{"title":"Edge Electron Effect Induced High-Entropy SEI for Durable Anode-Free Sodium Batteries","authors":"Junmin Ge, Cunshuang Ma, Yaoyang Zhang, Pei Ma, Jiyu Zhang, Zhengkun Xie, Longfei Wen, Guochuan Tang, Qingbao Wang, Wenbin Li, Xiaoniu Guo, Ying Guo, Erjin Zhang, YongChao Zhang, Lingfei Zhao, Weihua Chen","doi":"10.1002/adma.202413253","DOIUrl":null,"url":null,"abstract":"Anode-free sodium metal batteries represent great promising as high-energy-density and resource-rich electrochemical energy storage systems. However, the savage growth of sodium metal and continuous consumption hinder its stable capacity output. Herein, ordered flower-edges of zinc on Al substrate can induce high-entropy solid electrolyte interphase (SEI) to adjust sodium uniform deposition and extremely reduce electrolyte consumption with ultrahigh initial Coulombic efficiency (97.05%) for prolong batteries cycling life. Theoretical and experimental studies have demonstrated that the electron-donating property and exposed edge sites between (100) and (101) facets in zinc flower enhance anion adsorption onto the inner Helmholtz plane accelerating its interface decomposition. Additionally, the ordered zinc edges serve as homogeneous-nucleating template, leading to thin and inorganic-rich SEI layer (18 nm, ZnF<sub>2</sub>, NaZn<sub>13</sub>, NaF, and Na<sub>2</sub>CO<sub>3</sub>) with high-entropy discrete multicomponent distribution, so that fast and high-flux Na ions transport field, thereby reducing the critical nucleation barrier and promoting sodium high density nucleation (7.36 × 10<sup>13</sup> N cm<sup>−2</sup>) and pyknotic growth (3 mAh cm<sup>−2</sup>, 22 µm). The assembled anode-free sodium batteries exhibit high stability (86%, 90 cycles) under ultrahigh cathode loading (32 mg cm<sup>−2</sup>). Moreover, the anode-less single-layer pouch batteries exhibit a durable capacity retention of 99% after 600 cycles.","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":"2 1","pages":""},"PeriodicalIF":27.4000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adma.202413253","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Anode-free sodium metal batteries represent great promising as high-energy-density and resource-rich electrochemical energy storage systems. However, the savage growth of sodium metal and continuous consumption hinder its stable capacity output. Herein, ordered flower-edges of zinc on Al substrate can induce high-entropy solid electrolyte interphase (SEI) to adjust sodium uniform deposition and extremely reduce electrolyte consumption with ultrahigh initial Coulombic efficiency (97.05%) for prolong batteries cycling life. Theoretical and experimental studies have demonstrated that the electron-donating property and exposed edge sites between (100) and (101) facets in zinc flower enhance anion adsorption onto the inner Helmholtz plane accelerating its interface decomposition. Additionally, the ordered zinc edges serve as homogeneous-nucleating template, leading to thin and inorganic-rich SEI layer (18 nm, ZnF2, NaZn13, NaF, and Na2CO3) with high-entropy discrete multicomponent distribution, so that fast and high-flux Na ions transport field, thereby reducing the critical nucleation barrier and promoting sodium high density nucleation (7.36 × 1013 N cm−2) and pyknotic growth (3 mAh cm−2, 22 µm). The assembled anode-free sodium batteries exhibit high stability (86%, 90 cycles) under ultrahigh cathode loading (32 mg cm−2). Moreover, the anode-less single-layer pouch batteries exhibit a durable capacity retention of 99% after 600 cycles.
无阳极金属钠电池作为高能量密度和资源丰富的电化学储能系统,具有广阔的发展前景。然而,金属钠的野蛮生长和持续消耗阻碍了其稳定的容量输出。在此,铝基底上有序的花边锌可以诱导高熵固态电解质相间(SEI),从而调节钠的均匀沉积,极大地减少电解质的消耗,并以超高的初始库仑效率(97.05%)延长电池的循环寿命。理论和实验研究表明,锌花中(100)和(101)面之间的电子负载特性和暴露的边缘位点增强了内赫尔姆霍兹平面上的阴离子吸附,加速了其界面分解。此外,有序的锌边可作为均匀成核模板,形成薄而富含无机物的 SEI 层(18 nm,ZnF2、NaZn13、NaF 和 Na2CO3),具有高熵离散多组分分布,从而使 Na 离子快速、高通量地传输场,从而降低临界成核障碍,促进钠的高密度成核(7.36 × 1013 N cm-2)和热结生长(3 mAh cm-2,22 µm)。组装好的无阳极钠电池在超高阴极负载(32 毫克厘米-2)条件下表现出很高的稳定性(86%,90 次循环)。此外,无阳极单层袋式电池在 600 次循环后的容量保持率高达 99%。
期刊介绍:
Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.