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      Advances in Oxygen Evolution Electrocatalysts for Proton Exchange Membrane Water Electrolyzers

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          Abstract

          Proton exchange membrane water electrolyzer (PEMWE) technology is of interest in the context of electrocatalytic hydrogen generation from renewable energies. It has the benefits of immediate response, higher proton conductivity, lower ohmic losses, and gas crossover rate. One key step toward to large‐scale application, is the development of highly efficient, durable, and compatible anodic oxygen evolution electrocatalysts in acidic media to decrease the usage of expensive and scarce precious metals. Within this scenario, an in‐depth understanding of oxygen evolution reaction mechanisms including the adsorption evolution mechanism and lattice oxygen evolution mechanism is first provided to aid development of innovative materials and elucidate the origin of catalyst degradation. Second, recent progress in the development of oxygen evolution electrocatalysts in acid media is reviewed with an emphasis on the underlying structure–performance relationships. Third, the current application status and research progress in PEMWEs along with representative examples are discussed. Last, the remaining challenges and promising insights are proposed to inspire future studies on the development of hydrogen production technology from renewable energy.

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          A perovskite oxide optimized for oxygen evolution catalysis from molecular orbital principles.

          The efficiency of many energy storage technologies, such as rechargeable metal-air batteries and hydrogen production from water splitting, is limited by the slow kinetics of the oxygen evolution reaction (OER). We found that Ba(0.5)Sr(0.5)Co(0.8)Fe(0.2)O(3-δ) (BSCF) catalyzes the OER with intrinsic activity that is at least an order of magnitude higher than that of the state-of-the-art iridium oxide catalyst in alkaline media. The high activity of BSCF was predicted from a design principle established by systematic examination of more than 10 transition metal oxides, which showed that the intrinsic OER activity exhibits a volcano-shaped dependence on the occupancy of the 3d electron with an e(g) symmetry of surface transition metal cations in an oxide. The peak OER activity was predicted to be at an e(g) occupancy close to unity, with high covalency of transition metal-oxygen bonds.
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            Universality in Oxygen Evolution Electrocatalysis on Oxide Surfaces

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              A comprehensive review on PEM water electrolysis

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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Advanced Energy Materials
                Advanced Energy Materials
                Wiley
                1614-6832
                1614-6840
                April 2022
                February 17 2022
                April 2022
                : 12
                : 14
                Affiliations
                [1 ] Key Laboratory for Green Chemical Technology of the Ministry of Education School of Chemical Engineering and Technology Tianjin University Tianjin 300072 P. R. China
                [2 ] Collaborative Innovative Center of Chemical Science and Engineering (Tianjin) Tianjin 300072 P. R. China
                [3 ] Zhejiang Institute of Tianjin University Ningbo Zhejiang 315201 P. R. China
                Article
                10.1002/aenm.202103670
                b9d00c8f-0b01-4529-9f1f-9eb658257498
                © 2022

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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