4.6 Article

Vacuum ultraviolet photoabsorption spectroscopy of crystalline and amorphous benzene

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 19, Issue 40, Pages 27544-27555

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cp05319c

Keywords

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Funding

  1. Science and Technology Facilities Council

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We present the first high resolution vacuum ultraviolet photoabsorption study of amorphous benzene with com parisons to annealed crystalline benzene and the gas phase. Vapour deposited benzene layers w ere grow n at 25 K and annealed to 90 K under conditions pertinent to interstellaricy dust grains and icy planetary bodies in our solar system. Three single t-single t electronic transitions in solid benzene correspond to the B-1(2u), B-1(1u) and E-1(1u) states, redshifted by 0.05, 0.25 and 0.51 eV respectively with respect to the gas phase. The symmetry forbidden B-1(2u)<- (1)A(1g) and B-1(1u)<-(1)A(1g) transitions exhibit vibronic structure due to vibronic coupling and intensity borrowing from the allowed E-1(1u)<-(1)A(1g) transition. Additionally the B-1(2u)<- (1)A(1g) structure shows evidence of coupling between intramolecular vibrational and intermolecular lattice modes in crystalline benzene with Davydov crystal field splitting observed. The optically forbidden 0 - 0 electronic origin is clearly visible as a doublet at 4.69/4.70 eV in the crystalline solid and as a weak broadened feature at 4.67 eV in amorphous benzene. In the case of the Xu %g transition the forbidden 0 - 0 electronic origin is only observed in crystalline benzene as an exciton peak at 5.77 eV. Thicker amorphous benzene samples show diffuse bands around 4.3, 5.0 and 5.4 eV that we tentatively assign to spin forbidden single t-triplet B-3(2u)<- (1)A(1g), E-3(1u)<-(1)A(1g) and B-3(2u)<- (1)A(1g) transitions respectively, not previously reported in photoabsorption spectra of amorphous benzene. Further more, our results show clear evidence of non-wetting or 'islanding' of am orphous benzene, characterised by thickness-dependent Rayleigh scattering tails at wavelengths greater than 220 nm. These results have significant implications for our understanding of the physical and chemical properties and processes in astrochemical ices and highlight the importance of VUV spectroscopy.

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