Synergistic Alignment of Low Aspect‐Ratio π‐Conjugated Molecules Enables Exceptional UV–vis–NIR Polarization Detection

共轭体系 极化(电化学) 分子 材料科学 纵横比(航空) 光电子学 纳米技术 光学 化学 物理 聚合物 有机化学 复合材料 物理化学
作者
Yingying Xue,Qiong Zuo,Qi Zhu,Yukun Li,Zilin Deng,Zibang Zhang,Zhiyuan Yang,Cheng Wang,Rui Zhang,Xianjie Liu,Jingang Zhong,Wenkai Zhong,Lei Ying,Wanzhu Cai
出处
期刊:Laser & Photonics Reviews [Wiley]
卷期号:20 (1) 被引量:1
标识
DOI:10.1002/lpor.202500938
摘要

Abstract Polarization detection enhances signal contrast and is widely utilized in diverse advanced applications. An ongoing challenge is the development of high‐performance polarization‐sensitive photodetectors based on optically anisotropic organic semiconductors, particularly in the near‐infrared (NIR) region. While uniaxially aligned π‐conjugated polymers with high aspect ratios exhibit strong linear dichroism and have shown promise, their limited NIR performance and heavy reliance on polymer material now represent critical limitations. Here, a breakthrough is reported in achieving giant linear dichroism and exceptional polarization detection with low aspect‐ratios (AR) non‐fullerene small‐molecule (NFSM) acceptors, extending polarization sensitivity from the UV–vis to the NIR range. An impressive dichroic ratio of 27.1 at 605 nm and 12.0 at 780 nm is demonstrated. The maximum polarization photocurrent ratio is 11.2 at 780 nm under parallel versus perpendicular polarized light. This unprecedented performance originates from synergistic molecular alignment, wherein NFSMs significantly enhance the uniaxial orientation of both the polymer matrix and the NFSMs themselves during self‐assembly and thermal annealing. Besides, such a linear‐polarization‐sensitive photodetectors (LPS‐PDs) are showcased in generating degree‐of‐linear‐polarization imaging. The work establishes NFSMs as a viable material system for next‐generation of organic LPS‐PDs and provides fundamental insights into structural origins of polarization sensitivity in low AR organic semiconductors.
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
philios发布了新的文献求助10
刚刚
赘婿应助小海螺采纳,获得10
1秒前
1秒前
4秒前
7秒前
甜蜜一兰发布了新的文献求助10
8秒前
8秒前
Rain完成签到,获得积分10
8秒前
666发布了新的文献求助10
10秒前
10秒前
11秒前
自由归尘发布了新的文献求助10
11秒前
科研通AI6.4应助小样采纳,获得10
12秒前
研友_司空笑柳完成签到,获得积分20
12秒前
JamesPei应助科研通管家采纳,获得10
13秒前
13秒前
JamesPei应助科研通管家采纳,获得10
13秒前
小蘑菇应助科研通管家采纳,获得10
13秒前
Lucas应助科研通管家采纳,获得10
13秒前
13秒前
研友_VZG7GZ应助科研通管家采纳,获得10
13秒前
13秒前
13秒前
所所应助科研通管家采纳,获得10
13秒前
13秒前
今后应助科研通管家采纳,获得10
13秒前
lsx完成签到,获得积分10
14秒前
斯文败类应助科研通管家采纳,获得10
14秒前
溯尘星落应助科研通管家采纳,获得20
14秒前
14秒前
NexusExplorer应助科研通管家采纳,获得10
14秒前
柠栀应助科研通管家采纳,获得10
14秒前
大模型应助科研通管家采纳,获得10
14秒前
14秒前
14秒前
小星星发布了新的文献求助30
14秒前
鹿笙完成签到,获得积分10
15秒前
philios完成签到,获得积分20
16秒前
16秒前
科研通AI6.3应助sx12138采纳,获得10
18秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
Molecular Mechanisms of Photosynthesis, 4th Edition 1000
Organic Reactions, Volume 116 1000
Matrix Methods in Data Mining and Pattern Recognition 510
Reading and Understanding Health Research 500
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 7252054
求助须知:如何正确求助?哪些是违规求助? 8874443
关于积分的说明 18732196
捐赠科研通 6931990
什么是DOI,文献DOI怎么找? 3199585
关于科研通互助平台的介绍 2374362
邀请新用户注册赠送积分活动 2174177