| Literature DB >> 26624490 |
Jun Pan1, Smritakshi P Sarmah1, Banavoth Murali1, Ibrahim Dursun1, Wei Peng1, Manas R Parida1, Jiakai Liu1, Lutfan Sinatra1, Noktan Alyami1, Chao Zhao2, Erkki Alarousu1, Tien Khee Ng3, Boon S Ooi3, Osman M Bakr1, Omar F Mohammed1.
Abstract
We demonstrate ultra-air- and photostable CsPbBr3 quantum dots (QDs) by using an inorganic-organic hybrid ion pair as the capping ligand. This passivation approach to perovskite QDs yields high photoluminescence quantum yield with unprecedented operational stability in ambient conditions (60 ± 5% lab humidity) and high pump fluences, thus overcoming one of the greatest challenges impeding the development of perovskite-based applications. Due to the robustness of passivated perovskite QDs, we were able to induce ultrastable amplified spontaneous emission (ASE) in solution processed QD films not only through one photon but also through two-photon absorption processes. The latter has not been observed before in the family of perovskite materials. More importantly, passivated perovskite QD films showed remarkable photostability under continuous pulsed laser excitation in ambient conditions for at least 34 h (corresponds to 1.2 × 10(8) laser shots), substantially exceeding the stability of other colloidal QD systems in which ASE has been observed.Entities:
Keywords: CsPbBr3; perovskite; photostability; quantum dots; surface passivation; two-photon absorption
Year: 2015 PMID: 26624490 DOI: 10.1021/acs.jpclett.5b02460
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475