scholarly journals The Underlying Spin−Orbit Coupling Structure of Intervalence Charge Transfer Bands in Dinuclear Polypyridyl Complexes of Ruthenium and Osmium

2006 ◽  
Vol 45 (11) ◽  
pp. 4576-4576
Author(s):  
D. M. D'Alessandro ◽  
P. H. Dinolfo ◽  
M. S. Davies ◽  
J. T. Hupp ◽  
F. R. Keene
Keyword(s):  
Charge Transfer ◽  
Orbit Coupling ◽  
Spin Orbit Coupling ◽  
Spin Orbit ◽  
Polypyridyl Complexes ◽  
Coupling Structure ◽  
Intervalence Charge Transfer

Underlying Spin−Orbit Coupling Structure of Intervalence Charge Transfer Bands in Dinuclear Polypyridyl Complexes of Ruthenium and Osmium

2006 ◽  
Vol 45 (8) ◽  
pp. 3261-3274 ◽  
Author(s):  
Deanna M. D'Alessandro ◽  
Peter H. Dinolfo ◽  
Murray S. Davies ◽  
Joseph T. Hupp ◽  
F. Richard Keene
Keyword(s):  
Charge Transfer ◽  
Orbit Coupling ◽  
Spin Orbit Coupling ◽  
Spin Orbit ◽  
Polypyridyl Complexes ◽  
Coupling Structure ◽  
Intervalence Charge Transfer

The suppression of spin–orbit coupling effect by the ZnO layer of La0.7Sr0.3MnO3/ZnO heterostructures grown on (001) oriented Si restores the negative magnetoresistance

Nanoscale ◽  
2021 ◽  
Author(s):  
Bibekananda Das ◽  
Prahallad Padhan
Keyword(s):  
Charge Transfer ◽  
Coupling Effect ◽  
Orbit Coupling ◽  
Negative Magnetoresistance ◽  
Magnetic Scattering ◽  
Spin Orbit Coupling ◽  
Spin Orbit ◽  
Interfacial Charge Transfer ◽  
Positive Magnetoresistance ◽  
Interfacial Charge

In Si–La0.7Sr0.3MnO3, the interfacial charge transfer driven strong localized antiferromagnetic and spin–orbit couplings favor positive magnetoresistance, which is suppressed by strong magnetic scattering induced by the top ZnO layer results in negative magnetoresistance.

Enhanced blue TADF in D-A-D type naphthyridine derivative with asymmetric carbazole-donor motif

2022 ◽  
Author(s):  
Dovydas Banevičius ◽  
Gediminas Kreiza ◽  
Rokas Klioštoraitis ◽  
Saulius Jursenas ◽  
Tomas Javorskis ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Triplet State ◽  
Orbit Coupling ◽  
Spin Orbit Coupling ◽  
Spin Orbit ◽  
Locally Excited ◽  
Donor Acceptor ◽  
State Mixing

Efficient triplet-to-singlet conversion in conventional donor-acceptor TADF compounds relies on charge-transfer (CT) and locally-excited (LE) triplet state mixing as this provides required spin-orbit coupling. In this work, asymmetric carbazole-donor motif...

scholarly journals Chemical Control of Spin‐Orbit Coupling and Charge Transfer in Vacancy‐Ordered Ru(IV) Halide Perovskites

2020 ◽  
Author(s):  
Pratap Vishnoi ◽  
Julia L. Zuo ◽  
Joya A. Cooley ◽  
Linus Kautzsch ◽  
Alejandra Gómez‐Torres ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Chemical Control ◽  
Orbit Coupling ◽  
Spin Orbit Coupling ◽  
Spin Orbit ◽  
Halide Perovskites

scholarly journals Applications of model systems to explore exchange-correlation effects in density-functional theory

2020 ◽  
Author(s):  
◽  
Edward A. III Pluhar
Keyword(s):  
Charge Transfer ◽  
Magnetic Fields ◽  
Density Functional ◽  
Model System ◽  
Orbit Coupling ◽  
Model Systems ◽  
Spin Orbit Coupling ◽  
Spin Orbit ◽  
Electron Dynamics ◽  
Functional Theory

