Spin Crossover in a Cobalt Complex on Ag(111).
Sven JohannsenSascha OssingerJan GrunwaldAlexander HermanHeiko WendeFelix TuczekManuel GruberRichard BerndtPublished in: Angewandte Chemie (International ed. in English) (2022)
The Co-based complex [Co(H 2 B(pz)(pypz)) 2 ] (py=pyridine, pz=pyrazole) deposited on Ag(111) was investigated with scanning tunneling microscopy at ≈5 K. Due to a bis(tridentate) coordination sphere the molecules aggregate mainly into tetramers. Individual complexes in these tetramers undergo reversible transitions between two states with characteristic image contrasts when current is passed through them or one of their neighbors. Two molecules exhibit this bistability while the other two molecules are stable. The transition rates vary linearly with the tunneling current and exhibit an intriguing dependence on the bias voltage and its polarity. We interpret the states as being due to S= 1 / 2 and 3 / 2 spin states of the Co 2+ complex. The image contrast and the orders-of-magnitude variations of the switching yields can be tentatively understood from the calculated orbital structures of the two spin states, thus providing first insights into the mechanism of electron-induced excited spin-state trapping (ELIESST).
Keyphrases
- single molecule
- room temperature
- density functional theory
- high resolution
- deep learning
- transition metal
- quantum dots
- ionic liquid
- atomic force microscopy
- magnetic resonance
- molecular dynamics
- open label
- randomized controlled trial
- computed tomography
- high throughput
- mass spectrometry
- study protocol
- reduced graphene oxide