Mack E, Cadranel A, Guldi DM, Harrer E, Zhou X, Wu M, Lourenço LM, Zahn D, Spiecker E, Backes C, Guldi DM (2025)
Publication Language: English
Publication Type: Journal article
Publication year: 2025
Book Volume: 19
Pages Range: 28576-28587
Journal Issue: 31
Interfacial charge-transfer (ICT) hybrids including transition metal dichalcogenides (TMDs) and phthalocyanines were synthesized and thoroughly characterized. The amount of noncovalently immobilized phthalocyanines per liquid-phase exfoliated (LPE) TMD flake increased exponentially with decreasing flake thickness. Steady-state spectroscopy revealed strong ground-state electronic coupling, evidenced by the emergence of distinct ICT bands. This allowed us to quantify ICT interactions in TMDs using a Mulliken-Hush approach. Also, strong excited-state electronic coupling led to significant quenching of phthalocyanine-centered fluorescence. Ultrafast transient absorption spectroscopy confirmed the formation of charge-separated states with lifetimes on the order of hundreds of picoseconds. These lifetimes remained largely unaffected by the number of TMD layers, underscoring the predominant role of surface-centered ICT interactions. Interestingly, depending on the relative alignment of electronic energy levels at the phthalocyanine/TMD interface, bidirectional charge transfer was also observed.
APA:
Mack, E., Cadranel, A., Guldi, D.M., Harrer, E., Zhou, X., Wu, M.,... Guldi, D.M. (2025). Morphological and Electronic Control of Interfacial Charge Transfer in 2D Transition Metal Dichalcogenide Hybrids. ACS nano, 19(31), 28576-28587. https://doi.org/10.1021/acsnano.5c07850
MLA:
Mack, Elena, et al. "Morphological and Electronic Control of Interfacial Charge Transfer in 2D Transition Metal Dichalcogenide Hybrids." ACS nano 19.31 (2025): 28576-28587.
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