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      Understanding Advanced Transition Metal‐Based Two Electron Oxygen Reduction Electrocatalysts from the Perspective of Phase Engineering

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          Abstract

          Non‐noble transition metal (TM)‐based compounds have recently become a focal point of extensive research interest as electrocatalysts for the two electron oxygen reduction (2e ORR) process. To efficiently drive this reaction, these TM‐based electrocatalysts must bear unique physiochemical properties, which are strongly dependent on their phase structures. Consequently, adopting engineering strategies toward the phase structure has emerged as a cutting‐edge scientific pursuit, crucial for achieving high activity, selectivity, and stability in the electrocatalytic process. This comprehensive review addresses the intricate field of phase engineering applied to non‐noble TM‐based compounds for 2e ORR. First, the connotation of phase engineering and fundamental concepts related to oxygen reduction kinetics and thermodynamics are succinctly elucidated. Subsequently, the focus shifts to a detailed discussion of various phase engineering approaches, including elemental doping, defect creation, heterostructure construction, coordination tuning, crystalline design, and polymorphic transformation to boost or revive the 2e ORR performance (selectivity, activity, and stability) of TM‐based catalysts, accompanied by an insightful exploration of the phase‐performance correlation. Finally, the review proposes fresh perspectives on the current challenges and opportunities in this burgeoning field, together with several critical research directions for the future development of non‐noble TM‐based electrocatalysts.

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          Origin of the Overpotential for Oxygen Reduction at a Fuel-Cell Cathode

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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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              Defect Chemistry of Nonprecious-Metal Electrocatalysts for Oxygen Reactions.

              Oxygen electrocatalysis, including the oxygen-reduction reaction (ORR) and oxygen-evolution reaction (OER), is a critical process for metal-air batteries. Therefore, the development of electrocatalysts for the OER and the ORR is of essential importance. Indeed, various advanced electrocatalysts have been designed for the ORR or the OER; however, the origin of the advanced activity of oxygen electrocatalysts is still somewhat controversial. The enhanced activity is usually attributed to the high surface areas, the unique facet structures, the enhanced conductivities, or even to unclear synergistic effects, but the importance of the defects, especially the intrinsic defects, is often neglected. More recently, the important role of defects in oxygen electrocatalysis has been demonstrated by several groups. To make the defect effect clearer, the recent development of this concept is reviewed here and a novel principle for the design of oxygen electrocatalysts is proposed. An overview of the defects in carbon-based, metal-free electrocatalysts for ORR and various defects in metal oxides/selenides for OER is also provided. The types of defects and controllable strategies to generate defects in electrocatalysts are presented, along with techniques to identify the defects. The defect-activity relationship is also explored by theoretical methods.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Advanced Materials
                Advanced Materials
                Wiley
                0935-9648
                1521-4095
                June 2024
                March 25 2024
                June 2024
                : 36
                : 25
                Affiliations
                [1 ] Institute of Functional Nano and Soft Materials (FUNSOM) Jiangsu Key Laboratory for Carbon‐based Functional Materials and Devices Joint International Research Laboratory of Carbon‐Based Functional Materials and Devices Soochow University Suzhou 215123 P. R. China
                [2 ] Department of Chemistry: Metalorganics and Inorganic Materials Technische Universität Berlin Straße des 17 Juni 135, Sekr. C2 10623 Berlin Germany
                [3 ] Materials Chemistry Group for Thin Film Catalysis – CatLab Helmholtz‐Zentrum Berlin für Materialien und Energie Albert‐Einstein‐Str. 15 12489 Berlin Germany
                Article
                10.1002/adma.202400140
                4d5a3744-249b-427a-a643-77802c939d4f
                © 2024

                http://creativecommons.org/licenses/by/4.0/

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