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      Ti 3C 2 mediates the NiFe-LDH layered electrocatalyst to enhance the OER performance for water splitting

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          Abstract

          Oxygen evolution reaction (OER) is a very complex process with slow reaction kinetics and high overpotential, which is the main limitation for the commercial application of water splitting. Thus, it is of necessary to design high-performance OER catalysts. NiFe based layered double hydroxides (NiFe-LDHs) have recently gained a lot of attention due to their high reaction activity and simple manufacturing process. In this study, a novel electrocatalyst based on NiFe-LDH was constructed by introducing Ti 3C 2, which was utilized to modulate the structural and electronic properties of the electrocatalysts. Structural examinations reveal that the Ti 3C 2 of 2D structure successfully dope the NiFe-LDHs nanosheets, forming NiFe-LDH/Ti 3C 2 heterojunctions. Firstly, the heterojunction substantially reduces the charge transfer resistance, promoting the electron migration between the LDH nanosheets. Secondly, theoretical calculations demonstrate that the energy barrier between the rate-determining step from *OH to *O is lowered, favoring the formation of the reaction intermediates and thus the occurrence of OER. As a result, the composite electrocatalyst exhibits a low overpotential of 334 mV at a current density of 10 mA/cm 2 and a small Tafel slope of 55 mV/dec, which are superior to those of the NiFe-LDH by 11.2 % and 38.5 %, respectively. This study provides inspiration for promoting the performances of NiFe based electrocatalysts by utilizing 2D materials.

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          Most cited references34

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          Combining theory and experiment in electrocatalysis: Insights into materials design

          Electrocatalysis plays a central role in clean energy conversion, enabling a number of sustainable processes for future technologies. This review discusses design strategies for state-of-the-art heterogeneous electrocatalysts and associated materials for several different electrochemical transformations involving water, hydrogen, and oxygen, using theory as a means to rationalize catalyst performance. By examining the common principles that govern catalysis for different electrochemical reactions, we describe a systematic framework that clarifies trends in catalyzing these reactions, serving as a guide to new catalyst development while highlighting key gaps that need to be addressed. We conclude by extending this framework to emerging clean energy reactions such as hydrogen peroxide production, carbon dioxide reduction, and nitrogen reduction, where the development of improved catalysts could allow for the sustainable production of a broad range of fuels and chemicals.
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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.
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              An advanced Ni-Fe layered double hydroxide electrocatalyst for water oxidation.

              Highly active, durable, and cost-effective electrocatalysts for water oxidation to evolve oxygen gas hold a key to a range of renewable energy solutions, including water-splitting and rechargeable metal-air batteries. Here, we report the synthesis of ultrathin nickel-iron layered double hydroxide (NiFe-LDH) nanoplates on mildly oxidized multiwalled carbon nanotubes (CNTs). Incorporation of Fe into the nickel hydroxide induced the formation of NiFe-LDH. The crystalline NiFe-LDH phase in nanoplate form is found to be highly active for oxygen evolution reaction in alkaline solutions. For NiFe-LDH grown on a network of CNTs, the resulting NiFe-LDH/CNT complex exhibits higher electrocatalytic activity and stability for oxygen evolution than commercial precious metal Ir catalysts.
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                Author and article information

                Contributors
                Journal
                Heliyon
                Heliyon
                Heliyon
                Elsevier
                2405-8440
                14 May 2024
                30 May 2024
                14 May 2024
                : 10
                : 10
                : e30966
                Affiliations
                [a ]Key Laboratory of Plateau Oxygen and Living Environment of Tibet Autonomous Region, College of Science, Tibet University, Lhasa, 850000, China
                [b ]College of Information Engineering, Xizang Minzu University, Xianyang 712000, China
                Author notes
                [* ]Corresponding author. wsf@ 123456utibet.edu.cn
                [** ]Corresponding author. bding@ 123456xzmu.edu.cn
                [1]

                These authors contributed equally.

                Article
                S2405-8440(24)06997-4 e30966
                10.1016/j.heliyon.2024.e30966
                11112313
                38784544
                757c712e-09fc-4e77-8c14-f35a5137a356
                © 2024 The Authors. Published by Elsevier Ltd.

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 20 March 2024
                : 30 April 2024
                : 8 May 2024
                Categories
                Research Article

                layered double hydroxides,oer,electrocatalyst,ti3c2,2d materials

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