TY - JOUR
T1 - A robust molecular probe for Ångstrom-scale analytics in liquids
AU - Nirmalraj, Peter
AU - Thompson, Damien
AU - Dimitrakopoulos, Christos
AU - Gotsmann, Bernd
AU - Dumcenco, Dumitru
AU - Kis, Andras
AU - Riel, Heike
N1 - Publisher Copyright:
© 2016 The Author(s).
PY - 2016/8/12
Y1 - 2016/8/12
N2 - Traditionally, nanomaterial profiling using a single-molecule-terminated scanning probe is performed at the vacuum-solid interface often at a few Kelvin, but is not a notion immediately associated with liquid-solid interface at room temperature. Here, using a scanning tunnelling probe functionalized with a single C60 molecule stabilized in a high-density liquid, we resolve low-dimensional surface defects, atomic interfaces and capture Ångstrom-level bond-length variations in single-layer graphene and MoS2. Atom-by-atom controllable imaging contrast is demonstrated at room temperature and the electronic structure of the C60-metal probe complex within the encompassing liquid molecules is clarified using density functional theory. Our findings demonstrates that operating a robust single-molecular probe is not restricted to ultra-high vacuum and cryogenic settings. Hence the scope of high-precision analytics can be extended towards resolving sub-molecular features of organic elements and gauging ambient compatibility of emerging layered materials with atomic-scale sensitivity under experimentally less stringent conditions.
AB - Traditionally, nanomaterial profiling using a single-molecule-terminated scanning probe is performed at the vacuum-solid interface often at a few Kelvin, but is not a notion immediately associated with liquid-solid interface at room temperature. Here, using a scanning tunnelling probe functionalized with a single C60 molecule stabilized in a high-density liquid, we resolve low-dimensional surface defects, atomic interfaces and capture Ångstrom-level bond-length variations in single-layer graphene and MoS2. Atom-by-atom controllable imaging contrast is demonstrated at room temperature and the electronic structure of the C60-metal probe complex within the encompassing liquid molecules is clarified using density functional theory. Our findings demonstrates that operating a robust single-molecular probe is not restricted to ultra-high vacuum and cryogenic settings. Hence the scope of high-precision analytics can be extended towards resolving sub-molecular features of organic elements and gauging ambient compatibility of emerging layered materials with atomic-scale sensitivity under experimentally less stringent conditions.
UR - http://www.scopus.com/inward/record.url?scp=84982273795&partnerID=8YFLogxK
U2 - 10.1038/ncomms12403
DO - 10.1038/ncomms12403
M3 - Article
AN - SCOPUS:84982273795
SN - 2041-1723
VL - 7
JO - Nature Communications
JF - Nature Communications
M1 - 12403
ER -