Xuzi Zhang , Jialiang Wang , Hanlin Wang , Han Huang , Hao Zhang , Ge Li
{"title":"Unlocking dendrite-free zinc metal anodes through anti-corrosive and Zn-ion-regulating interlayer","authors":"Xuzi Zhang , Jialiang Wang , Hanlin Wang , Han Huang , Hao Zhang , Ge Li","doi":"10.1016/j.nxener.2024.100124","DOIUrl":null,"url":null,"abstract":"<div><p>Aqueous zinc-ion batteries (AZIBs) are a promising solution for large-scale energy storage due to their safety and cost-effectiveness. However, challenges like zinc dendrite growth and electrolyte corrosion hinder their practical use. Surface engineering methods have shown potential in stabilizing the zinc metal anode interface. In this study, we propose a successful approach by combining 2D g-C<sub>3</sub>N<sub>4</sub> nanosheets with 3D ZIF8 nanoparticles to form a g-C<sub>3</sub>N<sub>4</sub>@ZIF8 artificial interface. The 3D ZIF8 support on the 2D g-C<sub>3</sub>N<sub>4</sub> enables precise regulation of Zn<sup>2+</sup> flux and efficient charge transfer, leading to improved electrochemical performance. Density functional theory confirms ZIF8's superior adsorption energy compared to g-C<sub>3</sub>N<sub>4</sub>. Strategically anchoring 3D ZIF8 nanoparticles within 2D g-C<sub>3</sub>N<sub>4</sub> allows robust 3D diffusion of Zn<sup>2+</sup>, preventing dendrite formation and enabling dendrite-free Zn deposition. This structural design can enhance the performance of symmetric cells with an ultralong cycling lifespan of up to 6200 h at 0.25 mA cm<sup>−2</sup>/0.25 mA h cm<sup>−2</sup> and superior rate capability, even at 40 mA cm<sup>−2</sup>. When combined with a V<sub>2</sub>O<sub>5</sub> nanopaper cathode, our assembled AZIBs exhibit stable long-term performance. This research paves the way for more efficient and reliable AZIBs for large-scale energy storage.</p></div>","PeriodicalId":100957,"journal":{"name":"Next Energy","volume":"4 ","pages":"Article 100124"},"PeriodicalIF":0.0000,"publicationDate":"2024-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949821X24000292/pdfft?md5=76179bbf082890d62d5029bbc4e0e21a&pid=1-s2.0-S2949821X24000292-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Next Energy","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949821X24000292","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Aqueous zinc-ion batteries (AZIBs) are a promising solution for large-scale energy storage due to their safety and cost-effectiveness. However, challenges like zinc dendrite growth and electrolyte corrosion hinder their practical use. Surface engineering methods have shown potential in stabilizing the zinc metal anode interface. In this study, we propose a successful approach by combining 2D g-C3N4 nanosheets with 3D ZIF8 nanoparticles to form a g-C3N4@ZIF8 artificial interface. The 3D ZIF8 support on the 2D g-C3N4 enables precise regulation of Zn2+ flux and efficient charge transfer, leading to improved electrochemical performance. Density functional theory confirms ZIF8's superior adsorption energy compared to g-C3N4. Strategically anchoring 3D ZIF8 nanoparticles within 2D g-C3N4 allows robust 3D diffusion of Zn2+, preventing dendrite formation and enabling dendrite-free Zn deposition. This structural design can enhance the performance of symmetric cells with an ultralong cycling lifespan of up to 6200 h at 0.25 mA cm−2/0.25 mA h cm−2 and superior rate capability, even at 40 mA cm−2. When combined with a V2O5 nanopaper cathode, our assembled AZIBs exhibit stable long-term performance. This research paves the way for more efficient and reliable AZIBs for large-scale energy storage.