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      Hierarchical Metal–[Carbon Nitride Shell/Carbon Core] Electrocatalysts: A Promising New General Approach to Tackle the ORR Bottleneck in Low-Temperature Fuel Cells

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          Most cited references35

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          Activity benchmarks and requirements for Pt, Pt-alloy, and non-Pt oxygen reduction catalysts for PEMFCs

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            Understanding Catalytic Activity Trends in the Oxygen Reduction Reaction

            Despite the dedicated search for novel catalysts for fuel cell applications, the intrinsic oxygen reduction reaction (ORR) activity of materials has not improved significantly over the past decade. Here, we review the role of theory in understanding the ORR mechanism and highlight the descriptor-based approaches that have been used to identify catalysts with increased activity. Specifically, by showing that the performance of the commonly studied materials (e.g., metals, alloys, carbons, etc.) is limited by unfavorable scaling relationships (for binding energies of reaction intermediates), we present a number of alternative strategies that may lead to the design and discovery of more promising materials for ORR.
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              Tuning the activity of Pt alloy electrocatalysts by means of the lanthanide contraction.

              The high platinum loadings required to compensate for the slow kinetics of the oxygen reduction reaction (ORR) impede the widespread uptake of low-temperature fuel cells in automotive vehicles. We have studied the ORR on eight platinum (Pt)-lanthanide and Pt-alkaline earth electrodes, Pt5M, where M is lanthanum, cerium, samarium, gadolinium, terbium, dysprosium, thulium, or calcium. The materials are among the most active polycrystalline Pt-based catalysts reported, presenting activity enhancement by a factor of 3 to 6 over Pt. The active phase consists of a Pt overlayer formed by acid leaching. The ORR activity versus the bulk lattice parameter follows a high peaked "volcano" relation. We demonstrate how the lanthanide contraction can be used to control strain effects and tune the activity, stability, and reactivity of these materials.
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                Author and article information

                Journal
                ACS Catal
                ACS Catal
                cs
                accacs
                ACS Catalysis
                American Chemical Society
                2155-5435
                27 September 2022
                07 October 2022
                : 12
                : 19
                : 12291-12301
                Affiliations
                []Section of Chemistry for the Technology (ChemTech), Department of Industrial Engineering, University of Padova , Via Marzolo 9, I-35131 Padova, Italy
                []National Interuniversity Consortium of Materials Science and Technology (INSTM) , Via Giusti, 9, I-50121 Firenze, Italy
                [§ ]Consiglio Nazionale delle Ricerche, Istituto di Chimica della Materia Condensata e di Tecnologie per l’Energia , Corso Stati Uniti 4, I-35127 Padova, Italy
                Author notes
                Author information
                https://orcid.org/0000-0002-8030-6979
                https://orcid.org/0000-0001-5253-8468
                https://orcid.org/0000-0002-4015-6670
                Article
                10.1021/acscatal.2c03723
                9552968
                36249870
                4c147a61-ac90-4d39-b3d0-552b7f8c7251
                © 2022 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 29 July 2022
                Funding
                Funded by: H2020 Future and Emerging Technologies, doi 10.13039/100010664;
                Award ID: 881603
                Funded by: Ministero dell’Istruzione, dell’Università e della Ricerca, doi 10.13039/501100003407;
                Award ID: FISR 2019
                Funded by: EIT RawMaterials, doi 10.13039/100019625;
                Award ID: ALPE - 19247
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                cs2c03723
                cs2c03723

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