posted on 2017-04-18, 00:00authored byMelissa
L. Liriano, Chiara Gattinoni, Emily A. Lewis, Colin J. Murphy, E. Charles H. Sykes, Angelos Michaelides
Water has an incredible ability to
form a rich variety of structures,
with 16 bulk ice phases identified, for example, as well as numerous
distinct structures for water at interfaces or under confinement.
Many of these structures are built from hexagonal motifs of water
molecules, and indeed, for water on metal surfaces, individual hexamers
of just six water molecules have been observed. Here, we report the
results of low-temperature scanning tunneling microscopy experiments
and density functional theory calculations which reveal a host of
new structures for water–ice nanoclusters when adsorbed on
an atomically flat Cu surface. The H-bonding networks within the nanoclusters
resemble the resonance structures of polycyclic aromatic hydrocarbons,
and water–ice analogues of inene, naphthalene, phenalene, anthracene,
phenanthrene, and triphenylene have been observed. The specific structures
identified and the H-bonding patterns within them reveal new insight
about water on metals that allows us to refine the so-called “2D
ice rules”, which have so far proved useful in understanding
water–ice structures at solid surfaces.