Optically healable supramolecular polymers

超分子聚合物 超分子化学 聚合物 材料科学 高分子科学 化学 分子 复合材料 有机化学
作者
Mark Burnworth,Li‐Ming Tang,Justin R. Kumpfer,Andrew J. Duncan,Frederick L. Beyer,Gina L. Fiore,Stuart J. Rowan,Christoph Weder
出处
期刊:Nature [Springer Nature]
卷期号:472 (7343): 334-337 被引量:1686
标识
DOI:10.1038/nature09963
摘要

Smart materials with an in-built ability to repair damage caused by normal wear and tear could prove useful in a wide range of applications. Most healable polymer-based materials so far developed require heating of the damaged area. But Burnworth et al. have now produced materials — in the form of polymer strands linked through metal complexes — that can be mended through exposure to light. The metal complexes in these materials can absorb ultraviolet light that is then converted into heat, which temporarily unlinks the polymer strands for quick and efficient defect healing. In principle, healing can take place in situ and while under load. Polymers with the ability to repair themselves after sustaining damage could extend the lifetimes of materials used in many applications1. Most approaches to healable materials require heating the damaged area2,3,4. Here we present metallosupramolecular polymers that can be mended through exposure to light. They consist of telechelic, rubbery, low-molecular-mass polymers with ligand end groups that are non-covalently linked through metal-ion binding. On exposure to ultraviolet light, the metal–ligand motifs are electronically excited and the absorbed energy is converted into heat. This causes temporary disengagement of the metal–ligand motifs and a concomitant reversible decrease in the polymers’ molecular mass and viscosity5, thereby allowing quick and efficient defect healing. Light can be applied locally to a damage site, so objects can in principle be healed under load. We anticipate that this approach to healable materials, based on supramolecular polymers and a light–heat conversion step, can be applied to a wide range of supramolecular materials that use different chemistries.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
传奇3应助hero3采纳,获得10
1秒前
小梨子发布了新的文献求助10
1秒前
zhouti497541171完成签到,获得积分10
2秒前
刘若鑫发布了新的文献求助10
2秒前
2秒前
2秒前
2秒前
学术小垃圾完成签到,获得积分10
3秒前
小马甲应助AAAAA采纳,获得10
3秒前
情怀应助根号3采纳,获得10
3秒前
3秒前
耶耶小豆包完成签到 ,获得积分10
3秒前
4秒前
哇_你梦里啊完成签到 ,获得积分10
4秒前
4秒前
踏雾发布了新的文献求助10
4秒前
4秒前
墨白白完成签到,获得积分10
4秒前
呆萌问丝发布了新的文献求助10
4秒前
徐小徐发布了新的文献求助10
5秒前
5秒前
36456657应助高小明采纳,获得10
5秒前
6秒前
汤传麒完成签到,获得积分10
6秒前
林二发布了新的文献求助10
6秒前
7秒前
FashionBoy应助wj采纳,获得10
7秒前
lhy完成签到,获得积分10
7秒前
游云发布了新的文献求助30
8秒前
帅气冰蝶完成签到,获得积分10
8秒前
大漠孤烟望完成签到,获得积分10
8秒前
sci大户发布了新的文献求助10
8秒前
酷波er应助吞吞采纳,获得30
8秒前
f123456789发布了新的文献求助10
9秒前
9秒前
10秒前
10秒前
斯文败类应助徐小徐采纳,获得10
10秒前
酷炫语琴完成签到,获得积分10
10秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The Cambridge History of China: Volume 4, Sui and T'ang China, 589–906 AD, Part Two 1000
The Composition and Relative Chronology of Dynasties 16 and 17 in Egypt 1000
Russian Foreign Policy: Change and Continuity 800
Real World Research, 5th Edition 800
Qualitative Data Analysis with NVivo By Jenine Beekhuyzen, Pat Bazeley · 2024 800
Superabsorbent Polymers 700
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5710379
求助须知:如何正确求助?哪些是违规求助? 5199013
关于积分的说明 15260454
捐赠科研通 4863009
什么是DOI,文献DOI怎么找? 2610375
邀请新用户注册赠送积分活动 1560754
关于科研通互助平台的介绍 1518381