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      Highly durable iron single-atom catalysts for low-temperature zinc-air batteries by electronic regulation of adjacent iron nanoclusters

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          General synthesis and definitive structural identification of MN4C4 single-atom catalysts with tunable electrocatalytic activities

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            Enhanced electron penetration through an ultrathin graphene layer for highly efficient catalysis of the hydrogen evolution reaction.

            Major challenges encountered when trying to replace precious-metal-based electrocatalysts of the hydrogen evolution reaction (HER) in acidic media are related to the low efficiency and stability of non-precious-metal compounds. Therefore, new concepts and strategies have to be devised to develop electrocatalysts that are based on earth-abundant materials. Herein, we report a hierarchical architecture that consists of ultrathin graphene shells (only 1-3 layers) that encapsulate a uniform CoNi nanoalloy to enhance its HER performance in acidic media. The optimized catalyst exhibits high stability and activity with an onset overpotential of almost zero versus the reversible hydrogen electrode (RHE) and an overpotential of only 142 mV at 10 mA cm(-2) , which is quite close to that of commercial 40 % Pt/C catalysts. Density functional theory (DFT) calculations indicate that the ultrathin graphene shells strongly promote electron penetration from the CoNi nanoalloy to the graphene surface. With nitrogen dopants, they synergistically increase the electron density on the graphene surface, which results in superior HER activity on the graphene shells.
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              Defect Engineering toward Atomic Co–N x –C in Hierarchical Graphene for Rechargeable Flexible Solid Zn‐Air Batteries

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                Author and article information

                Contributors
                Journal
                Applied Catalysis B: Environmental
                Applied Catalysis B: Environmental
                Elsevier BV
                09263373
                April 2023
                April 2023
                : 323
                : 122163
                Article
                10.1016/j.apcatb.2022.122163
                f4da8dc3-1a47-46d5-a2fa-8e11ff2b0c47
                © 2023

                https://www.elsevier.com/tdm/userlicense/1.0/

                http://www.elsevier.com/open-access/userlicense/1.0/

                https://doi.org/10.15223/policy-017

                https://doi.org/10.15223/policy-037

                https://doi.org/10.15223/policy-012

                https://doi.org/10.15223/policy-029

                https://doi.org/10.15223/policy-004

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