{"title":"Boosting the initial Coulombic efficiency of Bi2S3-based anode for practical sodium-ion batteries","authors":"Lankun Shi, Rongji Jiao, Dawei Lan, Li Wang, Yu Gao, Meng-Fang Lin, Zhongmin Lang, Wenxiu He, Guixiao Jia, Jinlong Cui, Shaohui Li","doi":"10.1016/j.cej.2025.165074","DOIUrl":null,"url":null,"abstract":"Bi<sub>2</sub>S<sub>3</sub> is a promising anode candidate for sodium-ion batteries (SIBs) due to its high capacity and cost-effectiveness. However, the severe volume expansion that occurs during sodiation/desodiation processes results in inferior cycling stability and low initial Coulombic efficiency (ICE), which hinders its further development. Herein, we deposited Bi<sub>2</sub>S<sub>3</sub> nanorods onto lignite-derived carbon skeleton (Bi<sub>2</sub>S<sub>3</sub>/LC) via a solvothermal method for high performance anode. Experimental studies combined with theoretical calculation reveal that the presence of LC can enhance the porosity and sulfur vacancies of Bi<sub>2</sub>S<sub>3</sub>, boost the adsorption ability and reversibility of its sodiation intermediate NaBiS<sub>2</sub> for Na<sup>+</sup>. Additionally, incorporating fluoroethylene carbonate (FEC) into the ester-based electrolyte enables the in-situ formation of a conformal and ultra-thin NaF-rich solid electrolyte interphase (SEI) on the anode surface and improves its structural stability. These advancements endow Bi<sub>2</sub>S<sub>3</sub>/LC anode displays an excellent ICE (up to 93.2% at 0.1 A g<sup>−1</sup>), rapid sodium storage capability (388.8 mAh g<sup>−1</sup> at 8 A g<sup>−1</sup>), and impressive cycle stability (up to 96.3% capacity retention after 1000 cycles at 10 A g<sup>−1</sup>). The exceptional Na<sup>+</sup> storage capability of Bi<sub>2</sub>S<sub>3</sub>/LC anode also enables the assemable SIB full cell to demonstrate impressive rate capability and cycling stability, underscoring their potential for high-performance practical applications.","PeriodicalId":270,"journal":{"name":"Chemical Engineering Journal","volume":"91 1","pages":""},"PeriodicalIF":13.2000,"publicationDate":"2025-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.cej.2025.165074","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Bi2S3 is a promising anode candidate for sodium-ion batteries (SIBs) due to its high capacity and cost-effectiveness. However, the severe volume expansion that occurs during sodiation/desodiation processes results in inferior cycling stability and low initial Coulombic efficiency (ICE), which hinders its further development. Herein, we deposited Bi2S3 nanorods onto lignite-derived carbon skeleton (Bi2S3/LC) via a solvothermal method for high performance anode. Experimental studies combined with theoretical calculation reveal that the presence of LC can enhance the porosity and sulfur vacancies of Bi2S3, boost the adsorption ability and reversibility of its sodiation intermediate NaBiS2 for Na+. Additionally, incorporating fluoroethylene carbonate (FEC) into the ester-based electrolyte enables the in-situ formation of a conformal and ultra-thin NaF-rich solid electrolyte interphase (SEI) on the anode surface and improves its structural stability. These advancements endow Bi2S3/LC anode displays an excellent ICE (up to 93.2% at 0.1 A g−1), rapid sodium storage capability (388.8 mAh g−1 at 8 A g−1), and impressive cycle stability (up to 96.3% capacity retention after 1000 cycles at 10 A g−1). The exceptional Na+ storage capability of Bi2S3/LC anode also enables the assemable SIB full cell to demonstrate impressive rate capability and cycling stability, underscoring their potential for high-performance practical applications.
由于其高容量和成本效益,Bi2S3是一种很有前途的钠离子电池(sib)阳极候选材料。然而,在钠化/脱钠过程中发生的严重体积膨胀导致循环稳定性差,初始库仑效率(ICE)较低,阻碍了其进一步发展。在此,我们通过溶剂热法将Bi2S3纳米棒沉积在褐煤衍生的碳骨架(Bi2S3/LC)上作为高性能阳极。实验研究结合理论计算表明,LC的存在增强了Bi2S3的孔隙度和硫空位,提高了其中介体NaBiS2对Na+的吸附能力和可逆性。此外,将氟碳酸乙烯(FEC)加入到酯基电解质中,可以在阳极表面原位形成适形的超薄富钠固体电解质界面(SEI),并提高其结构稳定性。这些进步使Bi2S3/LC阳极显示出优异的ICE(在0.1 A g−1时高达93.2%),快速的钠存储能力(在8 A g−1时388.8 mAh g−1),以及令人印象深刻的循环稳定性(在10 A g−1下1000次 循环后高达96.3%的容量保留)。Bi2S3/LC阳极卓越的Na+存储能力也使可组装的SIB全电池表现出令人印象深刻的速率能力和循环稳定性,强调了它们在高性能实际应用中的潜力。
期刊介绍:
The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.