Photoluminescence Spectroscopy of Silica-Based Mesoporous Materials
Author(s) -
Yuri D. Glinka,
ShengHsien Lin,
LianPin Hwang,
YitTsong Chen
Publication year - 2000
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/jp0009599
Subject(s) - photoluminescence , materials science , spectroscopy , mesoporous silica , exciton , excitation , yttrium , photoluminescence excitation , mesoporous material , analytical chemistry (journal) , molecular physics , optoelectronics , oxide , chemistry , condensed matter physics , physics , biochemistry , chromatography , quantum mechanics , metallurgy , catalysis
The photoluminescence (PL) at 300 and 90 K from the mesoporous silicas (MSs) [ordered (MCM-41) and disordered (DMSs)] of variously sized pores induced either by ArF laser light (λexc = 193 nm) or by Nd:YAG (yttrium−aluminum−garnet) laser light (λexc = 266 nm) was studied. The spectra were measured in both conventional and time-resolved detection modes. It has been shown that PL induced by 266-nm light results from a direct one-photon excitation of hydrogen-related species (the green band) situated on the internal pore surfaces and nonbridging oxygen hole centers (NBOHCs, the red bands) located both on the surface and inside ∼1-nm sized bulk fragments (pore walls). Alternatively, an indirect excitation of the light emitters due to the energy transfer through two-photon-produced free excitons (FEs) is responsible for PL in the case of 193-nm excitation. In addition, the self-trapping of FEs followed by radiative relaxation results in the blue band, which can only be induced by 193-nm light. The PL propertie...
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