通过二维MXene驱动的电子积聚和LiNbO₃辅助的电荷转移提高可拉伸纳米发电机的三电性能

IF 12.7 1区 材料科学 Q1 ENGINEERING, MULTIDISCIPLINARY
Biswajit Mahanty , Sujoy Kumar Ghosh , Dong-Weon Lee
{"title":"通过二维MXene驱动的电子积聚和LiNbO₃辅助的电荷转移提高可拉伸纳米发电机的三电性能","authors":"Biswajit Mahanty ,&nbsp;Sujoy Kumar Ghosh ,&nbsp;Dong-Weon Lee","doi":"10.1016/j.compositesb.2024.111995","DOIUrl":null,"url":null,"abstract":"<div><div>The development of piezoelectrically enhanced triboelectric hybrid nanogenerators (PET-HNGs) has garnered considerable attention for their potential in energy harvesting. However, their performance in stretchable applications across diverse environments, such as air and water, remains limited due to the lack of high-performance, stretchable material compositions and a comprehensive understanding of the charge transfer mechanism involved. To address these challenges, we have designed a high-performance, stretchable nano-/micro-composite film by embedding 2D MXene nanosheets and piezoelectric LiNbO<sub>3</sub> microparticles into an Ecoflex polymer matrix. Quantum mechanical calculations revealed that MXene nanosheets significantly increase electron density near the Fermi level, while LiNbO<sub>3</sub> microparticles enhance electron transfer during contact electrification with polydimethylsiloxane (PDMS). This synergistic effect resulted in a substantial enhancement of the triboelectric energy harvesting performance, with the composite film exhibiting a 355 % increase in voltage, a 324 % increase in current, and a 100 % boost in power output density compared to systems using pure Ecoflex based TENGs. The fabricated PET-HNG demonstrated remarkable output metrics, including a voltage of 455 V, current of 140 μA, power output density of 15.6 W m<sup>−2</sup>, and an energy conversion efficiency of 78.5 %, all while maintaining exceptional performance stability even under mechanical stretching.</div><div>This stretchable nanogenerator shows great potential as a self-powered wearable sensor for real-time biomechanical monitoring in various environments, including air and underwater. This innovation paves the way for the development of next-generation wearable electronics and energy harvesting devices.</div></div>","PeriodicalId":10660,"journal":{"name":"Composites Part B: Engineering","volume":"291 ","pages":"Article 111995"},"PeriodicalIF":12.7000,"publicationDate":"2024-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Boosted triboelectric performance in stretchable nanogenerators via 2D MXene-Driven electron accumulation and LiNbO₃-assisted charge transfer\",\"authors\":\"Biswajit Mahanty ,&nbsp;Sujoy Kumar Ghosh ,&nbsp;Dong-Weon Lee\",\"doi\":\"10.1016/j.compositesb.2024.111995\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The development of piezoelectrically enhanced triboelectric hybrid nanogenerators (PET-HNGs) has garnered considerable attention for their potential in energy harvesting. However, their performance in stretchable applications across diverse environments, such as air and water, remains limited due to the lack of high-performance, stretchable material compositions and a comprehensive understanding of the charge transfer mechanism involved. To address these challenges, we have designed a high-performance, stretchable nano-/micro-composite film by embedding 2D MXene nanosheets and piezoelectric LiNbO<sub>3</sub> microparticles into an Ecoflex polymer matrix. Quantum mechanical calculations revealed that MXene nanosheets significantly increase electron density near the Fermi level, while LiNbO<sub>3</sub> microparticles enhance electron transfer during contact electrification with polydimethylsiloxane (PDMS). This synergistic effect resulted in a substantial enhancement of the triboelectric energy harvesting performance, with the composite film exhibiting a 355 % increase in voltage, a 324 % increase in current, and a 100 % boost in power output density compared to systems using pure Ecoflex based TENGs. The fabricated PET-HNG demonstrated remarkable output metrics, including a voltage of 455 V, current of 140 μA, power output density of 15.6 W m<sup>−2</sup>, and an energy conversion efficiency of 78.5 %, all while maintaining exceptional performance stability even under mechanical stretching.</div><div>This stretchable nanogenerator shows great potential as a self-powered wearable sensor for real-time biomechanical monitoring in various environments, including air and underwater. This innovation paves the way for the development of next-generation wearable electronics and energy harvesting devices.</div></div>\",\"PeriodicalId\":10660,\"journal\":{\"name\":\"Composites Part B: Engineering\",\"volume\":\"291 \",\"pages\":\"Article 111995\"},\"PeriodicalIF\":12.7000,\"publicationDate\":\"2024-11-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Composites Part B: Engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1359836824008084\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Composites Part B: Engineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1359836824008084","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

