We report the reversible
photochemical transformation of sulfur–hydrogen
mixture to (H2S)2H2, which occurs
through an expanded state of photoactive a-S phase
of sulfur at 4 GPa. Upon further compression, the photoproduct (H2S)2H2 undergoes a phase transition at
17 GPa, and 40 GPa. The pressure-induced Raman changes indicate that
the phase transition from phase I to II at 17 GPa is associated with
the proton-ordering process in (H2S)2H2, evident by the profound splitting of S–H and H–H
vibrational modes, whereas the transition at 40 GPa is accompanied
by the disappearance of all the S–H stretching and bending
modes and partial dissociation to sulfur. With increase in pressure,
the molar volume of (H2S)2H2 is substantially
larger than that of S + H2 mixtures, suggesting the significance
of photochemical effect in order to drive the reaction from S + H2 to (H2S)2H2. In addition,
we have also provided the thermal- and pressure-induced effect in
the mixtures using confocal Raman spectroscopy. From our results,
it is clear that the effect of pressure and photochemistry can be
coupled to drive the reaction at room temperature and lower pressure,
rather than having to drive the reaction thermally or mechanically,
underscoring the significance of the photochemical effect in understanding
the path-dependent transformations of sulfur and sulfur-containing
materials.