Flexible molecular crystals for optoelectronic applications

材料科学 光电子学 纳米技术
作者
Chuanxin Wei,Liang Li,Yingying Zheng,Lizhi Wang,Jingyao Ma,Man Xu,Jinyi Lin,Linghai Xie,Pancě Naumov,Xue‐Hua Ding,Quanyou Feng,Wei Huang
出处
期刊:Chemical Society Reviews [Royal Society of Chemistry]
卷期号:53 (8): 3687-3713 被引量:92
标识
DOI:10.1039/d3cs00116d
摘要

The cornerstones of the advancement of flexible optoelectronics are the design, preparation, and utilization of novel materials with favorable mechanical and advanced optoelectronic properties. Molecular crystalline materials have emerged as a class of underexplored yet promising materials due to the reduced grain boundaries and defects anticipated to provide enhanced photoelectric characteristics. An inherent drawback that has precluded wider implementation of molecular crystals thus far, however, has been their brittleness, which renders them incapable of ensuring mechanical compliance required for even simple elastic or plastic deformation of the device. It is perplexing that despite a plethora of reports that have in the meantime become available underpinning the flexibility of molecular crystals, the "discovery" of elastically or plastically deformable crystals remains limited to cases of serendipitous and laborious trial-and-error approaches, a situation that calls for a systematic and thorough assessment of these properties and their correlation with the structure. This review provides a comprehensive and concise overview of the current understanding of the origins of crystal flexibility, the working mechanisms of deformations such as plastic and elastic bending behaviors, and insights into the examples of flexible molecular crystals, specifically concerning photoelectronic changes that occur in deformed crystals. We hope this summary will provide a reference for future experimental and computational efforts with flexible molecular crystals aimed towards improving their mechanical behavior and optoelectronic properties, ultimately intending to advance the flexible optoelectronic technology.
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
yu19完成签到,获得积分20
刚刚
星辰大海应助小羊采纳,获得10
刚刚
learning完成签到,获得积分10
刚刚
凯凯完成签到,获得积分10
1秒前
naya6600发布了新的文献求助10
2秒前
2秒前
bkagyin应助WQJ采纳,获得10
2秒前
背后妙旋发布了新的文献求助10
2秒前
juston应助精明的蜗牛采纳,获得10
3秒前
4秒前
SiO2完成签到 ,获得积分0
4秒前
小马甲应助yu19采纳,获得10
5秒前
6秒前
倒逆之蝶完成签到,获得积分10
7秒前
诚心绿兰完成签到,获得积分10
7秒前
英俊的铭应助月染孤云采纳,获得10
8秒前
乐乐应助七七采纳,获得10
10秒前
SciGPT应助皮卡皮卡采纳,获得10
10秒前
molihuakai应助yyydmhsj采纳,获得10
10秒前
Phiephie完成签到,获得积分10
11秒前
11秒前
脑洞疼应助Keats采纳,获得10
11秒前
12秒前
喜屿发布了新的文献求助10
12秒前
12秒前
13秒前
顾矜应助小小兵采纳,获得10
13秒前
13秒前
15秒前
15秒前
深情安青应助Huiming采纳,获得30
15秒前
vali完成签到,获得积分10
15秒前
ERTY完成签到,获得积分10
15秒前
CipherSage应助可达采纳,获得10
15秒前
Juvenilesy应助聪慧的过客采纳,获得10
16秒前
小南发布了新的文献求助10
17秒前
17秒前
瘦瘦的曼云完成签到,获得积分10
17秒前
18秒前
18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
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Navigating Normative Orders. Interdisciplinary Perspectives 800
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 700
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Organizational Behavior 510
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7743720
求助须知:如何正确求助?哪些是违规求助? 9291786
关于积分的说明 20209606
捐赠科研通 7322375
什么是DOI,文献DOI怎么找? 3307445
关于科研通互助平台的介绍 2459278
邀请新用户注册赠送积分活动 2318211