Ultrahigh Mass Activity Pt Entities Consisting of Pt Single atoms, Clusters, and Nanoparticles for Improved Hydrogen Evolution Reaction

Author:

Zeng Zhiqiang12ORCID,Küspert Sven12ORCID,Balaghi S. Esmael23,Hussein Haytham E. M.4,Ortlieb Niklas13,Knäbbeler‐Buß Markus5,Hügenell Philipp5,Pollitt Stephan6,Hug Niclas1,Melke Julia123,Fischer Anna123ORCID

Affiliation:

1. Institute of Inorganic and Analytical Chemistry (IAAC) University of Freiburg Albertstraße 21 79104 Freiburg Germany

2. Freiburg Materials Research Center (FMF) University of Freiburg Stefan‐Meier‐Straße 21 79104 Freiburg Germany

3. Freiburg Center for Interactive Materials and Bioinspired Technologies (FIT) University of Freiburg Georges‐Köhler‐Allee 105 79110 Freiburg Germany

4. Department of Chemistry University of Warwick Coventry CV4 7AL UK

5. The Fraunhofer Institute for Solar Energy Systems ISE Heidenhofstraße 2 79110 Freiburg Germany

6. Paul Scherrer Institute Forschungsstrasse 111, Villigen PSI Villigen 5232 Switzerland

Abstract

AbstractPlatinum is one of the best‐performing catalysts for the hydrogen evolution reaction (HER). However, high cost and scarcity severely hinder the large‐scale application of Pt electrocatalysts. Constructing highly dispersed ultrasmall Platinum entities is thereby a very effective strategy to increase Pt utilization and mass activities, and reduce costs. Herein, highly dispersed Pt entities composed of a mixture of Pt single atoms, clusters, and nanoparticles are synthesized on mesoporous N‐doped carbon nanospheres. The presence of Pt single atoms, clusters, and nanoparticles is demonstrated by combining among others aberration‐corrected annular dark‐field scanning transmission electron microscopy, X‐ray absorption spectroscopy, and electrochemical CO stripping. The best catalyst exhibits excellent geometric and Pt HER mass activity, respectively ≈4 and 26 times higher than that of a commercial Pt/C reference and a Pt catalyst supported on nonporous N‐doped carbon nanofibers with similar Pt loadings. Noteworthily, after optimization of the geometrical Pt electrode loading, the best catalyst exhibits ultrahigh Pt and catalyst mass activities (56 ± 3 A mg−1Pt and 11.7 ± 0.6 A mg−1Cat at −50 mV vs. reversible hydrogen electrode), which are respectively ≈1.5 and 58 times higher than the highest Pt and catalyst mass activities for Pt single‐atom and cluster‐based catalysts reported so far.

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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