554 research outputs found
Local probing of ionic diffusion by electrochemical strain microscopy: spatial resolution and signal formation mechanisms
Electrochemical insertion-deintercalation reactions are typically associated
with significant change of molar volume of the host compound. This strong
coupling between ionic currents and strains underpins image formation
mechanisms in electrochemical strain microscopy (ESM), and allows exploring the
tip-induced electrochemical processes locally. Here we analyze the signal
formation mechanism in ESM, and develop the analytical description of operation
in frequency and time domains. The ESM spectroscopic modes are compared to
classical electrochemical methods including potentiostatic and galvanostatic
intermittent titration (PITT and GITT), and electrochemical impedance
spectroscopy (EIS). This analysis illustrates the feasibility of spatially
resolved studies of Li-ion dynamics on the sub-10 nanometer level using
electromechanical detection.Comment: 49 pages, 17 figures, 4 tables, 3 appendices, to be submitted to J.
Appl. Phys
Recommended from our members
In situ tracking of the nanoscale expansion of porous carbon electrodes
Electrochemical double layer capacitors (EDLC) are rapidly emerging as a promising energy storage technology offering extremely large power densities. Despite significant experimental progress, nanoscale operation mechanisms of the EDLCs remain poorly understood and it is difficult to separate processes at multiple time and length scales involved in operation including that of double layer charging and ionic mass transport. Here we explore the functionality of EDLC microporous carbon electrodes using a combination of classical electrochemical measurements and scanning probe microscopy based dilatometry, thus separating individual stages in charge/discharge processes based on strain generation. These methods allowed us to observe two distinct modes of EDLC charging, one fast charging of the double layer unassociated with strain, and another much slower mass transport related charging exhibiting significant sample volume changes. These studies open the pathway for the exploration of electrochemical systems with multiple processes involved in the charge and discharge, and investigation of the kinetics of those processes
Giant thermally-enhanced electrostriction and polar surface phase in La2Mo2O9 oxygen ion conductors
Ferroelectrics possess spontaneous electric polarization at macroscopic scales which nonetheless imposes strict limitations on the material classes. Recent discoveries of untraditional symmetry-breaking phenomena in reduced material dimensions have indicated feasibilities to extend polar properties to broader types of materials, potentially opening up the freedom for designing materials with hybrid functionalities. Here, we report the unusual electromechanical properties of La2Mo2O9 (LAMOX) oxygen ion conductors, systematically investigated at both bulk and surface length levels. We first observed giant electrostriction effects in La2Mo2O9 bulk ceramics that are thermally enhanced in concert with their low-energy oxygen-vacancy hopping dynamics. Moreover, while no clear bulk polarization was detected, the surface phases of LAMOX were found to be manifestly polar, likely originating from the coupling between the intrinsic structural flexibilities with strain gradients (i.e., flexoelectricity) and/or chemical heterogeneities present in the materials. These findings identify La2Mo2O9 as a promising electromechanical material system and suggest that the flexible structural and chemical configurations in ionically active materials could enable fundamentally different venues to accommodate electric polarization.Q.L. and H.W. were supported by the US Department of Energy, Office of Science, Materials Science and Engineering Division. T.L. and Y.L. acknowledge the support of the Australian Research Council (ARC) in the form of Discovery Projects (DP160104780). N.L. was supported by the Eugene P. Wigner Fellowship program at ORNL (No. DE-AC05-00OR22725). The PFM experiments were performed at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility at Oak Ridge National Laboratory (ORNL). The use of Advanced Photon Source was supported by the US DOE, Basic Energy Science under Contract No. DE-AC02-06CH11357
Parameters of the Magnetic Flux inside Coronal Holes
Parameters of magnetic flux distribution inside low-latitude coronal holes
(CHs) were analyzed. A statistical study of 44 CHs based on Solar and
Heliospheric Observatory (SOHO)/MDI full disk magnetograms and SOHO/EIT 284\AA
images showed that the density of the net magnetic flux, , does
not correlate with the associated solar wind speeds, . Both the area and
net flux of CHs correlate with the solar wind speed and the corresponding
spatial Pearson correlation coefficients are 0.75 and 0.71, respectively. A
possible explanation for the low correlation between and
is proposed. The observed non-correlation might be rooted in the structural
complexity of the magnetic field. As a measure of complexity of the magnetic
field, the filling factor, , was calculated as a function of spatial
scales. In CHs, was found to be nearly constant at scales above 2 Mm,
which indicates a monofractal structural organization and smooth temporal
evolution. The magnitude of the filling factor is 0.04 from the Hinode SOT/SP
data and 0.07 from the MDI/HR data. The Hinode data show that at scales smaller
than 2 Mm, the filling factor decreases rapidly, which means a mutlifractal
structure and highly intermittent, burst-like energy release regime. The
absence of necessary complexity in CH magnetic fields at scales above 2 Mm
seems to be the most plausible reason why the net magnetic flux density does
not seem to be related to the solar wind speed: the energy release dynamics,
needed for solar wind acceleration, appears to occur at small scales below 1
Mm.Comment: 6 figures, approximately 23 pages. Accepted in Solar Physic
- …