Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Phys Chem Lett ; 11(17): 7212-7217, 2020 Sep 03.
Artigo em Inglês | MEDLINE | ID: mdl-32787307

RESUMO

Photoluminescence upconversion in crystalline rubrene can proceed without an added sensitizer, but the mechanism for this process has not been well-understood. In particular, the species responsible for photon absorption has not been identified to date. To gain insight into the identity of the intermediate state, we measured the near-infrared (NIR) upconversion photoluminescence (UCPL) excitation spectrum of rubrene crystals and found three distinct spectral features. The UCPL yield has a quartic dependence on the laser intensity, implying a four-photon process. On the basis of electronic spectra of radical cations and anions of rubrene, we propose a mechanism in which photoexcited radical anions and cations undergo recombination, forming an excited neutral triplet while conserving spin. The triplets formed this way ultimately undergo triplet-triplet annihilation, resulting in the observed photoluminescence. This mechanism explains the origin of the NIR absorption as well as the four-photon nature of the UCPL process.

2.
J Phys Chem Lett ; 11(5): 1975-1980, 2020 Mar 05.
Artigo em Inglês | MEDLINE | ID: mdl-32066242

RESUMO

We report the size-dependent pressure response for CsPbBr3 perovskite nanocrystals in the size range 5.7-10.9 nm using photoluminescence spectroscopy in a diamond anvil cell. As the nanocrystal size decreases below ca. 7.5 nm, we observe a decrease in the transition pressure at which there is a change in the mode of deformation concomitant with an isostructural phase transition. We hypothesize that surface fluctuations regarding the tilt and distortion of surface PbBr6 octahedra facilitate the change in the mode of deformation and phase transition at lower pressures for smaller nanocrystals.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...