{"title":"无阳极锂金属电池无缺陷锂沉积中的钾欠电位沉积。","authors":"Kassie Nigus Shitaw, Hailemariam Kassa Bezabh, Yosef Nikodimos, Misganaw Adigo Weret, Teshager Mekonnen Tekaligne, Semaw Kebede Merso, Bereket Woldegbreal Taklu, Shi-Kai Jiang, Chun-Ying Li, Hsin-Yueh Liu, She-Huang Wu, We-Nien Su, Bing Joe Hwang","doi":"10.1002/smtd.202500207","DOIUrl":null,"url":null,"abstract":"<p>Defects in deposited lithium (Li) severely cause dendrite growth and promote reactions between Li and electrolytes, resulting in active Li loss in anode-free Li metal batteries (AFLMBs). Herein, potassium underpotential deposition (K-UPD) is systematically established to heal defective Li and create a K-Cu bimetallic interface, facilitating uniform bulk Li deposition. The K-UPD at a potential of ≈1.0 V, higher than the equilibrium potentials of bulk K⁺ (0.1 V) and Li⁺ (0.0 V), significantly lowers the nucleation barrier and mitigates Li dendrite growth due to the better lithiophilicity of K metal compared to Cu. Meanwhile, the higher surface mobility of K atoms than Li atoms enables K metal to heal defects and prevent reactions between Li and electrolytes. The lower adsorption energy (ΔE) of the K atoms (−1.56 eV) than that of Li atoms (0.032 eV) indicates favorable adsorption of the K atom, as confirmed by DFT calculations. As a result, Cu||Li cell containing 1.3 M LiFSI+0.2 M KFSI bimetallic electrolyte reaches >1600 h, while Cu||NMC532 full-cell achieves a higher average Coulombic efficiency (avg. CE) of 99.6% than the cell with 1.5 M LiFSI electrolyte (≈98.2%) after the 100<sup>th</sup> cycle. This work offers insights into the K-UPD mechanism for enhancing interface stability and healing defects in deposited Li.</p>","PeriodicalId":229,"journal":{"name":"Small Methods","volume":"9 8","pages":""},"PeriodicalIF":9.1000,"publicationDate":"2025-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Potassium Underpotential Deposition for Defect-Free Lithium Deposition in Anode-Free Li-Metal Batteries\",\"authors\":\"Kassie Nigus Shitaw, Hailemariam Kassa Bezabh, Yosef Nikodimos, Misganaw Adigo Weret, Teshager Mekonnen Tekaligne, Semaw Kebede Merso, Bereket Woldegbreal Taklu, Shi-Kai Jiang, Chun-Ying Li, Hsin-Yueh Liu, She-Huang Wu, We-Nien Su, Bing Joe Hwang\",\"doi\":\"10.1002/smtd.202500207\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Defects in deposited lithium (Li) severely cause dendrite growth and promote reactions between Li and electrolytes, resulting in active Li loss in anode-free Li metal batteries (AFLMBs). Herein, potassium underpotential deposition (K-UPD) is systematically established to heal defective Li and create a K-Cu bimetallic interface, facilitating uniform bulk Li deposition. The K-UPD at a potential of ≈1.0 V, higher than the equilibrium potentials of bulk K⁺ (0.1 V) and Li⁺ (0.0 V), significantly lowers the nucleation barrier and mitigates Li dendrite growth due to the better lithiophilicity of K metal compared to Cu. Meanwhile, the higher surface mobility of K atoms than Li atoms enables K metal to heal defects and prevent reactions between Li and electrolytes. The lower adsorption energy (ΔE) of the K atoms (−1.56 eV) than that of Li atoms (0.032 eV) indicates favorable adsorption of the K atom, as confirmed by DFT calculations. As a result, Cu||Li cell containing 1.3 M LiFSI+0.2 M KFSI bimetallic electrolyte reaches >1600 h, while Cu||NMC532 full-cell achieves a higher average Coulombic efficiency (avg. CE) of 99.6% than the cell with 1.5 M LiFSI electrolyte (≈98.2%) after the 100<sup>th</sup> cycle. This work offers insights into the K-UPD mechanism for enhancing interface stability and healing defects in deposited Li.