اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدAnisotropic magnetoresistance of charge-density wave in $o$-TaS$_3$
334
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We report the magnetoresistance of a charge-density wave (CDW) in $o$-TaS$_3$ whiskers at 4.2 K under a magnetic field up to 5.2 T. An anisotropic negative magnetoresistance is found in the nonlinear regime of current-voltage characteristics. The angle dependence of the magnetoresistance, studied by rotating the magnetic field upon the $c$-axis, exhibited a two-fold symmetry. The magnetoresistance amplitude exhibits maxima when the field is parallel to the $a$-axis, whereas it vanishes to the $b$-axis. The observed anisotropy may come from difference in interchain coupling of adjacent CDWs along the $a$- and $b$-axes. Comparison of the anisotropy to the scanning tunneling microscope image of CDWs allows us to provide a simple picture to explain the magnetoresistance in terms of delocalization of quantum interference of CDWs extending over the $b$-$c$ plane.
قيم البحث
اقرأ أيضاً
We studied the nonlocal transport of a quasi-one dimensional conductor $o$-TaS$_3$. Electric transport phenomena in charge density waves include the thermally-excited quasiparticles, and collective motion of charge density waves (CDW). In spite of it
s long-range correlation, the collective motion of a CDW does not extend far beyond the electrodes, where phase slippage breaks the correlation. We found that nonlocal voltages appeared in the CDW of $o$-TaS$_3$, both below and above the threshold field for CDW sliding. The temperature dependence of the nonlocal voltage suggests that the observed nonlocal voltage originates from the CDW even below the threshold field. Moreover, our observation of nonlocal voltages in both the pinned and sliding states reveals the existence of a carrier with long-range correlation, in addition to sliding CDWs and thermally-excited quasiparticles.
The transition metal dichalcogenide (TMD) $1T$-TaS$_{2}$ exhibits a rich set of charge density wave (CDW) orders. Recent investigations suggested that using light or electric field can manipulate the commensurate (C) CDW ground state. Such manipulati
ons are considered to be determined by the charge carrier doping. Here we simulate by first-principles calculations the carrier doping effect on CCDW in $1T$-TaS$_{2}$. We investigate the charge doping effects on the electronic structures and phonon instabilities of $1T$ structure and analyze the doping induced energy and distortion ratio variations in CCDW structure. We found that both in bulk and monolayer $1T$-TaS$_{2}$, CCDW is stable upon electron doping, while hole doping can significantly suppress the CCDW, implying different mechanisms of such reported manipulations. Light or positive perpendicular electric field induced hole doping increases the energy of CCDW, so that the system transforms to NCCDW or similar metastable state. On the other hand, even the CCDW distortion is more stable upon in-plain electric field induced electron injection, some accompanied effects can drive the system to cross over the energy barrier from CCDW to nearly commensurate (NC) CDW or similar metastable state. We also estimate that hole doping can introduce potential superconductivity with $T_{c}$ of $6sim7$ K. Controllable switching of different states such as CCDW/Mott insulating state, metallic state, and even the superconducting state can be realized in $1T$-TaS$_{2}$, which makes the novel material have very promising applications in the future electronic devices.
We study the coupled charge-lattice dynamics in the commensurate charge density wave (CDW) phase of the layered compound 1T-TaS$_{2}$ driven by an ultrashort laser pulse. For describing its electronic structure, we employ a tight-binding model of pre
vious studies including the effects of lattice distortion associated with the CDW order. We further add on-site Coulomb interactions and reproduce an energy gap at the Fermi level within a mean-field analysis. On the basis of coupled equations of motion for electrons and the lattice distortion, we numerically study their dynamics driven by an ultrashort laser pulse. We find that the CDW order decreases and even disappears during the laser irradiation while the lattice distortion is almost frozen. We also find that the lattice motion sets in on a longer time scale and causes a further decrease in the CDW order even after the laser irradiation.
We present an angle-resolved photoemission (ARPES) study on the layered transition-metal dichalcogenide 1{em T}-TaS$_{1.2}$Se$_{0.8}$ in the metallic commensurate charge-density-wave (CDW) phase. A model calculation of the spectral function captures
the main features of the ARPES spectra well qualitatively, that is, the gross splits of unreconstructed band structure in the absence of the CDW superlattice. The observed enhancement of the size of the gap between the lower and middle fragments of the Ta {em 5d} band along the $Gamma$M line by cooling is interpreted in terms of the increase in the CDW-related potential.
We report an in-depth Angle Resolved Photoemission Spectroscopy (ARPES) study on $2H$-TaS$_2$, a canonical incommensurate Charge Density Wave (CDW) system. This study demonstrates that just as in related incommensurate CDW systems, $2H$-TaSe$_2$ and
$2H$-NbSe$_2$, the energy gap ($Delta_{text{cdw}},$) of $2H$-TaS$_2$ is localized along the K-centered Fermi surface barrels and is particle-hole asymmetric. The persistence of $Delta_{text{cdw}},$ even at temperatures higher than the CDW transition temperature $it{T}_{text{cdw}},$ in $2H$-TaS$_2$, reflects the similar pseudogap (PG) behavior observed previously in $2H$-TaSe$_2$ and $2H$-NbSe$_2$. However, in sharp contrast to $2H$-NbSe$_2$, where $Delta_{text{cdw}},$ is non-zero only in the vicinity of a few hot spots on the inner K-centered Fermi surface barrels, $Delta_{text{cdw}},$ in $2H$-TaS$_2$ is non-zero along the entirety of both K-centered Fermi surface barrels. Based on a tight-binding model, we attribute this dichotomy in the momentum dependence and the Fermi surface specificity of $Delta_{text{cdw}},$ between otherwise similar CDW compounds to the different orbital orientations of their electronic states that are involved in CDW pairing. Our results suggest that the orbital selectivity plays a critical role in the description of incommensurate CDW materials.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
