The ensemble averaged spin dephasing rate of localized electrons in the organic molecule tris(8-hydroxyquinoline aluminum) or Alq3 has been found to be significantly larger in bulk powder than in single- or few-molecule clusters confined within 1–2 nm sized nanocavities [B. Kanchibotla et al., Phys. Rev. B78, 193306 (2008)]. To understand this observation, we have compared the midinfrared absorption spectra of bulk powder and single- or few-molecule clusters. It appears that molecules have additional vibrational modes in bulk powder possibly due to multimerization. Their coupling with spin may be responsible for the increased spin dephasing rate in bulk powder
Understanding the decoherence of electron spins in semiconductors due to their interaction with nucl...
Spin–lattice relaxation is a key open problem to understand the spin dynamics of single-molecule mag...
Nanoporous materials are excellent candidates for the fabrication of molecular rotors in the solid s...
Recently, it was found that the strongly temperature-dependent spin dephasing time of bound electron...
We report a measurement of the ensemble-averaged transverse spin relaxation time (T∗2) in bulk and f...
Very recently the closely related fields of molecular spin qubits, single ion magnets and single ato...
This paper presents a detailed study of the effect of spin‐quantization and spin–orbit coupling on t...
A self-assembled cylindrical capsule provides a nanoscale environment that affects the rotational ba...
A self-assembled cylindrical capsule provides a nanoscale environment that affects the rotational ba...
Single molecule magnets (SMMs), such as Mn12-acetate, are composed of transition metal ions and cons...
We report slow correlated growth mode in energetic cluster vapor deposited organic light emissive ma...
We study the quantum spin dynamics of nearly isotropic Gd3+ ions entrapped in polyoxometalate molecu...
Optical dephasing of pentacene dimers in p-terphenyl is studied. Dimer states R3 and R4 exhibit an e...
Molecular magnets are ideal systems to probe the realm that borders quantum and classical physics, a...
Bad vibrations? $^{161}$Dy nuclear resonance vibrational spectroscopy gives direct experimental acce...
Understanding the decoherence of electron spins in semiconductors due to their interaction with nucl...
Spin–lattice relaxation is a key open problem to understand the spin dynamics of single-molecule mag...
Nanoporous materials are excellent candidates for the fabrication of molecular rotors in the solid s...
Recently, it was found that the strongly temperature-dependent spin dephasing time of bound electron...
We report a measurement of the ensemble-averaged transverse spin relaxation time (T∗2) in bulk and f...
Very recently the closely related fields of molecular spin qubits, single ion magnets and single ato...
This paper presents a detailed study of the effect of spin‐quantization and spin–orbit coupling on t...
A self-assembled cylindrical capsule provides a nanoscale environment that affects the rotational ba...
A self-assembled cylindrical capsule provides a nanoscale environment that affects the rotational ba...
Single molecule magnets (SMMs), such as Mn12-acetate, are composed of transition metal ions and cons...
We report slow correlated growth mode in energetic cluster vapor deposited organic light emissive ma...
We study the quantum spin dynamics of nearly isotropic Gd3+ ions entrapped in polyoxometalate molecu...
Optical dephasing of pentacene dimers in p-terphenyl is studied. Dimer states R3 and R4 exhibit an e...
Molecular magnets are ideal systems to probe the realm that borders quantum and classical physics, a...
Bad vibrations? $^{161}$Dy nuclear resonance vibrational spectroscopy gives direct experimental acce...
Understanding the decoherence of electron spins in semiconductors due to their interaction with nucl...
Spin–lattice relaxation is a key open problem to understand the spin dynamics of single-molecule mag...
Nanoporous materials are excellent candidates for the fabrication of molecular rotors in the solid s...