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J Kerry Thomas

Publications and source records attributed to J Kerry Thomas.

2 recordsLinked to original sources

Effect of SiO2 and zeolite surfaces on the excited triplet state of benzophenone, BT; a spectroscopic and kinetic study.

Laser flash photolysis has been used to study the triplet excited state of benzophenone B(T), on various surfaces, SiO(2), zeolites NaY, KY, NaX and KX, and in rigid media at room temperature, polyethylene and polymethylmethacrylate. The studies point to similarities of the spectroscopy and kinetics of B(T) in fluid solution, in a solid matrix (polymers) and on a SiO(2) surface. However, stark differences are observed for B(T) in zeolites where the absorption spectrum mimics that of the protonated ketone, and the reactivities of B(T) with C(6)H(12) and CH(3)OH are an order of magnitude smaller than those in liquid C(6)H(12) and CH(3)OH. Inclusion of ammonia, which blocks acidic sites in the zeolite, produces a triplet spectrum which is similar to that in polar solution. The reactivity of the triplet with ammonia in a zeolite is also comparable to that observed for this reaction in polar solution. These data are discussed in terms of the interaction of benzophenone with acidic sites in the zeolites, and to restrictions placed on the reactants in the zeolite cages. The blocking of the zeolite acidic sites by ammonia produces spectral and kinetic data (reactivity with NH(3)) of the triplet that are comparable to those observed in solution. This is one of the few cases where zeolites inhibit rather than promote reactions of a solute adsorbed in them.

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Photoinduced electron transfer at solid surfaces: the TiO2-SiO2 system.

Small particles of TiO2 have been synthesized on porous silica. XRD and spectral measurements place the sizes of the particles at about 50 A. With these small particles the band gap of the semiconductor material is markedly blue shifted with respect to bulk TiO2. This enables the direct excitation of co-adsorbed arenes on the TiO2-SiO2 material. Direct excitation of TiO2 leads to Ti3+, by photoinduced extraction from the SiO2. Direct excitation of pyrene on the material leads to a shortened fluorescence lifetime and lower quantum yield. Meanwhile, the yield of pyrene cation radical increases compared to that on pure SiO2. The production of Ti3+ on the pyrene samples, by direct excitation of the TiO2, leads to a shortened pyrene fluorescence lifetime and decreased quantum yield, the quantum yield decreasing to zero at high enough Ti3+. Removal of Ti3+ by O2 causes the original properties of the pyrene fluorescence to return.

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