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  • Structural insights to metal ion linked multilayers on metal oxide surfaces via energy transfer and polarized ATR measurements
Title: Structural insights to metal ion linked multilayers on metal oxide surfaces via energy transfer and polarized ATR measurements
Metal ion linked multilayers offer a means of controlling interfacial energy and electron transfer for a range of applications including solar energy conversion, catalysis, sensing, and more. Despite the importance of structure to these interlayer transfer processes, little is known about the distance and orientation between the molecules/surface of these multilayer films. Here we gain structural insights into these assemblies using a combination of UV-Vis polarized visible attenuated total reflectance (p-ATR) and Förster Resonance Energy Transfer (FRET) measurements. The bilayer of interest is composed of a metal oxide surface, phosphonated anthracene molecule, Zn(II) linking ion, and a platinum porphyrin with one (P1), two (P2), or three (P3) phenylene spacers between the chromophoric core and the metal ion binding carboxylate group. As observed by both time-resolved emission and transient absorption, the FRET rate and efficiency decreases with an increasing number of phenylene spacers (P1 > P2 > P3). However, from p-ATR measurements we observe a change in orientation of porphyrins in the bilayer, which inhibits a uniform determination of the orientation factor (κ2) across the series. Instead, we narrow the scope of viable structures by determining the best agreement between experimental and calculated FRET efficiencies. Additionally, we provide evidence that suggests, for the first time, that the bilayer structure is similar on both planar and mesoporous substrates.  more » « less
Award ID(s):
2327754
PAR ID:
10572085
Author(s) / Creator(s):
; ; ; ; ; ; ; ; ; ;
Publisher / Repository:
Royal Chemical Society
Date Published:
Journal Name:
Journal of Materials Chemistry A
Volume:
12
Issue:
42
ISSN:
2050-7488
Page Range / eLocation ID:
28882 to 28891
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
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