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      Heterostructuring Mesoporous 2D Iridium Nanosheets with Amorphous Nickel Boron Oxide Layers to Improve Electrolytic Water Splitting

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          Abstract

          2D heterostructures exhibit a considerable potential in electrolytic water splitting due to their high specific surface areas, tunable electronic properties, and diverse hybrid compositions. However, the fabrication of well‐defined 2D mesoporous amorphous‐crystalline heterostructures with highly active heterointerfaces remains challenging. Herein, an efficient 2D heterostructure consisting of amorphous nickel boron oxide (Ni‐B i ) and crystalline mesoporous iridium (meso‐Ir) is designed for water splitting, referred to as Ni‐B i /meso‐Ir. Benefiting from well‐defined 2D heterostructures and strong interfacial coupling, the resulting mesoporous dual‐phase Ni‐B i /meso‐Ir possesses abundant catalytically active heterointerfaces and boosts the exposure of active sites, compared to their crystalline and amorphous mono‐counterparts. The electronic state of the iridium sites is tuned favorably by hybridizing with Ni‐B i layers. Consequently, the Ni‐B i /meso‐Ir heterostructures show superior and stable electrochemical performance toward both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in an alkaline electrolyte.

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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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            Computational high-throughput screening of electrocatalytic materials for hydrogen evolution.

            The pace of materials discovery for heterogeneous catalysts and electrocatalysts could, in principle, be accelerated by the development of efficient computational screening methods. This would require an integrated approach, where the catalytic activity and stability of new materials are evaluated and where predictions are benchmarked by careful synthesis and experimental tests. In this contribution, we present a density functional theory-based, high-throughput screening scheme that successfully uses these strategies to identify a new electrocatalyst for the hydrogen evolution reaction (HER). The activity of over 700 binary surface alloys is evaluated theoretically; the stability of each alloy in electrochemical environments is also estimated. BiPt is found to have a predicted activity comparable to, or even better than, pure Pt, the archetypical HER catalyst. This alloy is synthesized and tested experimentally and shows improved HER performance compared with pure Pt, in agreement with the computational screening results.
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              Enhancing hydrogen evolution activity in water splitting by tailoring Li⁺-Ni(OH)₂-Pt interfaces.

              Improving the sluggish kinetics for the electrochemical reduction of water to molecular hydrogen in alkaline environments is one key to reducing the high overpotentials and associated energy losses in water-alkali and chlor-alkali electrolyzers. We found that a controlled arrangement of nanometer-scale Ni(OH)(2) clusters on platinum electrode surfaces manifests a factor of 8 activity increase in catalyzing the hydrogen evolution reaction relative to state-of-the-art metal and metal-oxide catalysts. In a bifunctional effect, the edges of the Ni(OH)(2) clusters promoted the dissociation of water and the production of hydrogen intermediates that then adsorbed on the nearby Pt surfaces and recombined into molecular hydrogen. The generation of these hydrogen intermediates could be further enhanced via Li(+)-induced destabilization of the HO-H bond, resulting in a factor of 10 total increase in activity.
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                Author and article information

                Contributors
                Journal
                Small Methods
                Small Methods
                Wiley
                2366-9608
                2366-9608
                October 2021
                September 2021
                October 2021
                : 5
                : 10
                Affiliations
                [1 ] Department of Nanoscience and Nanoengineering Department of Life Science and Medical Bioscience and Department of Applied Chemistry Faculty of Science and Engineering Waseda University Shinjuku Tokyo 169–8555 Japan
                [2 ] JST‐ERATO Yamauchi Materials Space‐Tectonics Project and International Center for Materials Nanoarchitectonics (WPI‐MANA) National Institute for Materials Science (NIMS) Tsukuba Ibaraki 305‐0044 Japan
                [3 ] The Education Ministry Key Lab of Resource Chemistry and Shanghai Key Laboratory of Rare Earth Functional Materials Shanghai Normal University Shanghai 200234 China
                [4 ] Electron Microscopy Group National Institute for Materials Science (NIMS) Tsukuba Ibaraki 305‐0044 Japan
                [5 ] Australian Institute for Bioengineering and Nanotechnology (AIBN) and School of Chemical Engineering The University of Queensland Brisbane QLD 4072 Australia
                [6 ] JST‐ERATO Yamauchi Materials Space‐Tectonics Project Kagami Memorial Research Institute for Materials Science and Technology Waseda University Shinjuku Tokyo 169‐0051 Japan
                Article
                10.1002/smtd.202100679
                7ff6a477-9e65-4738-b45b-d9b1586194f0
                © 2021

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