Electric field effects in superconducting YBa2Cu3O7−xthin films using field‐effect transistor structures

1995 ◽  
Vol 77 (2) ◽  
pp. 761-764 ◽  
Author(s):  
E. H. Taheri ◽  
J. W. Cochrane ◽  
G. J. Russell
Keyword(s):  
Electric Field ◽  
Field Effect ◽  
Field Effect Transistor ◽  
Electric Field Effects ◽  
Field Effects ◽  
Effect Transistor

Partial Dissolution of Charge Order Phase Observed in -(BEDT-TTF)2PF6 Single Crystal Field Effect Transistor

2016 ◽  
Vol 16 (4) ◽  
pp. 3267-3272
Author(s):  
Masatoshi Sakai ◽  
Norifumi Moritoshi ◽  
Shigekazu Kuniyoshi ◽  
Hiroshi Yamauchi ◽  
Kazuhiro Kudo ◽  
...  
Keyword(s):  
Electric Field ◽  
Single Crystal ◽  
Temperature Dependence ◽  
Crystal Field ◽  
Field Effect ◽  
Field Effect Transistor ◽  
Electrical Conductance ◽  
Charge Order ◽  
Crystal Field Effect ◽  
Effect Transistor

The effect of an applied gate electric field on the charge-order phase in β-(BEDT-TTF)2PF6 single-crystal field-effect transistor structure was observed at around room temperature by technical improvement with respect to sample preparation and electrical measurements. A relatively slight but systematic increase of the electrical conductance induced by the applied gate electric field and its temperature dependence was observed at around the metal-insulator transition temperature (TMI). The temperature dependence of the modulated electrical conductance demonstrated that TMI was shifted toward the lower side by application of a gate electric field, which corresponds to partial dissolution of the charge-order phase. The thickness of the partially dissolved charge order region was estimated to be several score times larger than the charge accumulation region.

Substituent-induced 1H chemical shifts for 4-substituted (2, 2-dichlorocyclopropyl)benzenes: further evidence for intramolecular electric field effects on 1H chemical shifts

1977 ◽  
Vol 55 (3) ◽  
pp. 530-535 ◽  
Author(s):  
Robert H. Kohler ◽  
William F. Reynolds
Keyword(s):  
Electric Field ◽  
Field Effect ◽  
Ring Current ◽  
Chemical Shifts ◽  
Basic Pattern ◽  
Electric Field Effects ◽  
Field Effects ◽  
The Individual ◽  
Induced Changes ◽  
Proton Chemical Shifts

Correlations of cyclopropyl proton chemical shifts for 4-substituted (2,2-dichlorocyclopropyl)-benzenes with σI and σR0 provide evidence that these chemical shifts reflect direct field effects and weak phenyl–cyclopropyl conjugative interactions. Corrections for variable ring current effects due to substituent-induced changes in conformation improve the individual correlations but do not alter the basic pattern of results. Correlation of the β cyclopropyl 1H chemical shift difference with σI with calculated hydrogen electron densities, and with calculated electric field components provides further strong evidence for a field effect on 1H chemical shifts.

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