Xinyu Wang , Yiran Ying , Yuanbiao Gong , Shengmei Chen , Shuyun Wang , Weijia Wang , Juan Antonio Zapien , Longtao Ma , Min Zhu
{"title":"环境适应稳定锌电池的压电梯度电解质","authors":"Xinyu Wang , Yiran Ying , Yuanbiao Gong , Shengmei Chen , Shuyun Wang , Weijia Wang , Juan Antonio Zapien , Longtao Ma , Min Zhu","doi":"10.1016/j.ensm.2025.104586","DOIUrl":null,"url":null,"abstract":"<div><div>Solid polymer electrolyte-based zinc batteries are promising candidates for next-generation electrochemical energy storage due to their cost-effectiveness, enhanced safety and high theoretical energy density. However, their practical deployment is severely hindered by sluggish Zn<sup>2+</sup> ion mobility, poor interfacial compatibility and uneven electric field distribution. To address the persistent challenges, this work presents a novel asymmetric piezoelectric electrolyte, engineered by the strategic vertical distribution of piezoelectric barium titanate (BTO) nanofillers within a polyvinylidene fluoride (PVDF)-based polymer matrix. This design introduces a built-in gradient electric field across the electrolyte thickness, leveraging the electromechanical properties of BTO to regulate ion transport and interfacial dynamics. On the Zn anode-facing side, the BTO-rich region with a high dielectric constant and enhanced local polarization, promotes zinc salt dissociation and generates a directional electric field that promotes uniform Zn<sup>2+</sup> flux. This configuration effectively suppresses dendrite formation and mitigates localized charge accumulation. Conversely, the MnO<sub>2</sub> cathode-facing side comprises a softer, polymer-rich phase with lower BTO content, ensuring better interfacial compliance and reduced contact resistance, which is crucial for facilitating efficient ion transport without inducing excessive polarization. As a result, the asymmetric architecture achieves an impressive ionic conductivity of 1.39 mS·cm<sup>-1</sup> and a high Zn<sup>2+</sup> transference number of 0.69 at room temperature, outperforming conventional SPEs. ZnǀǀZn symmetric cells exhibit outstanding cycle stability, sustaining operation for over 1500 h, while Zn||MnO<sub>2</sub> full batteries demonstrate stable cycling over 1200 cycles. Notably, the battery performs reliably across a wide temperature range from -30 °C to 60 °C, demonstrating strong adaptability to harsh environments. This work provides a scalable and effective strategy for overcoming key limitations in Zn-based batteries by introducing a functionally asymmetric, piezoelectric electrolyte structure. This advancement paves the way for the development of safe, durable, and high-efficiency zinc-ion batteries.</div></div>","PeriodicalId":306,"journal":{"name":"Energy Storage Materials","volume":"82 ","pages":"Article 104586"},"PeriodicalIF":20.2000,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Piezoelectric gradient electrolytes for environmentally adaptive and stable zinc batteries\",\"authors\":\"Xinyu Wang , Yiran Ying , Yuanbiao Gong , Shengmei Chen , Shuyun Wang , Weijia Wang , Juan Antonio Zapien , Longtao Ma , Min Zhu\",\"doi\":\"10.1016/j.ensm.2025.104586\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Solid polymer electrolyte-based zinc batteries are promising candidates for next-generation electrochemical energy storage due to their cost-effectiveness, enhanced safety and high theoretical energy density. However, their practical deployment is severely hindered by sluggish Zn<sup>2+</sup> ion mobility, poor interfacial compatibility and uneven electric field distribution. To address the persistent challenges, this work presents a novel asymmetric piezoelectric electrolyte, engineered by the strategic vertical distribution of piezoelectric barium titanate (BTO) nanofillers within a polyvinylidene fluoride (PVDF)-based polymer matrix. This design introduces a built-in gradient electric field across the electrolyte thickness, leveraging the electromechanical properties of BTO to regulate ion transport and interfacial dynamics. On the Zn anode-facing side, the BTO-rich region with a high dielectric constant and enhanced local polarization, promotes zinc salt dissociation and generates a directional electric field that promotes uniform Zn<sup>2+</sup> flux. This configuration effectively suppresses dendrite formation and mitigates localized charge accumulation. Conversely, the MnO<sub>2</sub> cathode-facing side comprises a softer, polymer-rich phase with lower BTO content, ensuring better interfacial compliance and reduced contact resistance, which is crucial for facilitating efficient ion transport without inducing excessive polarization. As a result, the