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Register a new userEnhanced Magnetism & Time - Stable Remanence at the Interface of Hematite and Carbon Nanotubes
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The interface of two dissimilar materials is well known for surprises in condensed matter, and provides avenues for rich physics as well as seeds for future technological advancements. We present some exciting magnetization (M) and remnant magnetization ($mu$) results, which conclusively arise at the interface of two highly functional materials, namely the graphitic shells of a carbon nanotube (CNT) and $alpha$-Fe$_2$O$_3$, a Dzyaloshinskii-Moriya Interaction (DMI) driven weak ferromagnet (WFM) and piezomagnet (PzM). We show that the encapsulation inside CNT leads to a very significant enhancement in M and correspondingly in $mu$, a time- stable part of the remanence, exclusive to the WFM phase. Up to 70% of in-field magnetization is retained in the form of $mu$ at the room temperature. Lattice parameter of CNT around the Morin transition of the encapsulate exhibits a clear anomaly, confirming the novel interface effects. Control experiments on bare $alpha$-Fe$_2$O$_3$ nanowires bring into fore that the weak ferromagnets such as $alpha$-Fe$_2$O$_3$ as are not as weak, as far as their remanence and its stability with time is concerned, and encapsulation inside CNT leads to a substantial enhancement in these functionalities.
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We have recently established that a number of Dzyaloshinskii-Moriya interaction driven canted antiferromagnets or weak ferrromagnets (WFM) including hematite exhibit an ultra-slow magnetization relaxation phenomenon, leading to the observation of a time-stable remanence (Phys. Rev. B 96, 104422 (2017)). In this work, our endeavor is to optimize the magnitude of this time-stable remanence for the hematite crystallites, as a function of shape size and morphology. A substantial enhancement in the magnitude of this unique remanence is observed in porous hematite, consisting of ultra-small nano particles, as compared to crystallites grown in regular morphology, such as cuboids or hexagonal plates. This time-stable remanence exhibits a peak-like pattern with magnetic field, which is significantly sharper in porous sample. The extent and the magnitude of the spin canting associated with the WFM phase can be best gauged by the presence of this remanence and its unusual magnetic field dependence. Temperature variation of lattice parameters bring out correlations between strain effects that alter the bond length and bond angle associated with primary super exchange paths, which in-turn systematically alter the magnitude of the time-stable remanence. This study provides insights regarding a long standing problems of anomalies in the magnitude of magnetization on repeated cooling in case of hematite. Our data caps on these anomalies, which we argue, arise due to spontaneous spin canting associated with WFM phase. Our results also elucidate on why thermal cycling protocols during bulk magnetization measurements are even more crucial for hematite which exhibits both canted as well as pure antiferromgnetic phase.
We investigate the electronic structure of carbon nanotubes functionalized by adsorbates anchored with single C-C covalent bonds. We find that, despite the particular adsorbate, a spin moment with a universal value of 1.0 $mu_B$ per molecule is induced at low coverage. Therefore, we propose a mechanism of bonding-induced magnetism at the carbon surface. The adsorption of a single molecule creates a dispersionless defect state at the Fermi energy, which is mainly localized in the carbon wall and presents a small contribution from the adsorbate. This universal spin moment is fairly independent of the coverage as long as all the molecules occupy the same graphenic sublattice. The magnetic coupling between adsorbates is also studied and reveals a key dependence on the graphenic sublattice adsorption site.
We report the observation of an intriguing behaviour in the transport properties of nanodevices operating in a regime between the Fabry-Perot and the Kondo limits. Using ultra-high quality nanotube devices, we study how the conductance oscillates when sweeping the gate voltage. Surprisingly, we observe a four-fold enhancement of the oscillation period upon decreasing temperature, signaling a crossover from single-electron tunneling to Fabry-Perot interference. These results suggest that the Fabry-Perot interference occurs in a regime where electrons are correlated. The link between the measured correlated Fabry-Perot oscillations and the SU(4) Kondo effect is discussed.
The dynamical conductance of electrically contacted single-walled carbon nanotubes is measured from dc to 10 GHz as a function of source-drain voltage in both the low-field and high-field limits. The ac conductance of the nanotube itself is found to be equal to the dc conductance over the frequency range studied for tubes in both the ballistic and diffusive limit. This clearly demonstrates that nanotubes can carry high-frequency currents at least as well as dc currents over a wide range of operating conditions. Although a detailed theoretical explanation is still lacking, we present a phenomenological model of the ac impedance of a carbon nanotube in the presence of scattering that is consistent with these results.
In-situ Raman experiments together with transport measurements have been carried out on carbon nanotubes as a function of gate voltage. In metallic tubes, a large increase in the Raman frequency of the $G^-$ band, accompanied by a substantial decrease of its line-width, is observed with electron or hole doping. In addition, we see an increase in Raman frequency of the $G^+$ band in semiconducting tubes. These results are quantitatively explained using ab-initio calculations that take into account effects beyond the adiabatic approximation. Our results imply that Raman spectroscopy can be used as an accurate measure of the doping of both metallic and semiconducting nanotubes.
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