scholarly journals Dipolar spin relaxation of divacancy qubits in silicon carbide

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Oscar Bulancea-Lindvall ◽  
Nguyen T. Son ◽  
Igor A. Abrikosov ◽  
Viktor Ivády

AbstractDivacancy spins implement qubits with outstanding characteristics and capabilities in an industrial semiconductor host. On the other hand, there are still numerous open questions about the physics of these important defects, for instance, spin relaxation has not been thoroughly studied yet. Here, we carry out a theoretical study on environmental spin-induced spin relaxation processes of divacancy qubits in the 4H polytype of silicon carbide (4H-SiC). We reveal all the relevant magnetic field values where the longitudinal spin relaxation time T1 drops resonantly due to the coupling to either nuclear spins or electron spins. We quantitatively analyze the dependence of the T1 time on the concentration of point defect spins and the applied magnetic field and provide an analytical expression. We demonstrate that dipolar spin relaxation plays a significant role both in as-grown and ion-implanted samples and it often limits the coherence time of divacancy qubits in 4H-SiC.

2015 ◽  
Vol 233-234 ◽  
pp. 149-152
Author(s):  
Victor Pavlov ◽  
Valerii Gridnev ◽  
Roman Pisarev ◽  
Martin Pohl ◽  
Ilya Akimov ◽  
...  

Transient optical anisotropy in the hexagonal manganite YMnO3excited by linearly and circularly polarized laser pulses has been observed. The photo-induced anisotropy was investigated by the pump-probe technique based on a femtosecond Ti:sapphire laser generating optical pulses at the photon energy of 1.55 eV. Temporal and spectral dependencies of the photo-induced optical rotation and ellipticity were analyzed by a theoretical model considering ultrafast population and relaxation processes near the interband transitions from the hybridized O2−(2p)-Mn3+(3d) (Γ1) to the Mn3+(3d3z2−r2) (Γ5) states at photon energies of the laser excitation. Very short relaxation time of ~10 fs, which is the Raman coherence time between the excited Γ5|x> and Γ5|y> states, has been determined. It is found that this coherence time is much shorter than a charge relaxation time of ~500 fs between the Γ5|x,y> and Γ1|g> states for the interband electronic transition Γ1→Γ5.


1999 ◽  
Vol 13 (14n16) ◽  
pp. 1791-1797 ◽  
Author(s):  
S. Cutillas ◽  
G. Bossis ◽  
E. Lemaire ◽  
A. Meunier ◽  
A. Cebers

We present here the study of field induced phase separation in E.R. and M.R. fluids. Two thermodynamic models — one for the formation of chais of particles and the other for phase separation are presented and compared with experimental results obtained with two kinds of suspensions. One was made of silica particles in silicone oil and the other was made of magnetic polystyrene particles in water. In the presence of a flow the phase separation occurs with the dense phase forming a regular pattern of stripes. The dependence of the period of these stripes on the intensity of the magnetic field is well reproduced by the same kind of thermodynamic model if we add the effect of normal stresses induced by the shear flow.


2012 ◽  
Vol 44 (1-2) ◽  
pp. 23-39 ◽  
Author(s):  
Andrey N. Pravdivtsev ◽  
Konstantin L. Ivanov ◽  
Robert Kaptein ◽  
Alexandra V. Yurkovskaya

1961 ◽  
Vol 39 (6) ◽  
pp. 870-880 ◽  
Author(s):  
G. T. Needler ◽  
W. Opechowski

The Schwinger formula for the relaxation time T1 of nuclear spins in hydrogen gas is valid only for sufficiently low temperatures. In this paper an approximate theory of T1 is developed valid for any temperature. An explicit expression is given for T1 valid for temperatures up to room temperature; this expression reduces to the Schwinger formula for sufficiently low temperatures.


