{"title":"三元硒化SnSb2Se4与石墨烯纳米片偶联用于高性能钾离子电池","authors":"Ruiqi Tian, Liping Duan, Yifan Xu, Yuehua Man, Jianlu Sun, Jianchun Bao, Xiaosi Zhou","doi":"10.1002/eem2.12617","DOIUrl":null,"url":null,"abstract":"<p>Although chalcogenide anodes possess higher potassium storage capacity than intercalated-based graphite, their drastic volume change and the irreversible electrochemical reactions still hinder the effective electron/ion transfer during the potassiation/depotassiation process. To solve the above problems, this article proposes the synthesis of a lamellar nanostructure where graphene nanosheets are embedded with SnSb<sub>2</sub>Se<sub>4</sub> nanoparticles (SnSb<sub>2</sub>Se<sub>4</sub>/GNS). In the product, fine monodisperse SnSb<sub>2</sub>Se<sub>4</sub> nanoparticles are coupled with graphene nanosheets to form a porous network framework, which can effectively mitigate the drastic volume changes during electrode reactions and guarantee efficient potassium-ion storage through the synergistic interactions among multiple elements. Various electrochemical analyses prove that SnSb<sub>2</sub>Se<sub>4</sub> inherits the advantages of the binary Sb<sub>2</sub>Se<sub>3</sub> and SnSe while avoiding their disadvantages, confirming the synergistic effect of the ternary–chalcogenide system. When tested for potassium storage, the obtained composite delivers a high specific capacity of 368.5 mAh g<sup>−1</sup> at 100 mA g<sup>−1</sup> and a stable cycle performance of 265.8 mAh g<sup>−1</sup> at 500 mA g<sup>−1</sup> over 500 cycles. Additionally, the potassium iron hexacyanoferrate cathode and the SnSb<sub>2</sub>Se<sub>4</sub>/GNS anode are paired to fabricate the potassium-ion full cell, which shows excellent cyclic stability. In conclusion, this strategy employs atomic doping and interface interaction, which provides new insights for the design of high-rate electrode materials.</p>","PeriodicalId":11554,"journal":{"name":"Energy & Environmental Materials","volume":"6 4","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2023-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eem2.12617","citationCount":"3","resultStr":"{\"title\":\"Coupling Ternary Selenide SnSb2Se4 with Graphene Nanosheets for High-Performance Potassium-Ion Batteries\",\"authors\":\"Ruiqi Tian, Liping Duan, Yifan Xu, Yuehua Man, Jianlu Sun, Jianchun Bao, Xiaosi Zhou\",\"doi\":\"10.1002/eem2.12617\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Although chalcogenide anodes possess higher potassium storage capacity than intercalated-based graphite, their drastic volume change and the irreversible electrochemical reactions still hinder the effective electron/ion transfer during the potassiation/depotassiation process. To solve the above problems, this article proposes the synthesis of a lamellar nanostructure where graphene nanosheets are embedded with SnSb<sub>2</sub>Se<sub>4</sub> nanoparticles (SnSb<sub>2</sub>Se<sub>4</sub>/GNS). In the product, fine monodisperse SnSb<sub>2</sub>Se<sub>4</sub> nanoparticles are coupled with graphene nanosheets to form a porous network framework, which can effectively mitigate the drastic volume changes during electrode reactions and guarantee efficient potassium-ion storage through the synergistic interactions among multiple elements. Various electrochemical analyses prove that SnSb<sub>2</sub>Se<sub>4</sub> inherits the advantages of the binary Sb<sub>2</sub>Se<sub>3</sub> and SnSe while avoiding their disadvantages, confirming the synergistic effect of the ternary–chalcogenide system. When tested for potassium storage, the obtained composite delivers a high specific capacity of 368.5 mAh g<sup>−1</sup> at 100 mA g<sup>−1</sup> and a stable cycle performance of 265.8 mAh g<sup>−1</sup> at 500 mA g<sup>−1</sup> over 500 cycles. Additionally, the potassium iron hexacyanoferrate cathode and the SnSb<sub>2</sub>Se<sub>4</sub>/GNS anode are paired to fabricate the potassium-ion full cell, which shows excellent cyclic stability. 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引用次数: 3
