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      Synergizing Hydrogen Spillover and Deprotonation by the Internal Polarization Field in a MoS 2/NiPS 3 Vertical Heterostructure for Boosted Water Electrolysis

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          Abstract

          Hydrogen spillover (HSo) has emerged to upgrade the hydrogen evolution reaction (HER) activity of Pt‐support electrocatalysts, but it is not applicable to the deprotonated oxygen evolution reaction (OER). Non‐precious catalysts that can perform well in both HSo and deprotonation (DeP) are extremely desirable for a sustainable hydrogen economy. Herein, an affordable MoS 2/NiPS 3 vertical heterostructure catalyst is presented to synergize HSo and DeP for efficient water electrolysis. The internal polarization field (IPF) is clarified as the driving force of HSo in HER electrocatalysis. The HSo from the MoS 2 edge to NiPS 3 can activate the NiPS 3 basal plane to boost the HER activity of the MoS 2/NiPS 3 heterostructure (112 mV vs reversible hydrogen electrode (RHE) at 10 mA cm –2), while for OER, the IPF in the heterostructure can facilitate the hydroxyl diffusion and render MoS 2‐to‐NiPS 3/P‐to‐S dual‐pathways for DeP. As a result, the stacking of OER‐inactive MoS 2 on the NiPS 3 surface still brings intriguing OER enhancements. With them serving as electrode couples, the overall water splitting is attested stably with a cell voltage of 1.64 V at 10 mA cm −2. This research puts forward the IPF as the criterion in the rational design of HSo/DeP‐unified non‐precious catalysts for efficient water electrolysis.

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          General synthesis and definitive structural identification of MN4C4 single-atom catalysts with tunable electrocatalytic activities

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            A review on fundamentals for designing oxygen evolution electrocatalysts

            The fundamentals related to the oxygen evolution reaction and catalyst design are summarized and discussed. Electricity-driven water splitting can facilitate the storage of electrical energy in the form of hydrogen gas. As a half-reaction of electricity-driven water splitting, the oxygen evolution reaction (OER) is the major bottleneck due to the sluggish kinetics of this four-electron transfer reaction. Developing low-cost and robust OER catalysts is critical to solving this efficiency problem in water splitting. The catalyst design has to be built based on the fundamental understanding of the OER mechanism and the origin of the reaction overpotential. In this article, we summarize the recent progress in understanding OER mechanisms, which include the conventional adsorbate evolution mechanism (AEM) and lattice-oxygen-mediated mechanism (LOM) from both theoretical and experimental aspects. We start with the discussion on the AEM and its linked scaling relations among various reaction intermediates. The strategies to reduce overpotential based on the AEM and its derived descriptors are then introduced. To further reduce the OER overpotential, it is necessary to break the scaling relation of HOO* and HO* intermediates in conventional AEM to go beyond the activity limitation of the volcano relationship. Strategies such as stabilization of HOO*, proton acceptor functionality, and switching the OER pathway to LOM are discussed. The remaining questions on the OER and related perspectives are also presented at the end.
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              Engineering the electronic structure of single atom Ru sites via compressive strain boosts acidic water oxidation electrocatalysis

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                Author and article information

                Contributors
                Journal
                Advanced Materials
                Advanced Materials
                Wiley
                0935-9648
                1521-4095
                September 2022
                August 12 2022
                September 2022
                : 34
                : 37
                Affiliations
                [1 ] State Key Laboratory for Mechanical Behavior of Materials Xi'an Jiaotong University Xi'an 710049 P. R. China
                [2 ] MIIT Key Laboratory of Advanced Display Materials and Devices College of Materials Science and Engineering Nanjing University of Science and Technology Nanjing 210094 P. R. China
                Article
                10.1002/adma.202203615
                35900215
                e9168bb1-178b-4529-93af-b8c71147618f
                © 2022

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

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