学术文献库

Signatures of solvated excess protons in infrared difference absorption spectra, such as the continuum band between the water bend and stretch bands, have been experimentally known for a long time, but the theoretical basis for linking spectral signatures with the microscopic proton-transfer mechanism so far relied on normal-mode analysis. We analyze the excess-proton dynamics in ab initio molecular-dynamics simulations of aqueous hydrochloric acid solutions by trajectory-decomposition techniques. The continuum band in the 2000 - 3000 cm$^{-1 }$ range is shown to be due to normal-mode oscillations of temporary H$_3$O$^+$ complexes. An additional prominent peak at 400 cm$^{-1}$ reports on the coupling of excess-proton motion to the relative vibrations of the two flanking water molecules. The actual proton transfer between two water molecules, which for large water separations involves crossing of a barrier and thus is not a normal mode, is characterized by two characteristic time scales: Firstly, the waiting time for transfer to occur in the range of 200 - 300 fs, which leads to a broad weak shoulder around ~100 cm$^{-1}$, consistent with our experimental THz spectra. Secondly, the mean duration of a transfer event of about 14 fs, which produces a rather well-defined spectral contribution around 1200 cm$^{-1}$ and agrees in location and width with previous experimental mid-infrared spectra.