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      Handily etching nickel foams into catalyst–substrate fusion self‐stabilized electrodes toward industrial‐level water electrolysis

      1 , 1 , 1 , 2 , 1
      Carbon Energy
      Wiley

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          Abstract

          The key challenge of industrial water electrolysis is to design catalytic electrodes that can stabilize high current density with low power consumption (i.e., overpotential), while industrial harsh conditions make the balance between electrode activity and stability more difficult. Here, we develop an efficient and durable electrode for water oxidation reaction (WOR), which yields a high current density of 1000 mA cm −2 at an overpotential of only 284 mV in 1 M KOH at 25°C and shows robust stability even in 6 M KOH strong alkali with an elevated temperature up to 80°C. This electrode is fabricated from a cheap nickel foam (NF) substrate through a simple one‐step solution etching method, resulting in the growth of ultrafine phosphorus doped nickel‐iron (oxy)hydroxide [P‐(Ni,Fe)O x H y ] nanoparticles embedded into abundant micropores on the surface, featured as a self‐stabilized catalyst–substrate fusion electrode. Such self‐stabilizing effect fastens highly active P‐(Ni,Fe)O x H y species on conductive NF substrates with significant contribution to catalyst fixation and charge transfer, realizing a win–win tactics for WOR activity and durability at high current densities in harsh environments. This work affords a cost‐effective WOR electrode that can well work at large current densities, suggestive of the rational design of catalyst electrodes toward industrial‐scale water electrolysis.

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          Most cited references59

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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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            Nickel-iron oxyhydroxide oxygen-evolution electrocatalysts: the role of intentional and incidental iron incorporation.

            Fe plays a critical, but not yet understood, role in enhancing the activity of the Ni-based oxygen evolution reaction (OER) electrocatalysts. We report electrochemical, in situ electrical, photoelectron spectroscopy, and X-ray diffraction measurements on Ni(1-x)Fe(x)(OH)2/Ni(1-x)Fe(x)OOH thin films to investigate the changes in electronic properties, OER activity, and structure as a result of Fe inclusion. We developed a simple method for purification of KOH electrolyte that uses precipitated bulk Ni(OH)2 to absorb Fe impurities. Cyclic voltammetry on rigorously Fe-free Ni(OH)2/NiOOH reveals new Ni redox features and no significant OER current until >400 mV overpotential, different from previous reports which were likely affected by Fe impurities. We show through controlled crystallization that β-NiOOH is less active for OER than the disordered γ-NiOOH starting material and that previous reports of increased activity for β-NiOOH are due to incorporation of Fe-impurities during the crystallization process. Through-film in situ conductivity measurements show a >30-fold increase in film conductivity with Fe addition, but this change in conductivity is not sufficient to explain the observed changes in activity. Measurements of activity as a function of film thickness on Au and glassy carbon substrates are consistent with the hypothesis that Fe exerts a partial-charge-transfer activation effect on Ni, similar to that observed for noble-metal electrode surfaces. These results have significant implications for the design and study of Ni(1-x)Fe(x)OOH OER electrocatalysts, which are the fastest measured OER catalysts under basic conditions.
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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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                Author and article information

                Contributors
                Journal
                Carbon Energy
                Carbon Energy
                Wiley
                2637-9368
                2637-9368
                October 2023
                February 08 2023
                October 2023
                : 5
                : 10
                Affiliations
                [1 ] College of Physics Science and Technology, and Center for Interdisciplinary Research Yangzhou University Yangzhou People's Republic of China
                [2 ] Jiuchang New Energy Technology Co. Ltd. Yangzhou People's Republic of China
                Article
                10.1002/cey2.327
                80908eb0-f0ca-4b0b-a22e-dcf87608bbbb
                © 2023

                http://creativecommons.org/licenses/by/4.0/

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