Pregled bibliografske jedinice broj: 91744
Complex low-frequency dielectric relaxation of the charge-density wave state in the (2, 5(OCH3)2DCNQI)2Li
Complex low-frequency dielectric relaxation of the charge-density wave state in the (2, 5(OCH3)2DCNQI)2Li // European physical journal B : condensed matter physics, 22 (2001), 3; 335-341 doi:10.1007/s100510170111 (međunarodna recenzija, članak, znanstveni)
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Naslov
Complex low-frequency dielectric relaxation of the charge-density wave state in the (2, 5(OCH3)2DCNQI)2Li
Autori
Pinterić, Marko ; Vuletić, Tomislav ; Tomić, Silvia ; von Schütz, Ulrich Jost
Izvornik
European physical journal B : condensed matter physics (1434-6028) 22
(2001), 3;
335-341
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
collective modes; low dimensional conductors; charge-density wave systems; dielectric loss and relaxation
Sažetak
We report a detailed characterization of an unique 2- and 4-fold commensurate charge density wave (CDW) state in single crystals of the organic conductor (2, 5(OCH_3)_2 DCNQI)_2 Li by means of low-frequency (0.1~Hz--1~MHz) dielectric spectroscopy. We show that in addition to the narrow Debye-like relaxation mode of strength \Delta\epsilon \approx 10^7 with Arrhenius-like resistive decay, associated with long wavelength phason excitations, a new mode of weaker strength \Delta\epsilon \approx 10^6 appears below 40K and broadens with decrease in temperature. Below 25K the mean relaxation time of the new mode saturates, whereas the Debye mode continues gradual slowing down with weaker temperature dependence, again similar to the DC conductivity. We attribute the new process to short wavelength CDW excitations that become dominant once the free carrier density is substantially reduced at low temperatures.
Izvorni jezik
Engleski
Znanstvena područja
Fizika
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus