scholarly journals Colossal variations in the thermopower and n–p conductivity switching in topological tellurides under pressure

2020 ◽  
Vol 128 (24) ◽  
pp. 245902
Author(s):  
Natalia V. Morozova ◽  
Igor V. Korobeinikov ◽  
Kirill V. Kurochka ◽  
Sergey V. Ovsyannikov
2021 ◽  
Vol 118 (4) ◽  
pp. 042409
Author(s):  
Hiroyasu Nakayama ◽  
Bin Xu ◽  
Sotaro Iwamoto ◽  
Kaoru Yamamoto ◽  
Ryo Iguchi ◽  
...  

2010 ◽  
Vol 97 (26) ◽  
pp. 262114 ◽  
Author(s):  
M. G. Vergniory ◽  
J. M. Granadino-Roldan ◽  
A. Garcia-Lekue ◽  
Lin-Wang Wang

2011 ◽  
Vol 2011 ◽  
pp. 1-9 ◽  
Author(s):  
J. A. Avila-Niño ◽  
A. O. Sustaita ◽  
M. Reyes-Reyes ◽  
R. López-Sandoval

The effect of thickness variation on the memory behavior of the polymethylmethacrylate-(PMMA)-based devices has been investigated. The PMMA film thicknesses have been varied between 5 to 300 nm, and we have found that the film thickness determines the type of behavior: ohmic, write-once-read-many-times (WORM) memory with two ON states, WORM memory with a negative differential resistance (NDR) region, and WORM memory without NDR region. The fact that similar results were obtained using different solvents to dilute PMMA (chlorobenzene, chloroform, and dimethyl sulfoxide), as well as using an other insulating polymer such as polystyrene (PS), leads to the conclusion that the phenomenon of memory depends on the aluminum electrodes, organic film thickness, and the compliance current used during the electroformation whereas the type of organic layer (PMMA or PS) has minor influence. From here, we conclude that the conductivity switching of the insulator organic film is due to the injection of aluminum particles into the film during the first voltage cycle.


2016 ◽  
Vol 28 (47) ◽  
pp. 475501 ◽  
Author(s):  
LiDong Dai ◽  
Lei Wu ◽  
HePing Li ◽  
HaiYing Hu ◽  
YuKai Zhuang ◽  
...  

2012 ◽  
Vol 162 (13-14) ◽  
pp. 1059-1064 ◽  
Author(s):  
Yang Liu ◽  
Shujun Lv ◽  
Liang Li ◽  
Songmin Shang

1976 ◽  
Vol 36 (2) ◽  
pp. 475-478 ◽  
Author(s):  
M. Peršin ◽  
D. Kunstelj ◽  
A. Peršin ◽  
H. Zorc

2019 ◽  
Vol 116 (13) ◽  
pp. 5973-5978 ◽  
Author(s):  
Jungwoo Shin ◽  
Jaeuk Sung ◽  
Minjee Kang ◽  
Xu Xie ◽  
Byeongdu Lee ◽  
...  

Materials that can be switched between low and high thermal conductivity states would advance the control and conversion of thermal energy. Employing in situ time-domain thermoreflectance (TDTR) and in situ synchrotron X-ray scattering, we report a reversible, light-responsive azobenzene polymer that switches between high (0.35 W m−1K−1) and low thermal conductivity (0.10 W m−1K−1) states. This threefold change in the thermal conductivity is achieved by modulation of chain alignment resulted from the conformational transition between planar (trans) and nonplanar (cis) azobenzene groups under UV and green light illumination. This conformational transition leads to changes in the π-π stacking geometry and drives the crystal-to-liquid transition, which is fully reversible and occurs on a time scale of tens of seconds at room temperature. This result demonstrates an effective control of the thermophysical properties of polymers by modulating interchain π-π networks by light.


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