daohang fenxiangbox searchbox qikanlogonew daohangnew searchboxnew navrightzone footerzone paper

Surface Dynamics of Charge Transport in LaAlO3/SrTiO3 with Time-Resolved Kelvin Probe Force Microscopy Surface Dynamics of Charge Transport in LaAlO3/SrTiO3 with Time-Resolved Kelvin Probe Force Microscopy AITranslate

Case Western Reserve University; Oak Ridge National Laboratory; Case Western Reserve University
AITranslate
Publisher: ACS
Share Citation Information Add to Favorites

    Scan to share on WeChat or Moments

Use WeChat scan.
Share with WeChat friends or Moments

Abstract AITranslate

Time-resolved Kelvin probe force microscopy (tr-KPFM) was used to map surface potential dynamics in LAO/STO under its critical thickness, where it acts as an insulator, as polarizing and depolarizing electric fields were applied to planar electrodes in ambient conditions. Two time constants, for polarization and relaxation (i.e., depolarization) each, were derived and were shown to be independent of the direction of electrical field, revealing the reproducibility and recovery of the surfaces. Ambient aging or recent electrical history did not change the surface kinetics as determined by tr-KPFM. During polarization, the faster time constant (∼3–6 s) is likely associated with the transport of H+ ions through the full length of the channel. The slower time constant (∼40–50 s), on the other hand, is observed across only half the channel width near the higher-potential─more positive─electrode, which is likely associated with an electrochemical reaction such as the dissociation of water. This slower time constant drops to ∼10–20 s toward the middle of the channel which could represent the transport of OH– ions. During relaxation, the fast time constant is consistent with polarization and is correlated to the same mechanism while the slower time constant is higher than it was during polarization and may represent the reabsorption of moisture from the atmosphere.

KeyWords AITranslate

trKPFM heterostructures surface kinetics adsorbed species time constants
No data

Basic Information:

DOI:https://doi.org/10.1021/acsaelm.1c00954

Chinese Library Classification Number:

Citation Information:

Time-resolved Kelvin probe force microscopy (tr-KPFM) was used to map surface potential dynamics in LAO/STO under its critical thickness, where it acts as an insulator, as polarizing and depolarizing electric fields were applied to planar electrodes in ambient conditions. Two time constants, for polarization and relaxation (i.e., depolarization) each, were derived and were shown to be independent of the direction of electrical field, revealing the reproducibility and recovery of the surfaces. Ambient aging or recent electrical history did not change the surface kinetics as determined by tr-KPFM. During polarization, the faster time constant (∼3–6 s) is likely associated with the transport of H+ ions through the full length of the channel. The slower time constant (∼40–50 s), on the other hand, is observed across only half the channel width near the higher-potential─more positive─electrode, which is likely associated with an electrochemical reaction such as the dissociation of water. This slower time constant drops to ∼10–20 s toward the middle of the channel which could represent the transport of OH– ions. During relaxation, the fast time constant is consistent with polarization and is correlated to the same mechanism while the slower time constant is higher than it was during polarization and may represent the reabsorption of moisture from the atmosphere.

quote

GB/T 7714-2015 [1] Hugh Smith, Liam Collins, Alp Sehirlioglu. ACS Applied Electronic Materials, 2022(4). DOI:10.1021/acsaelm.1c00954.
MLA [1] Hugh Smith, et al., ACS Applied Electronic Materials, no. 4, 2022, https://doi.org/10.1021/acsaelm.1c00954.
APA [1] Hugh Smith, Liam Collins, & Alp Sehirlioglu. (2022). ACS Applied Electronic Materials(4). https://doi.org/10.1021/acsaelm.1c00954
IEEE [1] Hugh Smith, Liam Collins, and Alp Sehirlioglu, ACS Applied Electronic Materials, no. 4, 2022, doi: 10.1021/acsaelm.1c00954. keywords: {trKPFM heterostructures surface kinetics adsorbed species time constants}