</p>\",\"PeriodicalId\":229,\"journal\":{\"name\":\"Small Methods\",\"volume\":\"9 8\",\"pages\":\"\"},\"PeriodicalIF\":9.1000,\"publicationDate\":\"2025-05-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Small Methods\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/smtd.202500207\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small Methods","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smtd.202500207","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
在无阳极锂金属电池(aflbs)中,沉积锂(Li)中的缺陷严重导致枝晶生长,并促进锂与电解质的反应,导致活性锂的损失。本文系统地建立了钾欠电位沉积(K-UPD)来修复缺陷的锂,并形成K-Cu双金属界面,促进均匀的大块锂沉积。K- upd电位≈1.0 V,高于体K + (0.1 V)和Li + (0.0 V)的平衡电位,由于K金属比Cu具有更好的亲锂性,K +显著降低了成核势垒,减缓了Li枝晶的生长。同时,K原子的表面迁移率比Li原子高,使得K金属能够修复缺陷,防止Li和电解质之间的反应。K原子的吸附能(ΔE) (-1.56 eV)比Li原子的吸附能(0.032 eV)低,表明K原子的吸附有利。结果表明,含1.3 M LiFSI+0.2 M KFSI双金属电解液的Cu||锂电池在第100次循环后达到>1600 h,而含1.5 M LiFSI电解液的Cu||NMC532全电池平均库仑效率(avg. CE)为99.6%,高于含1.5 M LiFSI电解液的电池(≈98.2%)。这项工作为K-UPD机制提高界面稳定性和修复沉积锂中的缺陷提供了新的见解。
Potassium Underpotential Deposition for Defect-Free Lithium Deposition in Anode-Free Li-Metal Batteries
Defects in deposited lithium (Li) severely cause dendrite growth and promote reactions between Li and electrolytes, resulting in active Li loss in anode-free Li metal batteries (AFLMBs). Herein, potassium underpotential deposition (K-UPD) is systematically established to heal defective Li and create a K-Cu bimetallic interface, facilitating uniform bulk Li deposition. The K-UPD at a potential of ≈1.0 V, higher than the equilibrium potentials of bulk K⁺ (0.1 V) and Li⁺ (0.0 V), significantly lowers the nucleation barrier and mitigates Li dendrite growth due to the better lithiophilicity of K metal compared to Cu. Meanwhile, the higher surface mobility of K atoms than Li atoms enables K metal to heal defects and prevent reactions between Li and electrolytes. The lower adsorption energy (ΔE) of the K atoms (−1.56 eV) than that of Li atoms (0.032 eV) indicates favorable adsorption of the K atom, as confirmed by DFT calculations. As a result, Cu||Li cell containing 1.3 M LiFSI+0.2 M KFSI bimetallic electrolyte reaches >1600 h, while Cu||NMC532 full-cell achieves a higher average Coulombic efficiency (avg. CE) of 99.6% than the cell with 1.5 M LiFSI electrolyte (≈98.2%) after the 100th cycle. This work offers insights into the K-UPD mechanism for enhancing interface stability and healing defects in deposited Li.
Small MethodsMaterials Science-General Materials Science
CiteScore
17.40
自引率
1.60%
发文量
347
期刊介绍:
Small Methods is a multidisciplinary journal that publishes groundbreaking research on methods relevant to nano- and microscale research. It welcomes contributions from the fields of materials science, biomedical science, chemistry, and physics, showcasing the latest advancements in experimental techniques.
With a notable 2022 Impact Factor of 12.4 (Journal Citation Reports, Clarivate Analytics, 2023), Small Methods is recognized for its significant impact on the scientific community.
The online ISSN for Small Methods is 2366-9608.