摘要
虽然硫族化物阳极比插层石墨具有更高的钾存储容量,但其剧烈的体积变化和不可逆的电化学反应仍然阻碍了钾化/脱钾过程中有效的电子/离子转移。为了解决上述问题,本文提出了在石墨烯纳米片上嵌入SnSb2Se4纳米粒子(SnSb2Se4/GNS)的层状纳米结构的合成方法。在该产品中,单分散的SnSb2Se4纳米颗粒与石墨烯纳米片耦合形成多孔网络框架,可以有效缓解电极反应过程中剧烈的体积变化,并通过多种元素之间的协同作用保证高效的钾离子储存。各种电化学分析证明SnSb2Se4继承了二元Sb2Se3和SnSe的优点,同时避免了它们的缺点,证实了三元硫族化合物体系的协同效应。当对钾储存进行测试时,所获得的复合材料在100 mA g - 1下提供368.5 mAh g - 1的高比容量,在500 mA g - 1下提供265.8 mAh g - 1的稳定循环性能,超过500次循环。此外,将六氰铁酸钾阴极与SnSb2Se4/GNS阳极配对,制备了具有良好循环稳定性的钾离子电池。总之,该策略采用了原子掺杂和界面相互作用,为高倍率电极材料的设计提供了新的见解。
Coupling Ternary Selenide SnSb2Se4 with Graphene Nanosheets for High-Performance Potassium-Ion Batteries
Although chalcogenide anodes possess higher potassium storage capacity than intercalated-based graphite, their drastic volume change and the irreversible electrochemical reactions still hinder the effective electron/ion transfer during the potassiation/depotassiation process. To solve the above problems, this article proposes the synthesis of a lamellar nanostructure where graphene nanosheets are embedded with SnSb2Se4 nanoparticles (SnSb2Se4/GNS). In the product, fine monodisperse SnSb2Se4 nanoparticles are coupled with graphene nanosheets to form a porous network framework, which can effectively mitigate the drastic volume changes during electrode reactions and guarantee efficient potassium-ion storage through the synergistic interactions among multiple elements. Various electrochemical analyses prove that SnSb2Se4 inherits the advantages of the binary Sb2Se3 and SnSe while avoiding their disadvantages, confirming the synergistic effect of the ternary–chalcogenide system. When tested for potassium storage, the obtained composite delivers a high specific capacity of 368.5 mAh g−1 at 100 mA g−1 and a stable cycle performance of 265.8 mAh g−1 at 500 mA g−1 over 500 cycles. Additionally, the potassium iron hexacyanoferrate cathode and the SnSb2Se4/GNS anode are paired to fabricate the potassium-ion full cell, which shows excellent cyclic stability. In conclusion, this strategy employs atomic doping and interface interaction, which provides new insights for the design of high-rate electrode materials.
期刊介绍:
Energy & Environmental Materials (EEM) is an international journal published by Zhengzhou University in collaboration with John Wiley & Sons, Inc. The journal aims to publish high quality research related to materials for energy harvesting, conversion, storage, and transport, as well as for creating a cleaner environment. EEM welcomes research work of significant general interest that has a high impact on society-relevant technological advances. The scope of the journal is intentionally broad, recognizing the complexity of issues and challenges related to energy and environmental materials. Therefore, interdisciplinary work across basic science and engineering disciplines is particularly encouraged. The areas covered by the journal include, but are not limited to, materials and composites for photovoltaics and photoelectrochemistry, bioprocessing, batteries, fuel cells, supercapacitors, clean air, and devices with multifunctionality. The readership of the journal includes chemical, physical, biological, materials, and environmental scientists and engineers from academia, industry, and policy-making.