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      Facet Engineering of Advanced Electrocatalysts Toward Hydrogen/Oxygen Evolution Reactions

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          Highlights

          • The crystal facets featured with facet-dependent physical and chemical properties can exhibit varied electrocatalytic activity toward hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) attributed to their anisotropy.

          • The highly active exposed crystal facets enable increased mass activity of active sites, lower reaction energy barriers, and enhanced catalytic reaction rates for HER and OER.

          • The formation mechanism and control strategy of the crystal facet, significant contributions as well as challenges and perspectives of facet-engineered catalysts for HER and OER are provided.

          Abstract

          The electrocatalytic water splitting technology can generate high-purity hydrogen without emitting carbon dioxide, which is in favor of relieving environmental pollution and energy crisis and achieving carbon neutrality. Electrocatalysts can effectively reduce the reaction energy barrier and increase the reaction efficiency. Facet engineering is considered as a promising strategy in controlling the ratio of desired crystal planes on the surface. Owing to the anisotropy, crystal planes with different orientations usually feature facet-dependent physical and chemical properties, leading to differences in the adsorption energies of oxygen or hydrogen intermediates, and thus exhibit varied electrocatalytic activity toward hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). In this review, a brief introduction of the basic concepts, fundamental understanding of the reaction mechanisms as well as key evaluating parameters for both HER and OER are provided. The formation mechanisms of the crystal facets are comprehensively overviewed aiming to give scientific theory guides to realize dominant crystal planes. Subsequently, three strategies of selective capping agent, selective etching agent, and coordination modulation to tune crystal planes are comprehensively summarized. Then, we present an overview of significant contributions of facet-engineered catalysts toward HER, OER, and overall water splitting. In particular, we highlight that density functional theory calculations play an indispensable role in unveiling the structure–activity correlation between the crystal plane and catalytic activity. Finally, the remaining challenges in facet-engineered catalysts for HER and OER are provided and future prospects for designing advanced facet-engineered electrocatalysts are discussed.

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          Most cited references229

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          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.
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            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.
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              Noble metal-free hydrogen evolution catalysts for water splitting.

              Sustainable hydrogen production is an essential prerequisite of a future hydrogen economy. Water electrolysis driven by renewable resource-derived electricity and direct solar-to-hydrogen conversion based on photochemical and photoelectrochemical water splitting are promising pathways for sustainable hydrogen production. All these techniques require, among many things, highly active noble metal-free hydrogen evolution catalysts to make the water splitting process more energy-efficient and economical. In this review, we highlight the recent research efforts toward the synthesis of noble metal-free electrocatalysts, especially at the nanoscale, and their catalytic properties for the hydrogen evolution reaction (HER). We review several important kinds of heterogeneous non-precious metal electrocatalysts, including metal sulfides, metal selenides, metal carbides, metal nitrides, metal phosphides, and heteroatom-doped nanocarbons. In the discussion, emphasis is given to the synthetic methods of these HER electrocatalysts, the strategies of performance improvement, and the structure/composition-catalytic activity relationship. We also summarize some important examples showing that non-Pt HER electrocatalysts could serve as efficient cocatalysts for promoting direct solar-to-hydrogen conversion in both photochemical and photoelectrochemical water splitting systems, when combined with suitable semiconductor photocatalysts.
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                Author and article information

                Contributors
                zhangqian5689@njfu.edu.cn
                youbo@hust.edu.cn
                weichen@ciac.ac.cn
                shuijianhe@njfu.edu.cn
                Journal
                Nanomicro Lett
                Nanomicro Lett
                Nano-Micro Letters
                Springer Nature Singapore (Singapore )
                2311-6706
                2150-5551
                16 February 2023
                16 February 2023
                December 2023
                : 15
                : 52
                Affiliations
                [1 ]GRID grid.410625.4, ISNI 0000 0001 2293 4910, International Innovation Center for Forest Chemicals and Materials, Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, , Nanjing Forestry University, ; Nanjing, 210037 People’s Republic of China
                [2 ]GRID grid.33199.31, ISNI 0000 0004 0368 7223, Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, , Huazhong University of Science and Technology (HUST), ; Wuhan, 430074 People’s Republic of China
                [3 ]GRID grid.440652.1, ISNI 0000 0004 0604 9016, Institute of Materials Science and Devices, School of Materials Science and Engineering, , Suzhou University of Science and Technology, ; Suzhou, 2150009 People’s Republic of China
                [4 ]GRID grid.459584.1, ISNI 0000 0001 2196 0260, Guangxi Key Laboratory of Low Carbon Energy Materials, College of Chemistry and Pharmaceutical Sciences, , Guangxi Normal University, ; Guilin, 541004 People’s Republic of China
                [5 ]GRID grid.9227.e, ISNI 0000000119573309, State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, , Chinese Academy of Sciences, ; Changchun, 130022 People’s Republic of China
                [6 ]GRID grid.59053.3a, ISNI 0000000121679639, University of Science and Technology of China, ; Hefei, 230026 People’s Republic of China
                Article
                1024
                10.1007/s40820-023-01024-6
                9935811
                36795218
                f543130b-9dc3-41a4-8e45-37a44df0d48e
                © The Author(s) 2023

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 9 November 2022
                : 4 January 2023
                Funding
                Funded by: Shanghai Jiao Tong University
                Categories
                Review
                Custom metadata
                © The Author(s) 2023

                crystal facet engineering,anisotropy,oxygen evolution reaction,hydrogen evolution reaction,theoretical simulations

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