9
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Principles of Water Electrolysis and Recent Progress in Cobalt‐, Nickel‐, and Iron‐Based Oxides for the Oxygen Evolution Reaction

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Water electrolysis that results in green hydrogen is the key process towards a circular economy. The supply of sustainable electricity and availability of oxygen evolution reaction (OER) electrocatalysts are the main bottlenecks of the process for large‐scale production of green hydrogen. A broad range of OER electrocatalysts have been explored to decrease the overpotential and boost the kinetics of this sluggish half‐reaction. Co‐, Ni‐, and Fe‐based catalysts have been considered to be potential candidates to replace noble metals due to their tunable 3d electron configuration and spin state, versatility in terms of crystal and electronic structures, as well as abundance in nature. This Review provides some basic principles of water electrolysis, key aspects of OER, and significant criteria for the development of the catalysts. It provides also some insights on recent advances of Co‐, Ni‐, and Fe‐based oxides and a brief perspective on green hydrogen production and the challenges of water electrolysis.

          Abstract

          This Review describes the basic principles of water electrolysis, key aspects of the oxygen evolution reaction (OER), and significant criteria for the development of new catalysts. Recent advances in catalysts based on Co, Ni, and Fe oxides are described, and a brief perspective is given on green hydrogen production and the challenges of water electrolysis.

          Related collections

          Most cited references193

          • Record: found
          • Abstract: found
          • Article: not found

          Combining theory and experiment in electrocatalysis: Insights into materials design

          Electrocatalysis plays a central role in clean energy conversion, enabling a number of sustainable processes for future technologies. This review discusses design strategies for state-of-the-art heterogeneous electrocatalysts and associated materials for several different electrochemical transformations involving water, hydrogen, and oxygen, using theory as a means to rationalize catalyst performance. By examining the common principles that govern catalysis for different electrochemical reactions, we describe a systematic framework that clarifies trends in catalyzing these reactions, serving as a guide to new catalyst development while highlighting key gaps that need to be addressed. We conclude by extending this framework to emerging clean energy reactions such as hydrogen peroxide production, carbon dioxide reduction, and nitrogen reduction, where the development of improved catalysts could allow for the sustainable production of a broad range of fuels and chemicals.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            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.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Electrocatalysis for the oxygen evolution reaction: recent development and future perspectives

              We review the fundamental aspects of metal oxides, metal chalcogenides and metal pnictides as effective electrocatalysts for the oxygen evolution reaction. There is still an ongoing effort to search for sustainable, clean and highly efficient energy generation to satisfy the energy needs of modern society. Among various advanced technologies, electrocatalysis for the oxygen evolution reaction (OER) plays a key role and numerous new electrocatalysts have been developed to improve the efficiency of gas evolution. Along the way, enormous effort has been devoted to finding high-performance electrocatalysts, which has also stimulated the invention of new techniques to investigate the properties of materials or the fundamental mechanism of the OER. This accumulated knowledge not only establishes the foundation of the mechanism of the OER, but also points out the important criteria for a good electrocatalyst based on a variety of studies. Even though it may be difficult to include all cases, the aim of this review is to inspect the current progress and offer a comprehensive insight toward the OER. This review begins with examining the theoretical principles of electrode kinetics and some measurement criteria for achieving a fair evaluation among the catalysts. The second part of this review acquaints some materials for performing OER activity, in which the metal oxide materials build the basis of OER mechanism while non-oxide materials exhibit greatly promising performance toward overall water-splitting. Attention of this review is also paid to in situ approaches to electrocatalytic behavior during OER, and this information is crucial and can provide efficient strategies to design perfect electrocatalysts for OER. Finally, the OER mechanism from the perspective of both recent experimental and theoretical investigations is discussed, as well as probable strategies for improving OER performance with regards to future developments.
                Bookmark

                Author and article information

                Contributors
                tueysuez@kofo.mpg.de
                Journal
                Angew Chem Int Ed Engl
                Angew Chem Int Ed Engl
                10.1002/(ISSN)1521-3773
                ANIE
                Angewandte Chemie (International Ed. in English)
                John Wiley and Sons Inc. (Hoboken )
                1433-7851
                1521-3773
                21 July 2021
                03 January 2022
                : 61
                : 1 ( doiID: 10.1002/anie.v61.1 )
                : e202103824
                Affiliations
                [ 1 ] Department of Heterogeneous Catalysis Max-Planck-Institute für Kohlenforschung Kaiser-Wilhelm-Platz 1 45470 Mülheim an der Ruhr Germany
                Author information
                http://orcid.org/0000-0001-6184-8863
                http://orcid.org/0000-0001-8552-7028
                Article
                ANIE202103824
                10.1002/anie.202103824
                9291824
                34138511
                a3611a25-25f7-4dcd-8499-697865ded236
                © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 17 March 2021
                Page count
                Figures: 19, Tables: 1, References: 208, Pages: 24, Words: 0
                Funding
                Funded by: Max-Planck-Gesellschaft , doi 10.13039/501100004189;
                Funded by: Deutsche Forschungsgemeinschaft , doi 10.13039/501100001659;
                Award ID: Projektnummer 388390466-TRR 247 within the Collaborative Research Centre/Transregio 247 "Heterogeneous Oxidation Catalysis in the Liquid Phase
                Categories
                Review
                Reviews
                Water Electrolysis
                Custom metadata
                2.0
                January 3, 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.7 mode:remove_FC converted:18.07.2022

                Chemistry
                cobalt,iron,nickel,oxygen evolution reaction,water splitting
                Chemistry
                cobalt, iron, nickel, oxygen evolution reaction, water splitting

                Comments

                Comment on this article