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      High-performance flexible supercapatteries enabled by binder-free two-dimensional mesoporous ultrathin nickel-ferrite nanosheets

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          Abstract

          To accomplish the efficient and high-performance supercapattery, electrochemically active materials with multi-component and rational morphological architectures are proposed.

          Abstract

          To accomplish an efficient and high-performance flexible supercapattery, electrochemically active materials with multicomponent and rational morphological architectures are highly enviable. Herein, we demonstrate dual-morphology-based mesoporous nickel-ferrite nanoparticles embedded in ultra-thin nanosheets (NiFe 2O 4-NP-NS) grown directly on a carbon cloth (CC) substrate to develop a free-standing electrode (NiFe 2O 4-NP-NS@CC) for a flexible supercapattery. Owing to the symmetric effects of bimetallic oxides, porosity with a higher surface area and dual morphological impact, the designed electrode conferred significantly enhanced electrochemical performance in aqueous as well as solid-state electrolytes. The binder-free architecture offered an excellent capacity of 965 C g -1 (1608 F g −1) at 5 mV s −1 with high coulombic efficiency and a good capacity retention of 94.20% over 5000 cycles, while the single morphology–based electrode showed only 551 C g −1 (919 F g −1) at 5 mV s −1 with a capacity retention of 90.50% over 5000 cycles under identical conditions. A redox-reaction mechanism is proposed based on ex situ XRD, XPS, and TEM analysis, and it further quantitatively distinguished the pseudocapacitive and diffusion-controlled charge storage proportions of NiFe 2O 4-NP-NS@CC cathodes in aqueous electrolytes. Additionally, the flexible supercapattery (NiFe 2O 4-NP-NS@CC//NPC) exhibits an outstanding energy density of 69 W h kg −1 at a power density of 771 W kg −1 with highly flexible features, which exceeds that of supercapacitors. These results present the fabricated device as a promising candidate in the field of energy storage.

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          Metallic Iron-Nickel Sulfide Ultrathin Nanosheets As a Highly Active Electrocatalyst for Hydrogen Evolution Reaction in Acidic Media.

          We report on the synthesis of iron-nickel sulfide (INS) ultrathin nanosheets by topotactic conversion from a hydroxide precursor. The INS nanosheets exhibit excellent activity and stability in strong acidic solutions as a hydrogen evolution reaction (HER) catalyst, lending an attractive alternative to the Pt catalyst. The metallic α-INS nanosheets show an even lower overpotential of 105 mV at 10 mA/cm(2) and a smaller Tafel slope of 40 mV/dec. With the help of DFT calculations, the high specific surface area, facile ion transport and charge transfer, abundant electrochemical active sites, suitable H(+) adsorption, and H2 formation kinetics and energetics are proposed to contribute to the high activity of the INS ultrathin nanosheets toward HER.
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            Silicon oxides: a promising family of anode materials for lithium-ion batteries

            Recent advances in the synthesis and lithium storage properties of silicon oxide-based anode materials. Silicon oxides have been recognized as a promising family of anode materials for high-energy lithium-ion batteries (LIBs) owing to their abundant reserve, low cost, environmental friendliness, easy synthesis, and high theoretical capacity. However, the extended application of silicon oxides is severely hampered by the intrinsically low conductivity, large volume change, and low initial coulombic efficiency. Significant efforts have been dedicated to tackling these challenges towards practical applications. This Review focuses on the recent advances in the synthesis and lithium storage properties of silicon oxide-based anode materials. To present the progress in a systematic manner, this review is categorized as follows: (i) SiO-based anode materials, (ii) SiO 2 -based anode materials, (iii) non-stoichiometric SiO x -based anode materials, and (iv) Si–O–C-based anode materials. Finally, future outlook and our personal perspectives on silicon oxide-based anode materials are presented.
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              Metal-organic framework-based materials for hybrid supercapacitor application

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                Author and article information

                Contributors
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                Journal
                MCFAC5
                Materials Chemistry Frontiers
                Mater. Chem. Front.
                Royal Society of Chemistry (RSC)
                2052-1537
                April 20 2021
                2021
                : 5
                : 8
                : 3436-3447
                Affiliations
                [1 ]Siyuan Laboratory
                [2 ]Guangdong Provincial Engineering Technology Research Center of Vacuum Coating Technologies and New Energy Materials
                [3 ]Department of Physics
                [4 ]Jinan University
                [5 ]Guangzhou 510632
                [6 ]Additive Manufacturing Institute, College of Mechatronics and Control Engineering, Shenzhen University
                [7 ]Shenzhen 518060
                [8 ]P. R. China
                [9 ]Institute of Microscale Optoelectronics, Shenzhen University
                [10 ]School of Material Science and Engineering
                [11 ]Xi’an Jiaotong University-Yulin University
                [12 ]Institute for Industrial Innovation of New Materials
                [13 ]Hefei National Laboratory for Physical Sciences at the Microscale
                [14 ]CAS Key Laboratory of Soft Matter Chemistry
                [15 ]School of Chemistry and Materials Science
                [16 ]University of Science and Technology of China
                [17 ]Hefei
                [18 ]Department of Chemistry
                [19 ]Faculty of Science
                [20 ]King Khalid University
                [21 ]Abha 61413
                [22 ]Saudi Arabia
                [23 ]College of Physics
                [24 ]Chongqing University
                [25 ]Chongqing 400044
                Article
                10.1039/D1QM00109D
                2b493f4a-6082-4df9-9765-4aa515635c3c
                © 2021

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

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