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Spin Crossover in a Cobalt Complex on Ag(111)

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 rever...

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Detalles Bibliográficos
Autores principales: Johannsen, Sven, Ossinger, Sascha, Grunwald, Jan, Herman, Alexander, Wende, Heiko, Tuczek, Felix, Gruber, Manuel, Berndt, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303790/
https://www.ncbi.nlm.nih.gov/pubmed/35032345
http://dx.doi.org/10.1002/anie.202115892
Descripción
Sumario: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).