Charge Transfer of Metal Porphyrins on a NaCl Thin Film Observed by Scanning Tunneling Microscopy in the Transport Gap

Elucidating the electronic structure of organic molecules in contact with a dielectric layer is essential to understanding and controlling many important processes, such as catalysis, photochemistry, and electroluminescence. However, this challenge calls for a detailed characterization of molecule-dielectric contacts on the atomic scale. Here, we employ scanning tunneling microscopy (STM) at low temperature (4 K) in combination with ab initio calculations to investigate the subnanometer-scale electronic states of photoactive molecules on a dielectric surface. For platinum and palladium octaethylporphyrin (PtOEP and PdOEP) adsorbed on few layers of NaCl on a metal substrate, our STM imaging of them in the energy gap between the frontier orbitals demonstrates their high sensitivity to the local environment, namely, adsorption site and applied voltage. Our calculations reveal that the states in this energy gap originate from combinations of molecular orbitals far from the Fermi level and that they are affected by the extent of molecule-surface partial charge transfer, which is tuned by adsorption site and voltage in the tunnel junction.

Authors

Institutions

Publication Details

Journal
ACS Nano
Published
2025-05-07
DOI
https://doi.org/10.1021/acsnano.5c01235
Citations
1
Primary Topic
Surface Chemistry and Catalysis
Type
article
Field-Weighted Citation Impact
0.67

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Charge Transfer of Metal Porphyrins on a NaCl Thin Film Observed by Scanning Tunneling Microscopy in the Transport Gap

Klaus Kuhnke, Fábio J. R. Costa, Klaus Kern, Kelvin Anggara et al.
1 citations
ACS Nano
Surface Chemistry and Catalysis
0.67
article

Charge Transfer of Metal Porphyrins on a NaCl Thin Film Observed by Scanning Tunneling Microscopy in the Transport Gap

Klaus Kuhnke, Fábio J. R. Costa, Klaus Kern, Kelvin Anggara, Abhishek Grewal, Christopher C. Leon, Li-Qing Zheng
article en
1 citations

Abstract

Elucidating the electronic structure of organic molecules in contact with a dielectric layer is essential to understanding and controlling many important processes, such as catalysis, photochemistry, and electroluminescence. However, this challenge calls for a detailed characterization of molecule-dielectric contacts on the atomic scale. Here, we employ scanning tunneling microscopy (STM) at low temperature (4 K) in combination with ab initio calculations to investigate the subnanometer-scale electronic states of photoactive molecules on a dielectric surface. For platinum and palladium octaethylporphyrin (PtOEP and PdOEP) adsorbed on few layers of NaCl on a metal substrate, our STM imaging of them in the energy gap between the frontier orbitals demonstrates their high sensitivity to the local environment, namely, adsorption site and applied voltage. Our calculations reveal that the states in this energy gap originate from combinations of molecular orbitals far from the Fermi level and that they are affected by the extent of molecule-surface partial charge transfer, which is tuned by adsorption site and voltage in the tunnel junction.

ACS NanoVol. 19(19)
Universidade Estadual de Campinas (UNICAMP) (BR), Max Planck Institute for Solid State Research (DE), Institut de Physique (FR), École Polytechnique Fédérale de Lausanne (CH)
Alexander von Humboldt-Stiftung, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Openalex Percentile: Top 32%
Surface Chemistry and Catalysis
0.67
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.