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      Rational engineering design of nickel hydroxides for urea oxidation reaction: A mini-review

      , , , ,
      Electrochemistry Communications
      Elsevier BV

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          Electrocatalytic oxygen evolution reaction for energy conversion and storage: A comprehensive review

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            2D Layered Double Hydroxides for Oxygen Evolution Reaction: From Fundamental Design to Application

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              The role of oxygen vacancies of ABO3 perovskite oxides in the oxygen reduction reaction

              The oxygen reduction reaction (ORR) is one of the most important electrochemical reactions in energy conversion and storage technologies, such as fuel cells and metal–air batteries. The oxygen reduction reaction (ORR) is one of the most important electrochemical reactions in energy conversion and storage technologies, such as fuel cells and metal–air batteries. However, the sluggish kinetics of the ORR is a key factor limiting the performance of these energy storage and conversion devices. Perovskite oxides are a promising family of electrocatalysts for the ORR because of their unique physical and chemical properties, such as variable crystal structure and non-stoichiometric chemistry. Studies have shown that the catalytic properties of perovskite oxides in the ORR are largely related to oxygen vacancies, which alter their electronic and crystal structures and surface chemistry. This review summarizes recent research advances on understanding the role of oxygen vacancies of the ABO 3 perovskite oxides in catalyzing the ORR. With a brief introduction of perovskite oxides, approaches to creating oxygen vacancies in the ABO 3 perovskite oxides and the role of oxygen vacancies in improving their catalytic performance for the ORR are discussed. Research perspectives in this important area are highlighted.
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                Author and article information

                Contributors
                Journal
                Electrochemistry Communications
                Electrochemistry Communications
                Elsevier BV
                13882481
                December 2023
                December 2023
                : 157
                : 107599
                Article
                10.1016/j.elecom.2023.107599
                c3efb5b0-cf02-45dc-9ee8-5eb1dbfb0be0
                © 2023

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

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

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