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      Industrially promising NiCoP nanorod arrays tailored with trace W and Mo atoms for boosting large-current-density overall water splitting

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          Abstract

          Using the classic NiCoP nanorod arrays as the basic catalyst model, we presented a trace W and Mo co-doped strategy to boost the overall water splitting electrocatalysis at an industrial current density.

          Abstract

          Nanoarray catalysts supported on substrates provide an opportunity for industrially promising overall water splitting at large current densities. However, most of the present electrocatalysts show high overpotentials at a large current density, inducing a low efficiency for industrial water electrolysis. Herein, using the classic NiCoP nanorod arrays as the basic catalyst model, we presented a trace W and Mo co-doped strategy to boost the overall water splitting electrocatalysis at an industrial current density. After a trace amount of W and Mo atoms was doped, the constructed W and Mo co-doped NiCoP nanorod arrays (W,Mo-NiCoP/NF) show a low overpotential of 249 mV towards the hydrogen evolution reaction (HER) at a very large current density of 1000 mA cm −2. We deduce that the regulation of the electronic structure caused by the trace W and Mo atoms, as well as the intrinsic features of nanoarrays leads to enhanced catalytic activity. In addition, a significant enhancement towards the oxygen evolution reaction (OER) was also achieved by this co-doped strategy. Finally, an overall water splitting device using W,Mo-NiCoP/NF as both the anode and cathode was assembled to exhibit a low cell voltage of 1.85 V at a large current density of 500 mA cm −2 and an excellent long-term stability within 50 h, better than most of the state-of-the-art bifunctional electrocatalysts yet reported. Our results highlight the significance of trace-doping engineering in industrial water electrolysis.

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          Most cited references67

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          What would it take for renewably powered electrosynthesis to displace petrochemical processes?

          Electrocatalytic transformation of carbon dioxide (CO 2 ) and water into chemical feedstocks offers the potential to reduce carbon emissions by shifting the chemical industry away from fossil fuel dependence. We provide a technoeconomic and carbon emission analysis of possible products, offering targets that would need to be met for economically compelling industrial implementation to be achieved. We also provide a comparison of the projected costs and CO 2 emissions across electrocatalytic, biocatalytic, and fossil fuel–derived production of chemical feedstocks. We find that for electrosynthesis to become competitive with fossil fuel–derived feedstocks, electrical-to-chemical conversion efficiencies need to reach at least 60%, and renewable electricity prices need to fall below 4 cents per kilowatt-hour. We discuss the possibility of combining electro- and biocatalytic processes, using sequential upgrading of CO 2 as a representative case. We describe the technical challenges and economic barriers to marketable electrosynthesized chemicals.
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            Innovative Strategies for Electrocatalytic Water Splitting

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              From hydrogenases to noble metal-free catalytic nanomaterials for H2 production and uptake.

              Interconversion of water and hydrogen in unitized regenerative fuel cells is a promising energy storage framework for smoothing out the temporal fluctuations of solar and wind power. However, replacement of presently available platinum catalysts by lower-cost and more abundant materials is a requisite for this technology to become economically viable. Here, we show that the covalent attachment of a nickel bisdiphosphine-based mimic of the active site of hydrogenase enzymes onto multiwalled carbon nanotubes results in a high-surface area cathode material with high catalytic activity under the strongly acidic conditions required in proton exchange membrane technology. Hydrogen evolves from aqueous sulfuric acid solution with very low overvoltages (20 millivolts), and the catalyst exhibits exceptional stability (more than 100,000 turnovers). The same catalyst is also very efficient for hydrogen oxidation in this environment, exhibiting current densities similar to those observed for hydrogenase-based materials.
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                Author and article information

                Contributors
                Journal
                NANOHL
                Nanoscale
                Nanoscale
                Royal Society of Chemistry (RSC)
                2040-3364
                2040-3372
                August 26 2021
                2021
                : 13
                : 33
                : 14179-14185
                Affiliations
                [1 ]MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, Heilongjiang 150001, China
                Article
                10.1039/D1NR03186D
                92501d4f-ddfc-4e34-8091-7217e3f76ab3
                © 2021

                http://rsc.li/journals-terms-of-use

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