Heating-free synthesis of red emissive carbon dots through separated processes of polymerization and carbonization

碳化 聚合 化学工程 聚合物 材料科学 硫酸 高分子化学 化学 有机化学 工程类 吸附
作者
Hongcan Sun,Pengfei Xia,Haibao Shao,Rong Zhang,Changgui Lü,Shuhong Xu,Chunlei Wang
出处
期刊:Journal of Colloid and Interface Science [Elsevier]
卷期号:646: 932-939 被引量:21
标识
DOI:10.1016/j.jcis.2023.05.120
摘要

Polymerization and carbonization are believed as two basic processes for the bottom-up synthesis of carbon dots (CDs). Since these two processes usually occur simultaneously due to the high reaction temperature and fast reaction rate, it is still a challenge to separate and control these two processes. In the present work, we reported a new room temperature method, which achieved the separated and controlled polymerization and carbonization processes. The polymerization process is realized by dissolving o-phenylenediamine (OPD) in ethanol at room temperature, and finally obtained polymer dots (PDs) without any lattice with a sphere size of 29.6 nm. The carbonization process begins in a manual way by adding concentrated sulfuric acid. After carbonization, CDs (noted as CPDs in this work) with a size of 3.6 nm and a clear lattice can be obtained. Importantly, the separated polymerization and carbonization make us possible to adjust the composition or interactions of intermediate products during the synthesis process. As a prototype, we added acetic acid (AA) additives into OPD precursors during the polymerization stage. Due to the crosslink enhanced emission (CEE) effect via hydrogen bonds which are produced by the amide groups from AA reaction products with H in the –NH3+ or aromatic ring, the resulted CPDs show improved PLQY from an initial 6.87% (without AA) to 16.47%. The current work realized the separated and controllable polymerization and carbonization processes, opening up the door for tuning the composition and interactions of intermediate products before carbonization.
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
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
XC发布了新的文献求助10
刚刚
慕青应助坚强的皮皮虾采纳,获得10
刚刚
1秒前
我打完成签到,获得积分10
3秒前
3秒前
山见山完成签到 ,获得积分10
3秒前
认真写论文的小梁完成签到,获得积分10
3秒前
大鸡炖蘑菇完成签到,获得积分10
3秒前
彳亍1117应助婉儿采纳,获得10
4秒前
许容发布了新的文献求助10
5秒前
5秒前
5秒前
5秒前
5秒前
祝顺遂完成签到 ,获得积分10
5秒前
6秒前
星辰大海应助GG采纳,获得10
6秒前
超chao完成签到,获得积分10
7秒前
英俊皮卡丘完成签到,获得积分10
7秒前
7秒前
7秒前
7秒前
我打发布了新的文献求助30
8秒前
8秒前
QL发布了新的文献求助10
8秒前
vickyyao发布了新的文献求助10
10秒前
10秒前
10秒前
追寻皮卡丘完成签到,获得积分10
11秒前
六个核桃发布了新的文献求助10
11秒前
小马甲应助meimhuang采纳,获得10
11秒前
乖拉发布了新的文献求助10
12秒前
wanci应助现实的访云采纳,获得10
12秒前
小于发布了新的文献求助10
12秒前
JoJo发布了新的文献求助10
12秒前
彳亍发布了新的文献求助10
12秒前
12秒前
13秒前
14秒前
jianjiao发布了新的文献求助10
14秒前
高分求助中
Evolution 10000
ISSN 2159-8274 EISSN 2159-8290 1000
Becoming: An Introduction to Jung's Concept of Individuation 600
Ore genesis in the Zambian Copperbelt with particular reference to the northern sector of the Chambishi basin 500
A new species of Coccus (Homoptera: Coccoidea) from Malawi 500
A new species of Velataspis (Hemiptera Coccoidea Diaspididae) from tea in Assam 500
PraxisRatgeber: Mantiden: Faszinierende Lauerjäger 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3160487
求助须知:如何正确求助?哪些是违规求助? 2811659
关于积分的说明 7892950
捐赠科研通 2470589
什么是DOI,文献DOI怎么找? 1315639
科研通“疑难数据库(出版商)”最低求助积分说明 630910
版权声明 602042