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Organometallic halide perovskites (OMHPs) have recently emerged as a promising class of materials in photovoltaic technology. Here, we present an in-depth investigation of the physics in these systems by measuring the photoinduced absorption (PIA) in OMHPs as a function of materials composition, excitation wavelength, and modulation frequency. We report a photoinduced Stark effect that depends on the excitation wavelength and on the dipole strength of the monovalent cations in the A position of the ABX perovskite. The results presented are corroborated by density functional theory calculations and provide fundamental information about the photoinduced local electric field change under blue and red excitation as well as insights into the mechanism of light-induced ion displacement in OMHPs. For optimized perovskite solar cell devices beyond 19% efficiency, we show that excess thermalization energy of blue photons plays a role in overcoming the activation energy for ion diffusion.
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http://dx.doi.org/10.1021/acsnano.6b07916 | DOI Listing |
ACS Appl Mater Interfaces
June 2025
Key Laboratory of Bio-Inspired Smart Interfacial Science and Technology of Ministry of Education, School of Chemistry, Beihang University, Beijing 100191, China.
Induced vacancy defects have been strategically employed to enhance the performance of semiconductor substrates for surface-enhanced Raman scattering (SERS) applications such as chemical sensing and biosensing. However, maintaining these induced vacancy defects over prolonged use remains a significant challenge, as they tend to rapidly self-heal when exposed to air. In this study, we demonstrate that chemically induced oxygen vacancy (CIVO) defects can stabilize defect sites in the metal-organic framework (MOF) SERS substrate.
View Article and Find Full Text PDFJ Phys Chem B
November 2024
Institut für Chemie, Sekr. PC14, Technische Universität Berlin, Straße des 17. Juni 135, Berlin D-10623, Germany.
A profound understanding of protein structure and mechanism requires dedicated experimental and theoretical tools to elucidate electrostatic and hydrogen bonding interactions in proteins. In this work, we employed an approach to disentangle noncovalent and hydrogen-bonding electric field changes during the reaction cascade of a multidomain protein, i.e.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
June 2024
Max Born Institut für Nichtlineare Optik und Kurzzeitspektroskopie, 12489 Berlin, Germany.
The photoinduced all-trans to 13-cis isomerization of the retinal Schiff base represents the ultrafast first step in the reaction cycle of bacteriorhodopsin (BR). Extensive experimental and theoretical work has addressed excited-state dynamics and isomerization via a conical intersection with the ground state. In conflicting molecular pictures, the excited state potential energy surface has been modeled as a pure S[Formula: see text] state that intersects with the ground state, or in a 3-state picture involving the S[Formula: see text] and S[Formula: see text] states.
View Article and Find Full Text PDFJ Am Chem Soc
May 2024
State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Fudan University, Shanghai 200438, China.
The desirable superimposed stacking of two-dimensional covalent organic frameworks (2D COFs) benefits out-of-plane charge transfer, whereas the actual stacking deviation cannot leverage the potential of 2D COFs for optoelectrical applications. Herein, we report a chirality-induced strategy to control the parallel AA-stacking sequence for the β-ketoenamine-linked COF film supported on a FTO substrate. The resulting chiral modules are periodically distributed at the framework node, ensuring identical mirrored configurations of layers for parallel stacking.
View Article and Find Full Text PDFNano Lett
March 2024
Laboratoire de physique de l'ENS, Université PSL, CNRS, Sorbonne Université, Université Paris Cité, 75005 Paris, France.
We report on the photoluminescence of pairs of organic color centers in single-wall carbon nanotubes grafted with 3,5-dichlorobenzene. Using various techniques such as intensity correlations, superlocalization microscopy, and luminescence excitation spectroscopy, we distinguish two pairs of color centers grafted on the same nanotube; the distance between the pairs is on the order of several hundreds of nanometers. In contrast, by studying the strong temporal correlations in the spectral diffusion in the framework of the photoinduced Stark effect, we can estimate the distance within each pair to be on the order of a few nanometers.
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