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Register a new userAbsence of field-induced charge-density wave states in (Per)$_2$Pt(mnt)$_2$
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Graf {it et al.} [Phys. Rev. Lett. {bf 93} 076406 (2004)] recently attributed features in the magnetic-field-dependent longitudinal resistance of (Per)$_2$Pt(mnt)$_2$ to a cascade of field-induced charge-density waves (FICDWs). Here we show that a quantitative magnetotransport analysis reveals orbital quantization to be absent, disproving the presence of FICDWs. Our data show that the conduction is instead dominated by the sliding CDW collective mode at low temperatures.
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A finite transfer integral $t_a$ orthogonal to the conducting chains of a highly one-dimensional metal gives rise to empty and filled bands that simulate an indirect-gap semiconductor upon formation of a commensurate charge-density-wave (CDW). In contrast to semiconductors such as Ge and Si with bandgaps $sim 1$ eV, the CDW system possesses an indirect gap with a greatly reduced energy scale, enabling moderate laboratory magnetic fields to have a major effect. The consequent variation of the thermodynamic gap with magnetic field due to Zeeman splitting and Landau quantization enables the electronic bandstructure parameters (transfer integrals, Fermi velocity) to be determined accurately. These parameters reveal the orbital quantization limit to be reached at $sim 20$ T in (Per)$_2M$(mnt)$_2$ salts, making them highly unlikely candidates for a recently-proposed cascade of field-induced charge-density wave states.
An inductive method is used to follow the magnetic field-dependent susceptibility of the coupled charge density wave (CDW) and spin-Peierls (SP) ordered state behavior in the dual chain organic conductor Perylene$_2$[Pt(mnt)$_2$]. In addition to the coexisting SP-CDW state phase below 8 K and 20 T, the measurements show that a second spin-gapped phase appears above 20 T that coincides with a field-induced insulating phase. The results support a strong coupling of the CDW and SP order parameters even in high magnetic fields, and provide new insight into the nature of the magnetic susceptibility of dual-chain spin and charge systems.
Substrate engineering provides an opportunity to modulate the physical properties of quantum materials in thin film form. Here we report that TiSe$_2$ thin films grown on TiO$_2$ have unexpectedly large electron doping that suppresses the charge density wave (CDW) order. This is dramatically different from either bulk single crystal TiSe$_2$ or TiSe$_2$ thin films on graphene. The epitaxial TiSe$_2$ thin films can be prepared on TiO$_2$ via molecular beam epitaxy (MBE) in two ways: by conventional co-deposition using selenium and titanium sources, and by evaporating only selenium on reconstructed TiO$_2$ surfaces. Both growth methods yield atomically flat thin films with similar physical properties. The electron doping and subsequent suppression of CDW order can be explained by selenium vacancies in the TiSe$_2$ film, which naturally occur when TiO$_2$ substrates are used. This is due to the stronger interfacial bonding that changes the ideal growth conditions. Our finding provides a way to tune the chemical potential of chalcogenide thin films via substrate selection and engineering.
We report on a thorough optical investigation of BaFe$_2$As$_2$ over a broad spectral range and as a function of temperature, focusing our attention on its spin-density-wave (SDW) phase transition at $T_{SDW}=135$ K. While BaFe$_2$As$_2$ remains metallic at all temperatures, we observe a depletion in the far infrared energy interval of the optical conductivity below $T_{SDW}$, ascribed to the formation of a pseudogap-like feature in the excitation spectrum. This is accompanied by the narrowing of the Drude term consistent with the $dc$ transport results and suggestive of suppression of scattering channels in the SDW state. About 20% of the spectral weight in the far infrared energy interval is affected by the SDW phase transition.
Understanding the complexities of electronic and magnetic ground states in solids is one of the main goals of solid-state physics. Materials with the canonical ThCr$_2$Si$_2$-type structure have proved particularly fruitful in this regards, as they exhibit a wide range of technologically advantageous physical properties described by many-body physics, including high-temperature superconductivity and heavy fermion behavior. Here, using high-resolution synchrotron X-ray diffraction and time-of-flight neutron scattering, we show that the isostructural mixed valence compound, KNi$_2$S$_2$, displays a number of highly unusual structural transitions, most notably the presence of charge density wave fluctuations that disappear on cooling. This behavior occurs without magnetic or charge order, in contrast to expectations based on all other known materials. Furthermore, the low-temperature electronic state of KNi$_2$S$_2$ is found to exhibit many characteristics of heavy-fermion behavior, including a heavy electron state ($m^*/m_e sim$ 24), with a negative coefficient of thermal expansion, and superconductivity below $T_c$ = 0.46(2) K. In the potassium nickel sulfide, these behaviors arise in the absence of localized magnetism, and instead appear to originate in proximity to charge order.
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