Toward Covalent Organic Framework Metastructures

聚合物 纳米尺度 纳米技术 纳米孔 化学 共价键 单体 纳米颗粒 光子学 纳米结构 化学工程 光电子学 材料科学 有机化学 工程类
作者
Song Wang,Yuhao Yang,Haoran Zhang,Ziyang Zhang,Chi Zhang,Xiaodong Huang,Daichi Kozawa,Pingwei Liu,Bo‐Geng Li,Wenjun Wang
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:143 (13): 5003-5010 被引量:67
标识
DOI:10.1021/jacs.0c13090
摘要

The bottom-up assembly of periodically ordered structures provides a scalable way for producing metastructured materials with exotic optical and mechanical properties. However, direct self-assembly of small molecules into such metastructures beyond the nanoscale remains an unresolved issue. Here we demonstrate that metastructured assemblies of two-dimensional (2D) polymers, specifically 2D covalent organic frameworks (COFs), can be directly synthesized in solution. We applied 2D COF monomer polycondensation to prepare flower-shaped particles consisting of highly crystalline "petals" with sizes larger than 20 μm. The petal comprises periodically arranged COF nanoflake units with tunable lengths of 490-850 nm, thicknesses about 20 nm, interflake spacing around 14 nm, and Hermans orientation factors up to 0.998. Such a metastructure is mechanically robust and remains almost intact even after full pyrolysis at 900 °C. It also demonstrates unique birefringence and polarization-dependent resonances under visible-near-infrared light not observed in its constituents, 2D COF polycrystals, and with well-defined nanopores of 1.8 nm and the high surface area of 1576 m2/g. Such metastructured particles with nanopores are well-suited as novel particulate optical devices for collecting and storing information about their surroundings that can be easily read out by polarization imaging with high sensitivity, as demonstrated by their explosive detection and anticounterfeiting applications. Self-assembly of 2D polymers into metastructures may become an important method for developing functional materials with unprecedented properties and extensive applications.
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
1秒前
李爱国应助蜗牛小霸王采纳,获得10
1秒前
领导范儿应助zxx采纳,获得10
2秒前
Prejudice3完成签到,获得积分10
2秒前
斯文败类应助壮观手套采纳,获得10
2秒前
清新的灵寒完成签到,获得积分10
2秒前
三金完成签到,获得积分10
3秒前
Tonsil01完成签到,获得积分10
3秒前
5秒前
方俊驰完成签到,获得积分10
5秒前
汉堡包应助科研通管家采纳,获得10
5秒前
5秒前
慕青应助科研通管家采纳,获得10
6秒前
香蕉觅云应助科研通管家采纳,获得10
6秒前
爆米花应助科研通管家采纳,获得10
6秒前
6秒前
6秒前
6秒前
CipherSage应助科研通管家采纳,获得10
6秒前
6秒前
小蘑菇应助科研通管家采纳,获得10
6秒前
英姑应助科研通管家采纳,获得10
6秒前
6秒前
FashionBoy应助科研通管家采纳,获得10
6秒前
科目三应助科研通管家采纳,获得10
6秒前
6秒前
Tonsil01发布了新的文献求助10
7秒前
7秒前
duila给duila的求助进行了留言
8秒前
科研通AI6.1应助wln采纳,获得10
8秒前
上官若男应助Jack采纳,获得10
8秒前
王彦林应助英勇语山采纳,获得10
8秒前
gyh应助wahaha采纳,获得20
9秒前
隐形曼青应助壮观手套采纳,获得10
9秒前
大力的灵雁应助chenxilulu采纳,获得10
10秒前
英俊的铭应助bxdrl采纳,获得10
11秒前
啵啵小甜狗完成签到,获得积分10
12秒前
HYD发布了新的文献求助10
12秒前
qys关闭了qys文献求助
12秒前
九三完成签到 ,获得积分10
12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
Aerospace Standards Index - 2026 ASIN2026 3000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Research Methods for Business: A Skill Building Approach, 9th Edition 500
Social Work and Social Welfare: An Invitation(7th Edition) 410
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6047886
求助须知:如何正确求助?哪些是违规求助? 7828614
关于积分的说明 16257915
捐赠科研通 5193301
什么是DOI,文献DOI怎么找? 2778847
邀请新用户注册赠送积分活动 1762077
关于科研通互助平台的介绍 1644438