TY - JOUR
T1 - Experimental Evidence of Long-Lived Electric Fields of Ionic Liquid Bilayers
AU - Belotti, Mattia
AU - Lyu, Xin
AU - Xu, Longkun
AU - Halat, Peter
AU - Darwish, Nadim
AU - Silvester, Debbie S.
AU - Goh, Ching
AU - Izgorodina, Ekaterina I.
AU - Coote, Michelle L.
AU - Ciampi, Simone
PY - 2021/10/27
Y1 - 2021/10/27
N2 - Herein we demonstrate that ionic liquids can form long-lived double layers, generating electric fields detectable by straightforward open circuit potential (OCP) measurements. In imidazolium-based ionic liquids an external negative voltage pulse leads to an exceedingly stable near-surface dipolar layer, whose field manifests as long-lived (∼1-100 h) discrete plateaus in OCP versus time traces. These plateaus occur within an ionic liquid-specific and sharp potential window, defining a simple experimental method to probe the onset of interfacial ordering phenomena, such as overscreening and crowding. Molecular dynamics modeling reveals that the OCP arises from the alignment of the individual ion dipoles to the external electric field pulse, with the magnitude of the resulting OCP correlating with the product of the projected dipole moment of the cation and the ratio between the cation diffusion coefficient and its volume. Our findings also reveal that a stable overscreened structure is more likely to form if the interface is first forced through crowding, possibly accounting for the scattered literature data on relaxation kinetics of near-surface structures in ionic liquids.
AB - Herein we demonstrate that ionic liquids can form long-lived double layers, generating electric fields detectable by straightforward open circuit potential (OCP) measurements. In imidazolium-based ionic liquids an external negative voltage pulse leads to an exceedingly stable near-surface dipolar layer, whose field manifests as long-lived (∼1-100 h) discrete plateaus in OCP versus time traces. These plateaus occur within an ionic liquid-specific and sharp potential window, defining a simple experimental method to probe the onset of interfacial ordering phenomena, such as overscreening and crowding. Molecular dynamics modeling reveals that the OCP arises from the alignment of the individual ion dipoles to the external electric field pulse, with the magnitude of the resulting OCP correlating with the product of the projected dipole moment of the cation and the ratio between the cation diffusion coefficient and its volume. Our findings also reveal that a stable overscreened structure is more likely to form if the interface is first forced through crowding, possibly accounting for the scattered literature data on relaxation kinetics of near-surface structures in ionic liquids.
KW - Ionic Liquid Bilayers
KW - electric fields
KW - open circuit potential
KW - OCP
UR - http://www.scopus.com/inward/record.url?scp=85118247920&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/ARC/DP190100735
UR - http://purl.org/au-research/grants/ARC/FT190100148
UR - http://purl.org/au-research/grants/ARC/FL170100041
U2 - 10.1021/jacs.1c06385
DO - 10.1021/jacs.1c06385
M3 - Article
C2 - 34657417
AN - SCOPUS:85118247920
VL - 143
SP - 17431
EP - 17440
JO - Journal of The American Chemical Society
JF - Journal of The American Chemical Society
SN - 0002-7863
IS - 42
ER -