Hypothesis about electron quantum tunneling during sonochemical splitting of water molecule

Quantum tunneling in chemistry is often attributed to the processes at low or near room temperatures when the rate of thermal reactions becomes far less than the rate of quantum tunneling. However, in some rapid processes, quantum tunneling can be observed even at high temperatures. Herein, we report the experimental evidence for anomalous H/D kinetic isotope effect (KIE) during sonochemical dissociation of water molecule driven by 20 kHz power ultrasound measured in H₂O/D₂O mixtures saturated with Ar or Xe. Hydrogen released during ultrasonic treatment is enriched by light isotope. The observed H/D KIE (α = 2.15-1.50) is much larger than what is calculated assuming a classical KIE for T_g = 5000 K (α = 1.15) obtained from the sonoluminescence spectra in H₂O and D₂O. Furthermore, the α values sharply decrease with increasing of H₂O content in H₂O/D₂O mixtures reaching a steady-state value close to α = 1.50, which also cannot be explained by O-H/O-D zero-point energy difference. We suggest that these results can be understood in terms of quantum electron tunneling occurring in nonequilibrium picosecond plasma produced at the last stage of cavitation bubble collapse. Thermal homolytic splitting of water molecule is inhibited by extremely short lifetime of such plasma. On the contrary, immensely short traversal time for electron tunneling in water allows H₂O dissociation by quantum tunneling mechanism.