Density-functional theory (DFT), in its various forms, has become a near ubiquitous form of theoretical research used to benchmark and prototype solutions to many finite and extended state system. This is largely because DFT can both capture the rich physics that is present in these electronic systems, while remaining computationally cost-effective and interpretable. However, DFT also has the requirement that the density functional being used to iteratively converge towards a solution must be accurate and correct. While on the surface such a stipulation seems benign, in practice the density functionals can be overwhelmingly complex and error can be introduced that comes from either the density functional that is chosen or the approximations used to make a system more calculationally tenable. In this work, our focus is on the use of model systems to calculate and determine the usefulness and shortcomings of DFT. By simplifying the underlying system, while also retaining enough physical quantities from real systems, we can focus on how the approximations affect the outcomes that are produced. To begin, we show that charge-transfer dynamics can be described in unique and enlightening ways through the use of the particle-hole map (PHM). Using a one-dimensional, multi-well system, we effectively demonstrate how interesting electron dynamics can be uncovered by applying unitary transformations to the wavefunctions. By spatially localizing the electronic wavefunctions through the Foster-Boys method, which is analogous to Wannier localization in extended systems, the intermediating components of charge transfer systems can be examined to determine their effect on the system-at-large. From the simple one-dimensional system, we could quickly infer real molecular systems that could potentially be examined using the same method to surmise the role charge-transfer intermediaries play in such systems as organic photovoltaics. Beyond electron dynamics, the role of exchange-correlation (xc) scalar potentials and magnetic fields that are features of noncollinear spin Kohn-Sham (KS) and DFT was explored by comparing the exact Schroedinger solution to the KS and DFT approximations. By extending the Hubbard model to four sites, we can both solve the system exactly, while allowing for on-site and nearest-neighbor interactions. We were able to obtain benchmark solutions across a wide range of interaction strengths, determining that there are regimes where the xc magnetic fields play an increasingly larger role as the system becomes more correlated. In fact, there is a regime where the xc magnetic fields become larger than the external magnetic fields that are applied on the system. Through the model system, we could additionally compare the exact solutions against the approximated xc functionals and demonstrate that the weakly correlated regime can be adequately described by the xc functional approximations common to many real-systems. Moving beyond steady state observations, we can also describe time-dependent electron dynamics through real-time TDDFT and use a model system to compare the time-evolution of the exact and KS solutions. By allowing the xc potentials to propagate in real time, we could explore the role the xc torques played during the evolution of a triangular lattice under an applied, time-varying magnetic field. Additionally, by controlling the spin-orbit coupling present in the small model system, we determined that the spin orbit coupling plays a substantial role in keeping the spins more closely aligned with the exact system. In part, this was due to the spin-orbit coupling serving as a time-varying magnetic field, which tended to be larger than the xc potentials that were also present. The trimer can also be quickly and easily expanded with the added spin-orbit coupling and compared to real model systems through computational physics software, such as Octopus.

Theoretical investigations of electron paramagnetic resonancegfactors in ZnSe:Ti2+, CdTe:Ti2+and ZnSe:V3+crystals

2012 ◽  
Vol 45 (5) ◽  
pp. 972-975
Author(s):  
Lianxuan Zhu ◽  
Minjie Wang
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Charge Transfer ◽  
Coupling Effect ◽  
Orbit Coupling ◽  
Spin Orbit Coupling ◽  
Spin Orbit ◽  
Paramagnetic Resonance ◽  
Theoretical Investigations ◽  
The One ◽  
Electron Paramagnetic

The electron paramagnetic resonance (EPR)g-factor formulas are constructed for ZnSe:Ti2+, CdTe:Ti2+and ZnSe:V3+crystals based on the contributions of the charge-transfer levels and the spin-orbit coupling effect of the central ion and the ligands. The EPRgfactors are calculated from these formulas, and the calculated values agree well with the experimental ones. The contribution rates of the charge-transfer levels are 10.1, 7.6 and 24.9% for ZnSe:Ti2+, CdTe:Ti2+and ZnSe:V3+crystals, respectively. Thegfactors obtained from the one-spin-orbit-parameter model are also given for comparison.

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