{"title":"Tuning Crystalline Preferred Orientation of SnSe2 Anode by Co-doping to Enhance Pseudocapacitive Behaviors for High-Performance Sodium Storage","authors":"Dejian Liu, Jiarui Zhong, Zhiyi Cai, Zijian Zhan, Cheng Zheng, Shaoming Huang","doi":"10.1021/acsami.4c13110","DOIUrl":null,"url":null,"abstract":"SnSe<sub>2</sub> has attracted great attention due to its unique 2D-layered structure, which makes it capable of sodium ion storage and higher theoretical capacities compared to traditional anode materials like hard carbon for sodium ion batteries (SIBs). However, SnSe<sub>2</sub>-based materials will cause structural damage due to volume expansion during ion storage, leading to poor cycle stability and rate capacity. In this work, Co-doped SnSe<sub>2</sub> (Co-SnSe<sub>2</sub>) with preferred crystal orientation was fabricated by a one-step solvothermal method. It has been found that after doping Co, the lower (001) crystal plane located at 14.4° replaced the higher (101) plane at 30.7° as the dominant crystal plane in Co-SnSe<sub>2</sub>, which significantly promoted ion diffusion and enhanced the pseudocapacitance behavior. Therefore, this Co-SnSe<sub>2</sub> anode achieves a high capacity of 504 mAh g<sup>–1</sup> at 1 A g<sup>–1</sup>, and a high-rate cycle stability, delivering a reversible capacity of 302 mAh g<sup>–1</sup> at 5 A g<sup>–1</sup> after 1800 cycles with a retained capacity rate of 94%. Moreover, the Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub>||Co-SnSe<sub>2</sub> full cell exhibits a stable cycle performance of over 300 cycles at 1 A g<sup>–1</sup>, demonstrating great promise for practical applications. This work provides an effective reference for the exploration of high-performance sodium storage anode materials.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"55 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2024-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsami.4c13110","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
SnSe2 has attracted great attention due to its unique 2D-layered structure, which makes it capable of sodium ion storage and higher theoretical capacities compared to traditional anode materials like hard carbon for sodium ion batteries (SIBs). However, SnSe2-based materials will cause structural damage due to volume expansion during ion storage, leading to poor cycle stability and rate capacity. In this work, Co-doped SnSe2 (Co-SnSe2) with preferred crystal orientation was fabricated by a one-step solvothermal method. It has been found that after doping Co, the lower (001) crystal plane located at 14.4° replaced the higher (101) plane at 30.7° as the dominant crystal plane in Co-SnSe2, which significantly promoted ion diffusion and enhanced the pseudocapacitance behavior. Therefore, this Co-SnSe2 anode achieves a high capacity of 504 mAh g–1 at 1 A g–1, and a high-rate cycle stability, delivering a reversible capacity of 302 mAh g–1 at 5 A g–1 after 1800 cycles with a retained capacity rate of 94%. Moreover, the Na3V2(PO4)3||Co-SnSe2 full cell exhibits a stable cycle performance of over 300 cycles at 1 A g–1, demonstrating great promise for practical applications. This work provides an effective reference for the exploration of high-performance sodium storage anode materials.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.