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      Well-defined hierarchical teddy bear sunflower-like NiCo 2O 4 electrocatalyst for superior water oxidation

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          Abstract

          Transition metal oxides were fabricated by a facile solvothermal route. The hierarchical NiCo 2O 4 electrocatalyst exhibited enhanced water oxidation performance due to the unique teddy bear sunflower-like morphology.

          Abstract

          The development of a robust and efficient electrocatalyst for water oxidation is challenging due to the large overpotential requirement to transfer four electrons. Herein, a novel spinel-type hierarchical teddy bear sunflower-like NiCo 2O 4 electrocatalyst was synthesized through the facile solvothermal process and evaluated for the challenging and demanding oxygen evolution reaction (OER) in the water electrolysis process. The teddy bear sunflower-like NiCo 2O 4 supported on nickel foam (NF) delivers a current density of 50 mA cm −2 at a small water oxidation overpotential ( η 50 = 319 mV) which is significantly lower than that of the corresponding spherical NiO/NF ( η 50 = 338 mV), and sea-urchin like Co 3O 4/NF ( η 50 = 357 mV). A large specific and electroactive surface area, as well as a high TOF value exhibited by the hierarchical teddy bear sunflower-like NiCo 2O 4 electrocatalyst, demonstrates the potential of NiCo 2O 4 to catalyze the water oxidation reaction efficiently. The impact of the near-Fermi-level d-orbital states in NiCo 2O 4 electrocatalyst for boosting OER activity was unveiled by the density functional theory calculation. The stable performance even after 16 h and high catalyst utilization of the hierarchical teddy bear sunflower-like NiCo 2O 4 through the OER indicates that the catalyst is highly suitable for the large-scale water oxidation process.

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          Electron-energy-loss spectra and the structural stability of nickel oxide: An LSDA+U study

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            Opportunities and challenges for a sustainable energy future.

            Access to clean, affordable and reliable energy has been a cornerstone of the world's increasing prosperity and economic growth since the beginning of the industrial revolution. Our use of energy in the twenty-first century must also be sustainable. Solar and water-based energy generation, and engineering of microbes to produce biofuels are a few examples of the alternatives. This Perspective puts these opportunities into a larger context by relating them to a number of aspects in the transportation and electricity generation sectors. It also provides a snapshot of the current energy landscape and discusses several research and development opportunities and pathways that could lead to a prosperous, sustainable and secure energy future for the world.
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              Benchmarking heterogeneous electrocatalysts for the oxygen evolution reaction.

              Objective evaluation of the activity of electrocatalysts for water oxidation is of fundamental importance for the development of promising energy conversion technologies including integrated solar water-splitting devices, water electrolyzers, and Li-air batteries. However, current methods employed to evaluate oxygen-evolving catalysts are not standardized, making it difficult to compare the activity and stability of these materials. We report a protocol for evaluating the activity, stability, and Faradaic efficiency of electrodeposited oxygen-evolving electrocatalysts. In particular, we focus on methods for determining electrochemically active surface area and measuring electrocatalytic activity and stability under conditions relevant to an integrated solar water-splitting device. Our primary figure of merit is the overpotential required to achieve a current density of 10 mA cm(-2) per geometric area, approximately the current density expected for a 10% efficient solar-to-fuels conversion device. Utilizing the aforementioned surface area measurements, one can determine electrocatalyst turnover frequencies. The reported protocol was used to examine the oxygen-evolution activity of the following systems in acidic and alkaline solutions: CoO(x), CoPi, CoFeO(x), NiO(x), NiCeO(x), NiCoO(x), NiCuO(x), NiFeO(x), and NiLaO(x). The oxygen-evolving activity of an electrodeposited IrO(x) catalyst was also investigated for comparison. Two general observations are made from comparing the catalytic performance of the OER catalysts investigated: (1) in alkaline solution, every non-noble metal system achieved 10 mA cm(-2) current densities at similar operating overpotentials between 0.35 and 0.43 V, and (2) every system but IrO(x) was unstable under oxidative conditions in acidic solutions.

                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                SEFUA7
                Sustainable Energy & Fuels
                Sustainable Energy Fuels
                Royal Society of Chemistry (RSC)
                2398-4902
                December 06 2022
                2022
                : 6
                : 24
                : 5491-5502
                Affiliations
                [1 ]National Centre for Nanosciences and Nanotechnology, University of Mumbai, Kalina, Mumbai-400098, India
                [2 ]Department of Physics, University of Mumbai, Kalina, Mumbai-400098, India
                [3 ]CSIRO Energy, Private Bag 10, Clayton South 319, Victoria, Australia
                [4 ]Academy of Scientific and Innovative Research, CSIR-Human Resource Development Center (CSIR-HRDC) Campus, Postal Staff College Area, Ghaziabad, Uttar Pradesh, 201002, India
                [5 ]Electronic Structure Theory Group, Physical and Materials Chemistry Division, CSIR-National Chemical Laboratory, Pune, 411008, India
                Article
                10.1039/D2SE01111E
                af63ffc5-fc8f-40e7-94db-50f2e0e3224e
                © 2022

                http://creativecommons.org/licenses/by-nc/3.0/

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