Photoionization of methylphenothiazine in palladium ion-exchanged SAPO-5 and SAPO-11 silicoaluminophosphate microporous materials

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Palladium ion-exchanged SAPO-5 and SAPO-11 silicoaluminophosphate microporous materials were examined for the photoionization of N-methylphenothiazine (PC1) with 320 nm irradiation at room temperature. Photoionization of Pd-containing SAPO-5 and SAPO-11 materials results in the formation of N-methylphenothiazine radical cations (PC1+). The radicals were identified by electron spin resonance (ESR). The PC1+ yield was found to increase with increasing Pd content suggesting that the Pd ion serves as the electron acceptor site. The photoefficiency depends on the nature of the Pd species, the Pd content, and the channel size of the SAPO material. It is noteworthy that the photoyield of methylphenothiazine cation radical is higher in solid-state ion-exchanged Pd-SAPO materials compared to other hosts including alpha-ZrP, NiVPI-5, M-ETS-10, Ti-MCM-41, VAPO-5, CrH-SAPO-8, Cu-X and CuH-UHM-3.
Publisher
AMER CHEMICAL SOC
Issue Date
2002-01
Language
English
Article Type
Article
Keywords

ELECTRON-SPIN-RESONANCE; DIFFERENT PORE SIZES; PHOTOCATALYTIC REDUCTION; PHOTOELECTRON TRANSFER; CHARGE SEPARATION; TRANSITION-METAL; SILICA-GELS; ZEOLITE; ASSEMBLIES; WATER

Citation

JOURNAL OF PHYSICAL CHEMISTRY B, v.106, no.3, pp.583 - 588

ISSN
1520-6106
DOI
10.1021/jp0113883
URI
http://hdl.handle.net/10203/79721
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