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      An exquisite branch–leaf shaped metal sulfoselenide composite endowing an ultrastable sodium-storage lifespan over 10 000 cycles

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          Abstract

          An exquisite branch–leaf CNF@CoSSe@C was designed and fabricated, which favorably affords rich electrochemistry-active sites and multi-dimensional interconnected ion-transport channels, thus endowing superior sodium-storage lifespan over 13 000 cycles.

          Abstract

          Sluggish Na +-diffusion kinetics and inadequate ion-transport pathways in metal sulfides are one of the dominant bottlenecks for high-efficiency sodium-storage. Introducing hetero-anions into metal sulfides and further exploiting their advanced nanostructures is regarded as an innovative tactic. Herein, taking inspiration from biological systems, a three-dimensional hierarchical “branch–leaf” metal sulfoselenide anode, comprised of MOF-derived carbon-coated CoSSe nanoflake “leaves” and carbon nanofiber intertwined framework “branches” (CNF@CoSSe@C), was designed and fabricated through an electrospinning technique, impregnation growth and a subsequent series of high-temperature heat treatments, which favorably affords superior conductivity and mechanical strength, rich electrochemistry-active sites, multi-dimensional interconnected ion-transport channels, as well as short ion-diffusion distances. These significant advantages together with the exquisite structure are very conducive to highly effective sodium-storage, as attested by attractive specific capacity, impressive rate capability, and ultrastable cyclic lifespan over 13 000 cycles with a capacity fading rate of only 0.01% for every cycle at 20.0 A g −1. Further dissected by DFT calculations and scan-rate-dependent CV analysis, its superior sodium-storage features are mainly assigned to its significant surface-capacitive behavior and low energy barriers to Na + migration. The remarkable sodium-storage features stimulated us to set up a practical sodium-ion full-cell by matching it with an Na 3V 2(PO 4) 3@C cathode, showing a long-term cyclic lifespan of up to 1000 cycles at 3.0 A g −1 with a high reversible capacity of 156.3 mA h g −1.

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          Advances and Challenges in Metal Sulfides/Selenides for Next-Generation Rechargeable Sodium-Ion Batteries

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            Unique Cobalt Sulfide/Reduced Graphene Oxide Composite as an Anode for Sodium-Ion Batteries with Superior Rate Capability and Long Cycling Stability.

            Exploitation of high-performance anode materials is essential but challenging to the development of sodium-ion batteries (SIBs). Among all proposed anode materials for SIBs, sulfides have been proved promising candidates due to their unique chemical and physical properties. In this work, a facile solvothermal method to in situ decorate cobalt sulfide (CoS) nanoplates on reduced graphene oxide (rGO) to build CoS@rGO composite is described. When evaluated as anode for SIBs, an impressive high specific capacity (540 mAh g(-1) at 1 A g(-1) ), excellent rate capability (636 mAh g(-1) at 0.1 A g(-1) and 306 mAh g(-1) at 10 A g(-1)), and extraordinarily cycle stability (420 mAh g(-1) at 1 A g(-1) after 1000 cycles) have been demonstrated by CoS@rGO composite for sodium storage. The synergetic effect between the CoS nanoplates and rGO matrix contributes to the enhanced electrochemical performance of the hybrid composite. The results provide a facile approach to fabricate promising anode materials for high-performance SIBs.
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              Formation of Hierarchical Cu-Doped CoSe2 Microboxes via Sequential Ion Exchange for High-Performance Sodium-Ion Batteries

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                Author and article information

                Contributors
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                August 17 2022
                2022
                : 10
                : 32
                : 16962-16975
                Affiliations
                [1 ]School of Electronic Information Engineering, Yangtze Normal University, Fuling 408100, Chongqing, China
                [2 ]Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu 610054, Sichuan, China
                [3 ]National & Local Joint Engineering Research Center of Targeted and Innovative Therapeutics, College of Pharmacy, Chongqing University of Arts and Sciences, Yongchuan 402160, Chongqing, China
                [4 ]Institute for Advanced Study, Chengdu University, Chengdu 610106, Sichuan, China
                [5 ]Chemistry Department, Faculty of Science & Center of Excellence for Advanced Materials Research, King Abdulaziz University, P.O. Box 80203, Jeddah 21589, Saudi Arabia
                [6 ]College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan 250014, Shandong, China
                Article
                10.1039/D2TA05202D
                0f8eb609-7970-4d12-9433-e5e409073b90
                © 2022

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

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