TY  - JOUR
A1  - Miyamoto, Ko-ichiro
A1  - Bing, Yu
A1  - Wagner, Torsten
A1  - Yoshinobu, Tatsuo
A1  - Schöning, Michael Josef
T1  - Visualization of Defects on a Cultured Cell Layer by Utilizing Chemical Imaging Sensor
JF  - Procedia Engineering
N2  - The chemical imaging sensor is a field-effect sensor which is able to visualize both the distribution of ions (in LAPS mode) and the distribution of impedance (in SPIM mode) inthe sample. In this study, a novel wound-healing assay is proposed, in which the chemical imaging sensor operated in SPIM mode is applied to monitor the defect of a cell layer brought into proximity of the sensing surface.A reduced impedance inside the defect, which was artificially formed ina cell layer, was successfully visualized in a photocurrent image.
Y1  - 2015
U6  - https://doi.org/10.1016/j.proeng.2015.08.806
SN  - 1877-7058
N1  - Part of special issue "Eurosensors 2015"
VL  - 120
SP  - 936
EP  - 939
PB  - Elsevier
CY  - Amsterdam
ER  - 
TY  - JOUR
A1  - Miyamoto, Ko-ichiro
A1  - Yu, Bing
A1  - Isoda, Hiroko
A1  - Wagner, Torsten
A1  - Schöning, Michael Josef
A1  - Yoshinobu, Tatsuo
T1  - Visualization of the recovery process of defects in a cultured cell layer by chemical imaging sensor
JF  - Sensors and Actuators B: Chemical
N2  - The chemical imaging sensor is a field-effect sensor which is able to visualize both the distribution of ions (in LAPS mode) and the distribution of impedance (in SPIM mode) in the sample. In this study, a novel cell assay is proposed, in which the chemical imaging sensor operated in SPIM mode is applied to monitor the recovery of defects in a cell layer brought into proximity of the sensing surface. A reduced impedance at a defect formed artificially in a cell layer was successfully visualized in a photocurrent image. The cell layer was cultured over two weeks, during which the temporal change of the photocurrent distribution corresponding to the recovery of the defect was observed.
Y1  - 2016
U6  - https://doi.org/10.1016/j.snb.2016.04.018
SN  - 0925-4005
VL  - 236
SP  - 965
EP  - 969
PB  - Elsevier
CY  - Amsterdam
ER  - 
TY  - JOUR
A1  - Windmüller, Anna
A1  - Schaps, Kristian
A1  - Zantis, Frederik
A1  - Domgans, Anna
A1  - Taklu, Bereket Woldegbreal
A1  - Yang, Tingting
A1  - Tsai, Chih-Long
A1  - Schierholz, Roland
A1  - Yu, Shicheng
A1  - Kungl, Hans
A1  - Tempel, Hermann
A1  - Dunin-Borkowski, Rafal E.
A1  - Hüning, Felix
A1  - Hwang, Bing Joe
A1  - Eichel, Rüdiger-A.
T1  - Electrochemical activation of LiGaO2: implications for ga-doped garnet solid electrolytes in li-metal batteries
JF  - ACS Applied Materials & Interfaces
N2  - Ga-doped Li7La3Zr2O12 garnet solid electrolytes exhibit the highest Li-ion conductivities among the oxide-type garnet-structured solid electrolytes, but instabilities toward Li metal hamper their practical application. The instabilities have been assigned to direct chemical reactions between LiGaO2 coexisting phases and Li metal by several groups previously. Yet, the understanding of the role of LiGaO2 in the electrochemical cell and its electrochemical properties is still lacking. Here, we are investigating the electrochemical properties of LiGaO2 through electrochemical tests in galvanostatic cells versus Li metal and complementary ex situ studies via confocal Raman microscopy, quantitative phase analysis based on powder X-ray diffraction, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and electron energy loss spectroscopy. The results demonstrate considerable and surprising electrochemical activity, with high reversibility. A three-stage reaction mechanism is derived, including reversible electrochemical reactions that lead to the formation of highly electronically conducting products. The results have considerable implications for the use of Ga-doped Li7La3Zr2O12 electrolytes in all-solid-state Li-metal battery applications and raise the need for advanced materials engineering to realize Ga-doped Li7La3Zr2O12for practical use.
KW  - LiGaO2
KW  - garnet solid electrolyte
KW  - ga-doping
KW  - Li7La3Zr2O12
KW  - solid-state battery
Y1  - 2024
U6  - https://doi.org/10.1021/acsami.4c03729
SN  - 39181–3919
VL  - 16
IS  - 30
PB  - ACS Publications
CY  - Washington, DC
ER  -