- 0021-9517
- URI
- https://pubs.kist.re.kr/handle/201004/117578
- DOI
- 10.1016/j.jcat.2020.11.020
- Appears in Collections:
- KIST Article > 2021
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