期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 140, 期 1, 页码 406-412出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b11003
关键词
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资金
- Ministry of Science and Technology of China [2016YFE0129600]
- National Natural Science Foundation of China [21401135, 21673150]
- 111 Project
- SWC for Synchrotron Radiation Research
- Collaborative Innovation Center of Suzhou Nano Science and Technology (NANO-CIC)
- Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
- American Chemical Society Petroleum Research Fund [55904-ND10]
The poor stability of CsPbX3 (X = Cl, Br, I) nanocrystals (NCs) has severely impeded their practical applications. Although there are some successful examples on encapsulating multiple CsPbX3 NCs into an oxide or polymer matrix, it has remained a serious challenge for the surface modification/encapsulation using oxides or polymers at a single particle level. In this work, monodisperse CsPbX3/SiO2 and CsPbBr3/Ta2O5 Janus nanoparticles were successfully prepared by combining a water-triggered transformation process and a sol-gel method. The CsPbBr3/SiO2 NCs exhibited a photoluminescence quantum yield of 80% and a lifetime of 19.8 ns. The product showed dramatically improved stability against destruction by air, water, and light irradiation. Upon continuous irradiation by intense UV light for 10 h, a film of the CsPbBr3/SiO2 Janus NCs showed only a slight drop (2%) in the PL intensity, while a control sample of unmodified CsPbBr3 NCs displayed a 35% drop. We further highlighted the advantageous features of the CsPbBr3/SiO2 NCs in practical applications by using them as the green light source for the fabrication of a prototype white light emitting diode, and demonstrated a wide color gamut covering up to 138% of the National Television System Committee standard. This work not only provides a novel approach for the surface modification of individual CsPbX3 NCs but also helps to address the challenging stability issue; therefore, it has an important implication toward their practical applications.
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