arXiv subjects

Gauthami Viswan

Publications and source records attributed to Gauthami Viswan.

3 recordsLinked to original sources

arXiv2026

Switchable circular dichroism and ionic migration dominated charge transport in a chiral spin crossover polymer

We demonstrate thermally switchable chiroptical activity in a chiral spin crossover (SCO) material, where circular dichroism is significant in the low spin state but quenched in the high-spin state for both enantiomers. With magnetometry we establish a cooperative transition with hysteresis near room temperature. Fe L3,2 edge Xray absorption directly links the quenching of chirality to a reorganization of Fe 3d electronic structure that accompanies the spin state transition. Moreover, electrical measurements show pronounced I(V) hysteresis and cycling dependent C(V) behavior, indicating transport in this chiral SCO material is dominated by ionic migration rather than mobile electrons or holes.

cond-mat.mtrl-sci↗

arXiv2024

Chiral effects at the metal center in Fe(III) spin crossover coordination salts

Evidence of chirality was observed at the Fe metal center in Fe(III) spin crossover coordination salts [Fe(qsal)2][ Ni(dmit)2] and [Fe(qsal)2](TCNQ)2 from X-ray absorption spectroscopy at the Fe 2p3/2 core threshold. This indicates the formation of chiral domains that influence the octahedral coordination on the Fe core.

cond-mat.mtrl-sci↗

arXiv2024

The surface termination of a Fe (III) spin crossover molecular salt

From a comparison of energy dispersive analyses of X-rays (EDAX), the known molecular stoichiometry and X-ray photoemission spectroscopy (XPS), it is evident that the Fe(III) spin crossover salt [Fe(qsal)2Ni(dmit)2] has a preferential surface termination with the Ni(dmit)2 moiety. This preferential surface termination leads to a significant surface to bulk core level shift for the Ni 2p X-ray photoemission core level, not seen in the corresponding Fe 2p core level spectra. Inverse photoemission spectroscopy (IPES), thus provides some indication of the density of states resulting from the dmit2 = 1,3-dithiol-2-thione-4,5-dithiolato ligand unoccupied molecular orbitals.

cond-mat.mtrl-sci↗