Author(s):  
Sridhar Patibandla ◽  
Bhargava Kanchibotla ◽  
Sandipan Pramanik ◽  
Supriyo Bandyopadhyay ◽  
Marc Cahay

We have measured the longitudinal (T1) and transverse (T2) spin relaxation times in the organic semiconductor tris(8-hydroxyquinolinolato aluminum)—also known as Alq3—at different temperatures. These measurements shed some light on the spin relaxation mechanisms in the organic. The two most likely mechanisms affecting T1 are hyperfine interactions between carrier and nuclear spins, and the Elliott-Yafet mode. On the other hand, the dominant mechanism affecting T2 of delocalized electrons in Alq3 remains uncertain, but for localized electrons (bound to defect or impurity sites), the dominant mechanism is most likely spin-phonon coupling.


1986 ◽  
Vol 64 (6) ◽  
pp. 733-735 ◽  
Author(s):  
J. S. Blicharski

The effective relaxation time T2e is calculated in the weak-collision case, for identical nuclear spins in the presence of a Mansfield–Ware-4 multipulse sequence. The dipole–dipole, quadrupole, and spin-rotational interactions are taken into account.


2009 ◽  
Vol 23 (12n13) ◽  
pp. 2585-2586
Author(s):  
JUNSAKU NITTA

The spin dynamics in solid state systems is governed by the competition between spin-orbit interaction (SOI) and the Zeeman effect. The SOI couples orbital motion of electron spins with an electric field. The Zeeman effect lifts the spin degeneracy in a magnetic field. In InGaAs -based 2DEGs, it is known that the Rashba SOI energy E SOI can be controlled by an electric field applied on the gate electrode.1 In the presence of SOI, weak localization (WL) due to time reversal symmetric interference changes to weak anti-localization (WAL). We have found crossover from WL to WAL by applying the gate voltage in InGaAs 2DEGs. Applying an in-plane magnetic field to the 2DEG does not affect the orbital motion of the electrons, but only modifies the Zeeman spin splitting energy E Z . This allows tuning the ratio between E SOI and E Z very accurately. We have studied how the interplay between SOI and Zeeman coupling affects the electron transport and the spin dynamics in InGaAs -based 2DEGs. From the quantitative analysis of the magnetoconductance, measured in the presence of an in-plane magnetic field, we conclude that this interplay results in a spin-induced breaking of time reversal symmetry (TRS) and in an enhancement of the spin relaxation time. Both effects are due to a partial alignment of the electron spin along the applied magnetic field, and are found to be in excellent agreement with recent theoretical predictions.2 We find that the electron dephasing time saturates when E Z becomes comparable to E SOI . Moreover, we show that the spin-induced electron dephasing time is a universal function of the ratio E Z /E SOI within the experimental accuracy, i.e. it is independent of any details of the quantum well.3 This universal behavior is explained by the recent theory.4 The suppression of WAL is observed by applying in-plane magnetic field because of the enhancement of the spin relaxation time, and this suppression also appears in narrow InGaAs wires since the effective magnetic field direction is confined by wires. In gate fitted narrow wires, the large enhancement of spin relaxation time is obtained when the Rashba SOI is decreased. The spin relaxation time is more than one order longer than that of 2DEG case. This enhancement suggests that the Rashba SOI strength approaches the Dresselhaus SOI strength. We have numerically investigated the angular dependence of in-plane magnetoconductance in disordered wires with both Rashba and Dresselhaus SOIs. A new method is proposed to determine the relative strength of Rashba and Dresselhaus SOI from transport measurements without the need of fitting parameters.5 This in-plane magnetic field measurement provides fruitful information on spin related transport. Note from Publisher: This article contains the abstract only.


Author(s):  
Sridhar Patibandla ◽  
Bhargava Kanchibotla ◽  
Sandipan Pramanik ◽  
Supriyo Bandyopadhyay ◽  
Marc Cahay

We have measured the longitudinal (T1) and transverse (T2) spin relaxation times in the organic semiconductor tris(8-hydroxyquinolinolato aluminum) - also known as Alq3 - at different temperatures and under different electric fields driving current. These measurements shed some light on the spin relaxation mechanisms in the organic. The two most likely mechanisms affecting T1 are hyperfine interactions between carrier and nuclear spins, and the Elliott-Yafet mode. On the other hand, the dominant mechanism affecting T2 of delocalized electrons in Alq3 remains uncertain, but for localized electrons (bound to defect or impurity sites), the dominant mechanism is most likely spin-phonon coupling.


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