Electronic Structure at the Perovskite/Rubrene Interface: The Effect of Surface Termination

Perovskite films have rapidly emerged as leading active materials in optoelectronic devices due to their strong optical absorption, high carrier mobility, and ease of fabrication. While proving to be promising materials for solar cells and light-emitting diodes, another application of perovskites, which makes effective use of their unique properties, is sensitization for photon upconversion. Consisting of a bulk perovskite sensitizer alongside an adjacent organic semiconductor film, the upconverting system can absorb multiple low-energy photons to emit high-energy photons. In this work, density functional theory, in conjunction with GW theory, is utilized to investigate the electronic structure at the MAPbI3/rubrene interface for different surface terminations of MAPbI3. From this investigation, we reveal that the surface termination of the perovskite layer greatly affects the charge density at the interface and within the rubrene layer, driven by the formation of interfacial dipole layers. The formation of a strong interfacial dipole for the lead-iodide-terminated perovskite alters the band alignment of the heterojunction and is expected to facilitate more efficient hole transfer, which should enhance triplet generation in rubrene through sequential charge transfer from the perovskite layer. The formation of this dipole layer is explained by the slight ionization of rubrene molecules due to the passivation of surface states and orbital hybridization. For the perovskite surface terminated with the methylammonium iodide layer, the highest occupied molecular orbital of the adjacent rubrene layer lies deep within the perovskite band gap. This termination type is further characterized by a lower density of states near the band edges and lower electron density, thereby acting as a spacer, which is anticipated to decrease the probability of charge transfer across the interface. Thus, based on our results, PbI2-terminated perovskite surfaces are predicted to be favorable for applications where hole transfer to a rubrene layer is ideal, highlighting the significance of surface termination not only for upconverting systems but for all systems where the electronic environment at the interface is crucial to performance.

Authors

Institutions

Publication Details

Journal
The Journal of Physical Chemistry C
Published
2024-12-16
DOI
https://doi.org/10.1021/acs.jpcc.4c07074
Citations
6
Primary Topic
Electronic and Structural Properties of Oxides
Type
article
Field-Weighted Citation Impact
0.70

Funders

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

Electronic Structure at the Perovskite/Rubrene Interface: The Effect of Surface Termination

Timothy W. Schmidt, Dane R. McCamey, Jared H. Cole, Christopher G. Bailey et al.
6 citations
The Journal of Physical Chemistry C
Electronic and Structural Properties of Oxides
0.70
article

Electronic Structure at the Perovskite/Rubrene Interface: The Effect of Surface Termination

Timothy W. Schmidt, Dane R. McCamey, Jared H. Cole, Christopher G. Bailey, Mykhailo V. Klymenko, Nicholas P. Sloane
article en
6 citations

Abstract

Perovskite films have rapidly emerged as leading active materials in optoelectronic devices due to their strong optical absorption, high carrier mobility, and ease of fabrication. While proving to be promising materials for solar cells and light-emitting diodes, another application of perovskites, which makes effective use of their unique properties, is sensitization for photon upconversion. Consisting of a bulk perovskite sensitizer alongside an adjacent organic semiconductor film, the upconverting system can absorb multiple low-energy photons to emit high-energy photons. In this work, density functional theory, in conjunction with GW theory, is utilized to investigate the electronic structure at the MAPbI3/rubrene interface for different surface terminations of MAPbI3. From this investigation, we reveal that the surface termination of the perovskite layer greatly affects the charge density at the interface and within the rubrene layer, driven by the formation of interfacial dipole layers. The formation of a strong interfacial dipole for the lead-iodide-terminated perovskite alters the band alignment of the heterojunction and is expected to facilitate more efficient hole transfer, which should enhance triplet generation in rubrene through sequential charge transfer from the perovskite layer. The formation of this dipole layer is explained by the slight ionization of rubrene molecules due to the passivation of surface states and orbital hybridization. For the perovskite surface terminated with the methylammonium iodide layer, the highest occupied molecular orbital of the adjacent rubrene layer lies deep within the perovskite band gap. This termination type is further characterized by a lower density of states near the band edges and lower electron density, thereby acting as a spacer, which is anticipated to decrease the probability of charge transfer across the interface. Thus, based on our results, PbI2-terminated perovskite surfaces are predicted to be favorable for applications where hole transfer to a rubrene layer is ideal, highlighting the significance of surface termination not only for upconverting systems but for all systems where the electronic environment at the interface is crucial to performance.

The Journal of Physical Chemistry CVol. 129(1)
Commonwealth Scientific and Industrial Research Organisation (AU), UNSW Sydney (AU), Data61 (AU)
Australian Government, Centre of Excellence in Exciton Science
Openalex Percentile: Top 29%
Electronic and Structural Properties of Oxides
0.70
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.