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Universal dynamical onset in water at distinct material interfaces.

Lirong ZhengZhuo LiuQiang ZhangSong LiJuan HuangLei ZhangBing ZanMadhusudan TyagiHe ChengTaisen ZuoVictoria García SakaiTakeshi YamadaChenxing YangPan TanFan JiangHao ChenWei ZhuangLiang Hong
Published in: Chemical science (2022)
Interfacial water remains liquid and mobile much below 0 °C, imparting flexibility to the encapsulated materials to ensure their diverse functions at subzero temperatures. However, a united picture that can describe the dynamical differences of interfacial water on different materials and its role in imparting system-specific flexibility to distinct materials is lacking. By combining neutron spectroscopy and isotope labeling, we explored the dynamics of water and the underlying substrates independently below 0 °C across a broad range of materials. Surprisingly, while the function-related anharmonic dynamical onset in the materials exhibits diverse activation temperatures, the surface water presents a universal onset at a common temperature. Further analysis of the neutron experiment and simulation results revealed that the universal onset of water results from an intrinsic surface-independent relaxation: switching of hydrogen bonds between neighboring water molecules with a common energy barrier of ∼35 kJ mol -1 .
Keyphrases
  • ionic liquid
  • molecular dynamics simulations
  • mass spectrometry
  • molecular dynamics
  • electron transfer