Low temperature photoluminescence (PL) and photoluminescence excitation (PLE) spectroscopy of high purity ErSc(2)N@C(80) and Er(2)ScN@C(80) fullerenes reveal at least two metastable configurations of the Er(3+) ion within the cage, consistent with previous observations from x-ray diffraction. Using PLE measurements at a number of different emission wavelengths we have characterized the ground state, (4)I(152), and the first excited state, (4)I(132), of the various Er(3+) configurations and their crystal-field splitting. We present detailed energy level diagrams for the ground and excited states of the two dominant configurations of ErSc(2)N@C(80) and Er(2)ScN@C(80).
While the anomalous Hall effect can manifest even without an external magnetic field, time reversal symmetry is nonetheless still broken by the internal magnetization of the sample. Recently, it has been shown that certain materials without an inversion center allow for a nonlinear type of anomalous Hall effect whilst retaining time reversal symmetry. The effect may arise from either Berry curvature or through various asymmetric scattering mechanisms. Here, we report the observation of an extremely large c-axis nonlinear anomalous Hall effect in the non-centrosymmetric Td phase of MoTe2 and WTe2 without intrinsic magnetic order. We find that the effect is dominated by skew-scattering at higher temperatures combined with another scattering process active at low temperatures. Application of higher bias yields an extremely large Hall ratio of E⊥/E|| = 2.47 and corresponding anomalous Hall conductivity of order 8 × 107 S/m.
Motivated by the possibility of observing photoluminescence and electron paramagnetic resonance from the same species located within a fullerene molecule, we initiated an EPR study of Er3+ in ErSc2N@C80. Two orientations of the ErSc2N rotor within the C80 fullerene are observed in EPR, consistent with earlier studies using photoluminescence excitation (PLE) spectroscopy. For some crystal field orientations, electron spin relaxation is driven by an Orbach process via the first excited electronic state of the 4I(15/2) multiplet. We observe a change in the relative populations of the two ErSc2N configurations upon the application of 532 nm illumination, and are thus able to switch the majority cage symmetry. This photoisomerization, observable by both EPR and PLE, is metastable, lasting many hours at 20 K.
Here we report systematic studies on the epitaxial growth and properties of Zn1−xVxO[x=0.001-0.2] thin films deposited onto sapphire c-plane single crystals. The thin films were deposited using pulsed laser deposition technique and were found to be epitaxial in nature. X-ray diffraction and high resolution transmission electron microscopy were employed to study the epitaxial relations of Zn1−xVxO with the sapphire substrate and electron energy loss spectroscopy was used to establish the bonding characteristics and oxidation states of vanadium inside the ZnO host. The main emphasis is on the magnetic properties of this system taking into consideration the phase purity and microstructural characteristics of these films. Our results show that the Zn1−xVxO system, with V in zinc substitutional sites, does not exhibit any signature of ferromagnetism, both at room temperature as well as at lower temperatures down to 10 K.
We use both classical magnetotransport and quantum oscillation measurements to study the thickness evolution of the extremely large magnetoresistance (XMR) material and type-II Weyl semimetal candidate, -MoTe2, protected from oxidation. We find that the magnetoresistance is systematically suppressed with reduced thickness. This occurs concomitantly with both a decrease in carrier mobility and increase in electron-hole imbalance. We model the two effects separately and conclude that the XMR effect is more sensitive to the former.
Main text:Among the layered transition metal dichalcogenides (TMDCs), MoTe2 is a unique member that crystallizes in both semiconducting 2H and semimetallic 1T-type structures, making it an appealing candidate for novel phase-changing electronics [1]. It has already been demonstrated, for example, that transitions between the two can be controlled by strain, alloying, and electrostatic gating [2][3][4][5][6]. The semimetal polytype itself is interesting and exhibits different phases. First, true 1T coordination is unstable as in-plane bond distortions dimerize the Mo atoms along the b-axis. Two stacking configurations of these distorted layers along the c-axis give rise to distinct three-dimensional (3D) structures: the centrosymmetric (or 1T') phase at high temperature (above ~250K) and the noncentrosymmetric (or Td) phase at low temperature, with the difference being only a ~4 ∘ tilt in the unit cell. The latter structure notably hosts type-II Weyl nodes [7-13] and exhibits extremely large magnetoresistance (XMR) below ~20K [14]. XMR materials may be useful for spintronics and sensing applications. While both -MoTe2 and -WTe2, a structurally similar compound, have been shown to demonstrate XMR [14,15], its origin in the former is under debate. Transport studies have attributed the cause to a close compensation of electron and hole concentrations at low temperature for both materials [16-19]; however, angle-resolved photoemission experiments report that MoTe2 remains uncompensated at all temperatures [20], in contrast to WTe2 [21]. One can directly test the effect of charge (un)compensation on XMR in MoTe2 by changing the relative carrier concentrations, but this is generally difficult to do in bulk systems without introducing unwanted disorder.Recently, several of the authors have shown that the phase is realized in thin MoTe2
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