• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

具有网络异质纳米结构电极的生物相容对称钠离子微电池,实现了用于植入式生物电子学的高可靠性和高能量密度。

Biocompatible Symmetric Na-Ion Microbatteries with Sphere-in-Network Heteronanomat Electrodes Realizing High Reliability and High Energy Density for Implantable Bioelectronics.

机构信息

Key Laboratory for Photonic and Electronic Bandgap Materials, Ministry of Education, College of Chemistry and Chemical Engineering , Harbin Normal University , Harbin 150025 , Heilongjiang , China.

College of Material Science and Chemical Engineering , Harbin Engineering University , Harbin 150001 , Heilongjiang , China.

出版信息

ACS Appl Mater Interfaces. 2018 Dec 12;10(49):42268-42278. doi: 10.1021/acsami.8b14918. Epub 2018 Nov 29.

DOI:10.1021/acsami.8b14918
PMID:30457330
Abstract

The prolonged life expectancy accelerates the development of implantable bioelectronic devices. However, conventional batteries with limited lifetime, rigid architecture, and inferior energy density greatly restrict their applications in patient's body. Herein, a novel flexible symmetric Na-ion microbattery based on the heteronanomat electrode and the biocompatible electrolyte has been developed. The film electrodes with sphere-in-network architecture are synthesized by simultaneously electrospinning and electrospraying followed by carbonization. The combined technologies allow a uniform incorporation of active materials/C spheres into the carbon nanofiber matrix, which results in the heteronanomat electrodes with robust structure, fast electron/ion transport, and compact mass loading. The flexible microbatteries are fabricated based on the interdigitated microelectrodes and the biocompatible electrolytes, which provides a new implantable power source for bioelectronics. As a proof-of-concept study, the symmetric sodium-ion microbatteries are constructed from the heteronanomat bifunctional electrodes (based on NaVTi(PO)) and the biocompatible electrolyte. The high reversibility, fast kinetics, and high energy density of the symmetric system in the biocompatible electrolytes reveal their superior performance in bioenvironments. Moreover, the high capacity retention (over 98%) and the high stability of microbattery implanted in a living SD rat for a month further demonstrate its high reliability for long-term in vivo diagnosis. Therefore, this work not only presents a new sphere-in-net heteronanomat structure for fabricating high-performance electrode but also gives significant contributions to develop high-energy-density and high safety biocompatible power sources of implantable bioelectronics.

摘要

预期寿命的延长加速了可植入生物电子设备的发展。然而,传统电池的寿命有限、结构僵硬、能量密度低,极大地限制了它们在患者体内的应用。在此,开发了一种基于杂纳米结构电极和生物相容性电解质的新型柔性对称钠离子微型电池。通过同时静电纺丝和静电喷雾以及碳化合成具有球网结构的薄膜电极。组合技术允许将活性材料/C 球均匀地掺入到碳纳米纤维基质中,从而得到具有坚固结构、快速电子/离子传输和紧凑质量负载的杂纳米结构电极。基于叉指微电极和生物相容性电解质制造了柔性微电池,为生物电子学提供了新的可植入电源。作为概念验证研究,使用杂纳米结构双功能电极(基于 NaVTi(PO)) 和生物相容性电解质构建了对称钠离子微型电池。在生物相容性电解质中,对称系统具有高可逆性、快速动力学和高能量密度,这表明它们在生物环境中的性能优越。此外,在活 SD 大鼠体内植入一个月后,微型电池的高容量保持率(超过 98%)和高稳定性进一步证明了其在长期体内诊断中的高可靠性。因此,这项工作不仅提出了一种用于制造高性能电极的新型球网杂纳米结构,而且为开发可植入生物电子学的高能量密度和高安全性生物相容性电源做出了重要贡献。

相似文献

1
Biocompatible Symmetric Na-Ion Microbatteries with Sphere-in-Network Heteronanomat Electrodes Realizing High Reliability and High Energy Density for Implantable Bioelectronics.具有网络异质纳米结构电极的生物相容对称钠离子微电池,实现了用于植入式生物电子学的高可靠性和高能量密度。
ACS Appl Mater Interfaces. 2018 Dec 12;10(49):42268-42278. doi: 10.1021/acsami.8b14918. Epub 2018 Nov 29.
2
Flexible/Rechargeable Zn-Air Batteries Based on Multifunctional Heteronanomat Architecture.基于多功能杂化纳米结构的柔性/可充电锌空气电池。
ACS Appl Mater Interfaces. 2018 Jul 5;10(26):22210-22217. doi: 10.1021/acsami.8b05215. Epub 2018 Jun 21.
3
Recent Advances of Energy Solutions for Implantable Bioelectronics.可植入生物电子学的能源解决方案的最新进展。
Adv Healthc Mater. 2021 Sep;10(17):e2100199. doi: 10.1002/adhm.202100199. Epub 2021 Apr 30.
4
Exploring role of microbatteries in enhancing sustainability and functionality of implantable biosensors and bioelectronics.探索微电池在提高植入式生物传感器和生物电子学的可持续性和功能性方面的作用。
Biosens Bioelectron. 2024 Sep 15;260:116419. doi: 10.1016/j.bios.2024.116419. Epub 2024 May 22.
5
Stress-Actuated Spiral Microelectrode for High-Performance Lithium-Ion Microbatteries.用于高性能锂离子微型电池的应力驱动螺旋微电极。
Small. 2020 Sep;16(35):e2002410. doi: 10.1002/smll.202002410. Epub 2020 Jul 23.
6
High-Performance Packaged 3D Lithium-Ion Microbatteries Fabricated Using Imprint Lithography.采用压印光刻技术制造的高性能封装3D锂离子微电池。
Adv Mater. 2021 Jan;33(1):e2006229. doi: 10.1002/adma.202006229. Epub 2020 Nov 26.
7
Materials Strategies and Device Architectures of Emerging Power Supply Devices for Implantable Bioelectronics.新兴植入式生物电子学供电设备的材料策略和器件架构。
Small. 2020 Apr;16(15):e1902827. doi: 10.1002/smll.201902827. Epub 2019 Sep 12.
8
Wearable Textile-Based Co-Zn Alkaline Microbattery with High Energy Density and Excellent Reliability.具有高能量密度和卓越可靠性的可穿戴织物基钴锌碱性微型电池
Small. 2020 Apr;16(16):e2000293. doi: 10.1002/smll.202000293. Epub 2020 Mar 20.
9
Stamped microbattery electrodes based on self-assembled M13 viruses.基于自组装M13病毒的冲压微电池电极。
Proc Natl Acad Sci U S A. 2008 Nov 11;105(45):17227-31. doi: 10.1073/pnas.0711620105. Epub 2008 Aug 27.
10
High rate and stable symmetric potassium ion batteries fabricated with flexible electrodes and solid-state electrolytes.采用柔性电极和固态电解质制备高倍率和稳定的对称钾离子电池。
Nanoscale. 2018 Nov 15;10(44):20754-20760. doi: 10.1039/c8nr07268j.

引用本文的文献

1
Photolithographic Microfabrication of Microbatteries for On-Chip Energy Storage.用于片上能量存储的微型电池的光刻微制造
Nanomicro Lett. 2025 Jan 8;17(1):105. doi: 10.1007/s40820-024-01625-9.
2
Pharmacokinetics of Eight Flavonoids in Rats Assayed by UPLC-MS/MS after Oral Administration of Extract.超高效液相色谱-串联质谱法测定大鼠口服提取物后八种黄酮类化合物的药代动力学
J Anal Methods Chem. 2018 Dec 18;2018:4789196. doi: 10.1155/2018/4789196. eCollection 2018.