Kinetics of electron–hole pair trapping via photoionization of biphenyl occluded in aluminium-rich ZSM-5 zeolites. Effects of extra-framework cations

文献信息

发布日期 2004-05-10
DOI 10.1039/B401816H
影响因子 3.676
作者

Isabelle Gener, Alain Moissette, Claude Brémard


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摘要

The effects of the extraframework cations M+ = Li+, Na+, K+, Rb+, Cs+ of aluminium rich M6.6ZSM-5 zeolites on the long-lived photoproducts of occluded biphenyl (BP) have been investigated by conventional diffuse reflectance UV-visible (DRUVv) absorption and continuous wave electron paramagnetic resonance (CW-EPR). Many DRUVv and EPR spectra were recorded over two days after the UV laser photoionization (248 nm, 15 s, 30 mW cm−2) of dehydrated M6.6(AlO2)6.6(SiO2)89.4 samples loaded with 1 BP per unit cell. The application of EPR measurements provided evidence of durable BP˙+-electron moiety through well resolved seven line signal (BP˙+) superimposed on a broad overlapping feature (trapped electron). The EPR spectra recorded during the development of the irradiated samples at room temperature indicated the BP˙+ disappearance and the persistence of broad signal. These persistent structureless signals were assigned to very long-lived electron–hole pairs. The application of the SIMPLISMA approach to DRUVv data sets recorded after the photolysis resolved two pure absorption spectra assigned to BP˙+ and electron–hole pairs (420–500 nm) for all the irradiated samples. All the decays of corresponding concentrations were found to fit accurately a model of first order dispersed heterogeneous kinetics. The BP˙+ disappearance rate constants were found to increase with larger alkali metal cations (Li+ ∼ Na+ < K+ ∼ Rb+ ≪ Cs+) and correlated to the electron-donating ability of the framework. The electron abstraction by BP˙+ did not induce direct charge recombination but generated persistent electron–hole pair over at most 1 h (Li+) and at least 1 min (Cs+). The electron–hole pair recombination went to completion over more than two days (M = Li+) and less than 1 h (M = K+). The recombination rate was found to be in relation with the electron donor properties of framework but probably involved other parameters.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
自引率: 10.3%
年发文量: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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