压电增强三电混合纳米发电机(PET-HNGs)在能量收集方面的发展潜力引起了广泛关注。然而,由于缺乏高性能、可拉伸的材料成分以及对相关电荷转移机制的全面了解,它们在空气和水等不同环境中的可拉伸应用性能仍然有限。为了应对这些挑战,我们将二维 MXene 纳米片和压电 LiNbO3 微颗粒嵌入 Ecoflex 聚合物基质中,设计出了一种高性能、可拉伸的纳米/微复合薄膜。量子力学计算显示,MXene 纳米片显著提高了费米级附近的电子密度,而 LiNbO3 微颗粒则增强了与聚二甲基硅氧烷(PDMS)接触电化过程中的电子转移。这种协同效应大大提高了三电能收集性能,与使用纯 Ecoflex TENG 的系统相比,复合薄膜的电压提高了 355%,电流提高了 324%,功率输出密度提高了 100%。制造出的 PET-HNG 显示出卓越的输出指标,包括 455 V 的电压、140 μA 的电流、15.6 W m-2 的功率输出密度和 78.5 % 的能量转换效率,同时即使在机械拉伸的情况下也能保持卓越的性能稳定性。这项创新为开发下一代可穿戴电子设备和能量收集装置铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Boosted triboelectric performance in stretchable nanogenerators via 2D MXene-Driven electron accumulation and LiNbO₃-assisted charge transfer
The development of piezoelectrically enhanced triboelectric hybrid nanogenerators (PET-HNGs) has garnered considerable attention for their potential in energy harvesting. However, their performance in stretchable applications across diverse environments, such as air and water, remains limited due to the lack of high-performance, stretchable material compositions and a comprehensive understanding of the charge transfer mechanism involved. To address these challenges, we have designed a high-performance, stretchable nano-/micro-composite film by embedding 2D MXene nanosheets and piezoelectric LiNbO3 microparticles into an Ecoflex polymer matrix. Quantum mechanical calculations revealed that MXene nanosheets significantly increase electron density near the Fermi level, while LiNbO3 microparticles enhance electron transfer during contact electrification with polydimethylsiloxane (PDMS). This synergistic effect resulted in a substantial enhancement of the triboelectric energy harvesting performance, with the composite film exhibiting a 355 % increase in voltage, a 324 % increase in current, and a 100 % boost in power output density compared to systems using pure Ecoflex based TENGs. The fabricated PET-HNG demonstrated remarkable output metrics, including a voltage of 455 V, current of 140 μA, power output density of 15.6 W m−2, and an energy conversion efficiency of 78.5 %, all while maintaining exceptional performance stability even under mechanical stretching.
This stretchable nanogenerator shows great potential as a self-powered wearable sensor for real-time biomechanical monitoring in various environments, including air and underwater. This innovation paves the way for the development of next-generation wearable electronics and energy harvesting devices.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Composites Part B: Engineering
Composites Part B: Engineering 工程技术-材料科学:复合
CiteScore
24.40
自引率
11.50%
发文量
784
审稿时长
21 days
期刊介绍: Composites Part B: Engineering is a journal that publishes impactful research of high quality on composite materials. This research is supported by fundamental mechanics and materials science and engineering approaches. The targeted research can cover a wide range of length scales, ranging from nano to micro and meso, and even to the full product and structure level. The journal specifically focuses on engineering applications that involve high performance composites. These applications can range from low volume and high cost to high volume and low cost composite development. The main goal of the journal is to provide a platform for the prompt publication of original and high quality research. The emphasis is on design, development, modeling, validation, and manufacturing of engineering details and concepts. The journal welcomes both basic research papers and proposals for review articles. Authors are encouraged to address challenges across various application areas. These areas include, but are not limited to, aerospace, automotive, and other surface transportation. The journal also covers energy-related applications, with a focus on renewable energy. Other application areas include infrastructure, off-shore and maritime projects, health care technology, and recreational products.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信