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      Atomic cobalt on nitrogen-doped graphene for hydrogen generation

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          Abstract

          Reduction of water to hydrogen through electrocatalysis holds great promise for clean energy, but its large-scale application relies on the development of inexpensive and efficient catalysts to replace precious platinum catalysts. Here we report an electrocatalyst for hydrogen generation based on very small amounts of cobalt dispersed as individual atoms on nitrogen-doped graphene. This catalyst is robust and highly active in aqueous media with very low overpotentials (30 mV). A variety of analytical techniques and electrochemical measurements suggest that the catalytically active sites are associated with the metal centres coordinated to nitrogen. This unusual atomic constitution of supported metals is suggestive of a new approach to preparing extremely efficient single-atom catalysts.

          Abstract

          There is ongoing interest in the development of non-precious metal catalysts for hydrogen evolution. Here, the authors fabricate a cobalt catalyst in which the cobalt is dispersed as single atoms on nitrogen-doped graphene, and report its high activity and stability for water reduction in acidic media.

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          Most cited references26

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          Water photolysis at 12.3% efficiency via perovskite photovoltaics and Earth-abundant catalysts.

          Although sunlight-driven water splitting is a promising route to sustainable hydrogen fuel production, widespread implementation is hampered by the expense of the necessary photovoltaic and photoelectrochemical apparatus. Here, we describe a highly efficient and low-cost water-splitting cell combining a state-of-the-art solution-processed perovskite tandem solar cell and a bifunctional Earth-abundant catalyst. The catalyst electrode, a NiFe layered double hydroxide, exhibits high activity toward both the oxygen and hydrogen evolution reactions in alkaline electrolyte. The combination of the two yields a water-splitting photocurrent density of around 10 milliamperes per square centimeter, corresponding to a solar-to-hydrogen efficiency of 12.3%. Currently, the perovskite instability limits the cell lifetime.
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            Nanoscale nickel oxide/nickel heterostructures for active hydrogen evolution electrocatalysis.

            Active, stable and cost-effective electrocatalysts are a key to water splitting for hydrogen production through electrolysis or photoelectrochemistry. Here we report nanoscale nickel oxide/nickel heterostructures formed on carbon nanotube sidewalls as highly effective electrocatalysts for hydrogen evolution reaction with activity similar to platinum. Partially reduced nickel interfaced with nickel oxide results from thermal decomposition of nickel hydroxide precursors bonded to carbon nanotube sidewalls. The metal ion-carbon nanotube interactions impede complete reduction and Ostwald ripening of nickel species into the less hydrogen evolution reaction active pure nickel phase. A water electrolyzer that achieves ~20 mA cm(-2) at a voltage of 1.5 V, and which may be operated by a single-cell alkaline battery, is fabricated using cheap, non-precious metal-based electrocatalysts.
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              Molybdenum phosphide as an efficient electrocatalyst for the hydrogen evolution reaction

              The phosphorization of molybdenum leads to a good non-noble metal catalyst for the hydrogen evolution reaction in both acidic and alkaline conditions.
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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Pub. Group
                2041-1723
                21 October 2015
                2015
                : 6
                : 8668
                Affiliations
                [1 ]Department of Chemistry, Rice University , 6100 Main Street, Houston, Texas 77005, USA
                [2 ]Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences , Beijing 100049, China
                [3 ]Department of Physics and Astronomy, University of Texas at San Antonio , One UTSA Circle, San Antonio, Texas 78249, USA
                [4 ]Department of Materials Science and NanoEngineering, Rice University , 6100 Main Street, Houston, Texas 77005, USA
                [5 ]Department of Electrical and Computer Engineering, University of Houston , Houston, Texas 77204, USA
                [6 ]Smalley Institute for Nanoscale Science and Technology, Rice University , 6100 Main Street, Houston, Texas 77005, USA
                Author notes
                Author information
                http://orcid.org/0000-0001-8860-093X
                http://orcid.org/0000-0002-8479-9328
                Article
                ncomms9668
                10.1038/ncomms9668
                4639894
                26487368
                d99c4146-3c35-4f5c-a517-9e97665c9562
                Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 23 June 2015
                : 17 September 2015
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