Nuclear Quantum Effects in Hydrophobic Nanoconfinement
Author(s) -
Buddha Ratna Shrestha,
Sreekiran Pillai,
Adriano Santana,
Stephen H. Donaldson,
Tod A. Pascal,
Himanshu Mishra
Publication year - 2019
Publication title -
the journal of physical chemistry letters
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.9b01835
Subject(s) - delocalized electron , quantum tunnelling , chemical physics , quantum , molecular dynamics , chemistry , kinetic isotope effect , proton , zero point energy , hydrophobic effect , nanotechnology , materials science , physics , condensed matter physics , atomic physics , computational chemistry , quantum mechanics , deuterium , organic chemistry
Nuclear quantum effects (NQEs) in water arise due to delocalization, zero-point energy (ZPE), and quantum tunneling of protons. Whereas quantum tunneling is significant only at low temperatures, proton delocalization and ZPE influence the properties of water at normal temperature and pressure (NTP), giving rise to isotope effects. However, the consequences of NQEs for interfaces of water with hydrophobic media, such as perfluorocarbons, have remained largely unexplored. Here, we reveal the existence and signature of NQEs modulating hydrophobic surface forces at NTP. Our experiments demonstrate that the attractive hydrophobic forces between molecularly smooth and rigid perfluorinated surfaces in nanoconfinement are ≈10% higher in H 2 O than in D 2 O, even though the contact angles of H 2 O and D 2 O on these surfaces are indistinguishable. Our molecular dynamics simulations show that the underlying cause of the difference includes the destabilizing effect of ZPE on the librational motions of interfacial H 2 O, which experiences larger quantum effects than D 2 O.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom