High-Efficiency Photoinduced Charge Separation in Fe(III)carbene Thin Films

Minli Zhang; Catherine E Johnson; Aleksandra Ilic; Jesper Schwarz; Malin B Johansson; Reiner Lomoth

doi:10.1021/jacs.3c05404

High-Efficiency Photoinduced Charge Separation in Fe(III)carbene Thin Films

J Am Chem Soc. 2023 Sep 6;145(35):19171-19176. doi: 10.1021/jacs.3c05404. Epub 2023 Aug 24.

Authors

Minli Zhang¹, Catherine E Johnson¹, Aleksandra Ilic², Jesper Schwarz², Malin B Johansson¹, Reiner Lomoth¹

Affiliations

¹ Department of Chemistry - Ångström Laboratory, Uppsala University, Box 523, SE-75120 Uppsala, Sweden.
² Center for Analysis and Synthesis, Department of Chemistry, Lund University, Box 124, SE-22100 Lund, Sweden.

Abstract

Symmetry-breaking charge separation in molecular materials has attracted increasing attention for optoelectronics based on single-material active layers. To this end, Fe(III) complexes with particularly electron-donating N-heterocyclic carbene ligands offer interesting properties with a ²LMCT excited state capable of oxidizing or reducing the complex in its ground state. In this Communication, we show that the corresponding symmetry-breaking charge separation occurs in amorphous films of pristine [Fe(III)L₂]PF₆ (L = [phenyl(tris(3-methylimidazol-2-ylidene))borate]^-). Excitation of the solid material with visible light leads to ultrafast electron transfer quenching of the ²LMCT excited state, generating Fe(II) and Fe(IV) products with high efficiency. Sub-picosecond charge separation followed by recombination in about 1 ns could be monitored by transient absorption spectroscopy. Photoconductivity measurements of films deposited on microelectrode arrays demonstrated that photogenerated charge carriers can be collected at external contacts.