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      Comparative Study of the Structure, Composition, and Electrocatalytic Performance of Hydrogen Evolution in MoS x ~2+δ/Mo and MoS x~ 3+δ Films Obtained by Pulsed Laser Deposition

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          Abstract

          Systematic and in-depth studies of the structure, composition, and efficiency of hydrogen evolution reactions (HERs) in MoS x films, obtained by means of on- and off-axis pulsed laser deposition (PLD) from a MoS 2 target, have been performed. The use of on-axis PLD (a standard configuration of PLD) in a buffer of Ar gas, with an optimal pressure, has allowed for the formation of porous hybrid films that consist of Mo particles which support a thin MoS x ~2+δ (δ of ~0.7) film. The HER performance of MoS x ~2+δ/Mo films increases with increased loading and reaches the highest value at a loading of ~240 μg/cm 2. For off-axis PLD, the substrate was located along the axis of expansion of the laser plume and the film was formed via the deposition of the atomic component of the plume, which was scattered in Ar molecules. This made it possible to obtain homogeneous MoS x ~3+δ (δ~0.8–1.1) films. The HER performances of these films reached saturation at a loading value of ~163 μg/cm 2. The MoS x ~3+δ films possessed higher catalytic activities in terms of the turnover frequency of their HERs. However, to achieve the current density of 10 mA/cm 2, the lowest over voltages were −162 mV and −150 mV for the films obtained by off- and on-axis PLD, respectively. Measurements of electrochemical characteristics indicated that the differences in the achievable HER performances of these films could be caused by their unique morphological properties.

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          Amorphous molybdenum sulfide films as catalysts for electrochemical hydrogen production in water

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            Building an appropriate active-site motif into a hydrogen-evolution catalyst with thiomolybdate [Mo3S13]2- clusters.

            Identifying and understanding the active sites responsible for reaction turnover is critical to developing improved catalysts. For the hydrogen-evolution reaction (HER), MoS2 has been identified as an active non-noble-metal-based catalyst. However, only edge sites turnover the reaction because the basal planes are catalytically inert. In an effort to develop a scalable HER catalyst with an increased number of active sites, herein we report a Mo-S catalyst (supported thiomolybdate [Mo3S13](2-) nanoclusters) in which most sulfur atoms in the structure exhibit a structural motif similar to that observed at MoS2 edges. Supported sub-monolayers of [Mo3S13](2-) nanoclusters exhibited excellent HER activity and stability in acid. Imaging at the atomic scale with scanning tunnelling microscopy allowed for direct characterization of these supported catalysts. The [Mo3S13](2-) nanoclusters reported herein demonstrated excellent turnover frequencies, higher than those observed for other non-precious metal catalysts synthesized by a scalable route.
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              Recent Development in Hydrogen Evolution Reaction Catalysts and Their Practical Implementation.

              The past 10 years have seen great advances in the field of electrochemical hydrogen evolution. In particular, several new nonprecious metal electrocatalysts, for example, the MoS2 or the Ni2P family of materials, have emerged as contenders for electrochemical hydrogen evolution under harsh acidic conditions offering nearly platinum-like catalytic performance. The developments have been particularly fast in the last 5 years, and the present Perspective highlights key developments and discusses them, along with hydrogen evolution in general, in the context of the global energy problem.
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                Author and article information

                Journal
                Nanomaterials (Basel)
                Nanomaterials (Basel)
                nanomaterials
                Nanomaterials
                MDPI
                2079-4991
                24 January 2020
                February 2020
                : 10
                : 2
                : 201
                Affiliations
                [1 ]Moscow Engineering Physics Institute, National Research Nuclear University MEPhI (Moscow Engineering Physics Institute), 115409 Moscow, Russia; dmitryfominski@ 123456gmail.com (D.F.); limpo2003@ 123456mail.ru (R.R.)
                [2 ]Russia Immanuel Kant Baltic Federal University, 236016 Kaliningrad, Russia; sterlad@ 123456mail.ru (M.D.); aygoikhman@ 123456gmail.com (A.G.); xmaksimova@ 123456gmail.com (K.M.)
                Author notes
                [* ]Correspondence: vyfominskij@ 123456mephi.ru
                Author information
                https://orcid.org/0000-0001-9179-8991
                Article
                nanomaterials-10-00201
                10.3390/nano10020201
                7074935
                31991546
                5ca9c7fa-d4a0-431e-9371-1518bf31015f
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 02 December 2019
                : 22 January 2020
                Categories
                Article

                pulsed laser deposition,nanocatalysts,buffer gas,transition metal chalcogenides,hydrogen evolution reaction

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