Qianhui Zhang, Yingxin Zhang, Lanzhi Ke, Haonan Jiang, Yuan Huang, Zanxiang Nie, Shunyu Jin
{"title":"Biocompatible hydrogel electrolyte with high ionic conductivity and transference number towards dendrite-free Zn anodes","authors":"Qianhui Zhang, Yingxin Zhang, Lanzhi Ke, Haonan Jiang, Yuan Huang, Zanxiang Nie, Shunyu Jin","doi":"10.1016/j.jmst.2024.11.030","DOIUrl":null,"url":null,"abstract":"Hydrogel electrolytes based on natural polymers have attracted increasing attention in zinc-ion batteries (ZIBs) powering wearable and implantable electronics, but designing natural polymer hydrogels with high ionic conductivity, excellent transference performance, and inhibited Zn dendrites is still challenging. Herein, two natural biocompatible polymers (sodium alginate (SA) and agarose (AG)) are used to prepare composite hydrogel electrolytes ensuring electrostatic interaction between –COO<sup>–</sup> groups in SA and Zn<sup>2+</sup> and coordination between C–O–C groups in AG and Zn<sup>2+</sup>. The as-obtained hydrogels exhibit an elevated ionic conductivity (25.05 mS cm<sup>−1</sup>) with a high transference number (0.75), useful for facilitated efficient Zn<sup>2+</sup> transport. The theoretical calculations combined with experimental results reveal C–O–C groups endowing the as-prepared hydrogels with improved desolvation kinetics and capture ability of Zn<sup>2+</sup> for achieving dendrite-free Zn deposition. In this way, the assembled Zn symmetric cell shows a long cycle life reaching 700 h at 0.2 mA cm<sup>−2</sup>. The exceptional biocompatibility of the hydrogels also results in cell viability assay with a survival rate above 93.5%. Overall, the proposed hydrogel electrolytes endow solid-state ZIBs with high discharge capacity, outstanding rate performance, long cycle life, good antifreeze capability, and impressive flexibility, useful features for future design and development of advanced ZIBs.","PeriodicalId":16154,"journal":{"name":"Journal of Materials Science & Technology","volume":"21 1","pages":""},"PeriodicalIF":11.2000,"publicationDate":"2024-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Science & Technology","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.jmst.2024.11.030","RegionNum":1,"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
Abstract
Hydrogel electrolytes based on natural polymers have attracted increasing attention in zinc-ion batteries (ZIBs) powering wearable and implantable electronics, but designing natural polymer hydrogels with high ionic conductivity, excellent transference performance, and inhibited Zn dendrites is still challenging. Herein, two natural biocompatible polymers (sodium alginate (SA) and agarose (AG)) are used to prepare composite hydrogel electrolytes ensuring electrostatic interaction between –COO– groups in SA and Zn2+ and coordination between C–O–C groups in AG and Zn2+. The as-obtained hydrogels exhibit an elevated ionic conductivity (25.05 mS cm−1) with a high transference number (0.75), useful for facilitated efficient Zn2+ transport. The theoretical calculations combined with experimental results reveal C–O–C groups endowing the as-prepared hydrogels with improved desolvation kinetics and capture ability of Zn2+ for achieving dendrite-free Zn deposition. In this way, the assembled Zn symmetric cell shows a long cycle life reaching 700 h at 0.2 mA cm−2. The exceptional biocompatibility of the hydrogels also results in cell viability assay with a survival rate above 93.5%. Overall, the proposed hydrogel electrolytes endow solid-state ZIBs with high discharge capacity, outstanding rate performance, long cycle life, good antifreeze capability, and impressive flexibility, useful features for future design and development of advanced ZIBs.
基于天然聚合物的水凝胶电解质在为可穿戴和植入式电子设备供电的锌离子电池(zbs)中引起了越来越多的关注,但设计具有高离子电导率、优异转移性能和抑制Zn枝晶的天然聚合物水凝胶仍然具有挑战性。本文采用海藻酸钠(SA)和琼脂糖(AG)两种天然生物相容性聚合物制备复合水凝胶电解质,保证了SA与Zn2+中- coo -基团之间的静电相互作用以及AG与Zn2+中C-O-C基团之间的配位。所得水凝胶具有较高的离子电导率(25.05 mS cm−1)和较高的转移数(0.75),有利于Zn2+的高效传输。理论计算与实验结果相结合表明,C-O-C基团使制备的水凝胶具有更好的脱溶动力学和Zn2+捕获能力,从而实现无枝晶Zn沉积。通过这种方法,组装的锌对称电池在0.2 mA cm−2下的循环寿命达到700小时。水凝胶优异的生物相容性也使其在细胞活力测定中具有93.5%以上的存活率。总体而言,所提出的水凝胶电解质赋予固态ZIBs高放电容量,出色的倍率性能,长循环寿命,良好的防冻能力和令人印象深刻的灵活性,为未来设计和开发先进的ZIBs提供了有用的特性。
期刊介绍:
Journal of Materials Science & Technology strives to promote global collaboration in the field of materials science and technology. It primarily publishes original research papers, invited review articles, letters, research notes, and summaries of scientific achievements. The journal covers a wide range of materials science and technology topics, including metallic materials, inorganic nonmetallic materials, and composite materials.