All-inorganic CsPbBr3 perovskite quantum dots as a photoluminescent probe for ultrasensitive Cu2+ detection. Issue 17 (23rd April 2018)

• Record Type: Journal Article
• Authors: Liu, Yongfeng; Tang, Xiaosheng; Zhu, Tao; Deng, Ming; Ikechukwu, Iroegbu Paul; Huang, Wei; Yin, Guolu; Bai, Yongzhong; Qu, Dingrong; Huang, Xianbin; Qiu, Feng
• Is Part Of: Journal of materials chemistry. Volume 6:Issue 17(2018)
• Page Start: 4793
• Page End: 4799
• Publication Date: 2018-04-23
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Optical materials -- Research -- Periodicals; Electronics -- Materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8tc00249e
• Languages: English
• ISSNs: 2050-7526

Abstract

Abstract : Pollutions caused by heavy metals has become a wordwide concerned issue. Herein, CsPbBr3 perovskite quantum dots are used as fluorescent probe for selective detection of copper ions in organic phase with a limit of detection (LOD) down to 0.1 nM. Abstract : Pollution triggered by highly toxic heavy metal ions has become a worldwide issue of concern, and has aroused increasing research interest, but it is still a challenge to carry out its trace detection in the organic phase using inorganic fluorescent colloidal nanocrystals (NCs). Herein, we report fully inorganic CsPbBr3 perovskite quantum dots (PQDs), which were synthesized via a hot-injection method, as a fluorescent probe for the selective detection of copper ions in hexane. The photoluminescence (PL) intensity of CsPbBr3 PQDs is significantly quenched within several seconds after the addition of Cu 2+ due to effective electron transfer from the PQDs to the added Cu 2+, which is experimentally verified via analyzing absorption spectra and PL decay lifetime. The sensor, in turn-off mode, has a detection range from 0 to 100 nM with a limit of detection (LOD) as low as 0.1 nM, indicating great potential for practical applications. This study paves the way for PQD-based fluorescent probes for heavy metal detection in the organic phase.