{"title":"通过共掺杂调整 SnSe2 阳极的晶体优选取向,增强高性能钠存储的伪电容行为","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":"{\"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}","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
摘要
SnSe2 因其独特的二维层状结构而备受关注,与钠离子电池(SIB)的硬碳等传统负极材料相比,SnSe2 能够存储钠离子并具有更高的理论容量。然而,基于 SnSe2 的材料在离子存储过程中会因体积膨胀而导致结构损坏,从而导致循环稳定性和速率容量较差。在这项工作中,采用一步溶热法制备了具有优选晶体取向的掺杂 Co 的 SnSe2(Co-SnSe2)。研究发现,掺杂 Co 后,位于 14.4° 的较低 (001) 晶面取代了位于 30.7° 的较高 (101) 晶面,成为 Co-SnSe2 的主要晶面,从而显著促进了离子扩散并增强了伪电容行为。因此,这种 Co-SnSe2 阳极在 1 A g-1 条件下实现了 504 mAh g-1 的高容量,并具有高速循环稳定性,在 5 A g-1 条件下循环 1800 次后可实现 302 mAh g-1 的可逆容量,容量保持率高达 94%。此外,Na3V2(PO4)3||Co-SnSe2 全电池在 1 A g-1 下的稳定循环性能超过 300 次,显示出巨大的实际应用前景。这项工作为探索高性能储钠阳极材料提供了有效的参考。
Tuning Crystalline Preferred Orientation of SnSe2 Anode by Co-doping to Enhance Pseudocapacitive Behaviors for High-Performance Sodium Storage
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.