asymmetric architecture achieves an impressive ionic conductivity of 1.39 mS·cm<sup>-1</sup> and a high Zn<sup>2+</sup> transference number of 0.69 at room temperature, outperforming conventional SPEs. ZnǀǀZn symmetric cells exhibit outstanding cycle stability, sustaining operation for over 1500 h, while Zn||MnO<sub>2</sub> full batteries demonstrate stable cycling over 1200 cycles. Notably, the battery performs reliably across a wide temperature range from -30 °C to 60 °C, demonstrating strong adaptability to harsh environments. This work provides a scalable and effective strategy for overcoming key limitations in Zn-based batteries by introducing a functionally asymmetric, piezoelectric electrolyte structure. This advancement paves the way for the development of safe, durable, and high-efficiency zinc-ion batteries.</div></div>\",\"PeriodicalId\":306,\"journal\":{\"name\":\"Energy Storage Materials\",\"volume\":\"82 \",\"pages\":\"Article 104586\"},\"PeriodicalIF\":20.2000,\"publicationDate\":\"2025-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy Storage Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2405829725005847\",\"RegionNum\":1,\"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":"Energy Storage Materials","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2405829725005847","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Piezoelectric gradient electrolytes for environmentally adaptive and stable zinc batteries
Solid polymer electrolyte-based zinc batteries are promising candidates for next-generation electrochemical energy storage due to their cost-effectiveness, enhanced safety and high theoretical energy density. However, their practical deployment is severely hindered by sluggish Zn2+ ion mobility, poor interfacial compatibility and uneven electric field distribution. To address the persistent challenges, this work presents a novel asymmetric piezoelectric electrolyte, engineered by the strategic vertical distribution of piezoelectric barium titanate (BTO) nanofillers within a polyvinylidene fluoride (PVDF)-based polymer matrix. This design introduces a built-in gradient electric field across the electrolyte thickness, leveraging the electromechanical properties of BTO to regulate ion transport and interfacial dynamics. On the Zn anode-facing side, the BTO-rich region with a high dielectric constant and enhanced local polarization, promotes zinc salt dissociation and generates a directional electric field that promotes uniform Zn2+ flux. This configuration effectively suppresses dendrite formation and mitigates localized charge accumulation. Conversely, the MnO2 cathode-facing side comprises a softer, polymer-rich phase with lower BTO content, ensuring better interfacial compliance and reduced contact resistance, which is crucial for facilitating efficient ion transport without inducing excessive polarization. As a result, the asymmetric architecture achieves an impressive ionic conductivity of 1.39 mS·cm-1 and a high Zn2+ transference number of 0.69 at room temperature, outperforming conventional SPEs. ZnǀǀZn symmetric cells exhibit outstanding cycle stability, sustaining operation for over 1500 h, while Zn||MnO2 full batteries demonstrate stable cycling over 1200 cycles. Notably, the battery performs reliably across a wide temperature range from -30 °C to 60 °C, demonstrating strong adaptability to harsh environments. This work provides a scalable and effective strategy for overcoming key limitations in Zn-based batteries by introducing a functionally asymmetric, piezoelectric electrolyte structure. This advancement paves the way for the development of safe, durable, and high-efficiency zinc-ion batteries.
期刊介绍:
Energy Storage Materials is a global interdisciplinary journal dedicated to sharing scientific and technological advancements in materials and devices for advanced energy storage and related energy conversion, such as in metal-O2 batteries. The journal features comprehensive research articles, including full papers and short communications, as well as authoritative feature articles and reviews by leading experts in the field.
Energy Storage Materials covers a wide range of topics, including the synthesis, fabrication, structure, properties, performance, and technological applications of energy storage materials. Additionally, the journal explores strategies, policies, and developments in the field of energy storage materials and devices for sustainable energy.
Published papers are selected based on their scientific and technological significance, their ability to provide valuable new knowledge, and their relevance to the international research community.