Single silica-coated Mn-doped CsPbCl3 perovskite quantum dots with enhanced stability and excellent optical properties

钙钛矿(结构) 量子点 材料科学 卤化物 兴奋剂 纳米颗粒 甲苯 配体(生物化学) 化学工程 分析化学(期刊) 纳米技术 化学 无机化学 结晶学 光电子学 有机化学 工程类 生物化学 受体
作者
Wenzhi Wang,Shuo Song,Jinkai Li,Bingqiang Cao,Zongming Liu
出处
期刊:Journal of Luminescence [Elsevier]
卷期号:252: 119361-119361 被引量:2
标识
DOI:10.1016/j.jlumin.2022.119361
摘要

Halide perovskite quantum dots (QDs) have been considered to be a potential emitting materials for illumination and display applications. Unfortunately, the toxicity and poor stability can greatly limit their practical application. Herein, the Mn2+-doped CsPbCl3 and SiO2-coated Cs(Pb,Mn)Cl3 perovskite QDs have been developed to solve the tricky problem without affecting their optical properties. Firstly, the mono-dispersed pure CsPbCl3 perovskite QDs with cubic morphologies are prepared by using a modified hot-injection method, as a control group. Next, the low-Pb content Cs(Pb,Mn)Cl3 perovskite QDs with distinctive dual emission peaks has been successfully obtained, including the CsPbCl3 host emission and the Mn2+ emission. Based on this, a new strategy for synthesizing single Cs(Pb,Mn)Cl3@SiO2 core-shell QDs with their initial cubic morphology and optical properties has been developed, which using the Cs(Pb,Mn)Cl3 nanoparticles as a precursor and choosing the APTES as the surface ligand. Photo-stability tests indicate that the Cs(Pb,Mn)Cl3 and Cs(Pb,Mn)Cl3@SiO2 perovskite QDs are markedly more stable than the pure CsPbCl3 QDs, indicating that the crystal engineering and host packaging are all effective way to improve the stability. Meanwhile, the PL intensity of Cs(Pb,Mn)Cl3@SiO2 dispersed in a mixed solution of toluene and water can retained 63% of the initial value even after 14 h, which are much higher than Cs(Pb,Mn)Cl3 (31%). Therefore, the Cs(Pb,Mn)Cl3 after SiO2 coating is the more effective way to improve stability than that of the Mn2+ doping. This work not only provides a simple and reliable synthesis way to synthesize the single core-shell particles, which can be suitable for other perovskite systems, but also compares the two methods of the crystal engineering and the host packaging to improve the stability of perovskite QDs for practical application.
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
kaifeiQi完成签到,获得积分10
刚刚
猴子魏应助酷酷若风采纳,获得50
1秒前
Liam发布了新的文献求助10
1秒前
paper完成签到,获得积分10
4秒前
华仔应助科研通管家采纳,获得10
5秒前
李健应助科研通管家采纳,获得10
5秒前
一一应助科研通管家采纳,获得20
5秒前
Owen应助科研通管家采纳,获得10
5秒前
cyrong应助科研通管家采纳,获得10
5秒前
科研通AI2S应助科研通管家采纳,获得10
5秒前
完美世界应助科研通管家采纳,获得10
5秒前
Orange应助科研通管家采纳,获得10
5秒前
852应助SHL采纳,获得10
6秒前
穆紫应助陈陈陈采纳,获得10
6秒前
99giddens发布了新的文献求助50
8秒前
guoer完成签到,获得积分10
9秒前
慕青应助聪明的绝悟采纳,获得10
10秒前
祯果粒完成签到,获得积分10
11秒前
REN应助新雨采纳,获得20
11秒前
11秒前
12秒前
和谐雁荷完成签到 ,获得积分10
12秒前
英俊的铭应助rfr采纳,获得10
14秒前
15秒前
研友_VZG7GZ应助回眸是明眸采纳,获得10
15秒前
aizaixiyuanqian完成签到,获得积分20
16秒前
现代书雪发布了新的文献求助10
17秒前
18秒前
Jasper应助Crazyalien采纳,获得10
18秒前
乐乐应助wxx采纳,获得10
20秒前
20秒前
SHL完成签到,获得积分10
21秒前
科研張应助tt采纳,获得20
21秒前
23秒前
大红红蝴蝶公主完成签到,获得积分10
23秒前
23秒前
24秒前
24秒前
新斯的明的明完成签到 ,获得积分10
24秒前
瘦瘦的易槐完成签到,获得积分20
24秒前
高分求助中
Sustainability in Tides Chemistry 2000
Bayesian Models of Cognition:Reverse Engineering the Mind 800
Essentials of thematic analysis 700
A Dissection Guide & Atlas to the Rabbit 600
Very-high-order BVD Schemes Using β-variable THINC Method 568
Внешняя политика КНР: о сущности внешнеполитического курса современного китайского руководства 500
Revolution und Konterrevolution in China [by A. Losowsky] 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 3124525
求助须知:如何正确求助?哪些是违规求助? 2774840
关于积分的说明 7724243
捐赠科研通 2430307
什么是DOI,文献DOI怎么找? 1291019
科研通“疑难数据库(出版商)”最低求助积分说明 622052
版权声明 600297