1
Supporting Information
The Nature of Non-FRET Photoluminescence Quenching in
Nanoassemblies from Semiconductor Quantum Dots and Dye Molecules
Aleksander P. Stupak
a
, Thomas Blaudeck
b#
, Eduard I. Zenkevich
c
, Stefan
Krause
b,&
, and Christian von Borczyskowski
b*
a
B. I. Stepanov Institute of Physics, National Academy of Sciences of Belarus,
Prospect Nezavisimosti 70, 220072 Minsk, Belarus
b
Institute of Physics and Center for Nanostructured Materials and Analytics, Technische Universität
Chemnitz, Reichenhainer Str. 70, D-09107 Chemnitz, Germany
c
Department of Information Technologies and Robotics, National Technical University of Belarus,
Prospect Nezavisimosti 65, 220013 Minsk, Belarus
#
Present address: Department of Electrical Engineering and Information Technology, Center for
Microtechnologies, Technische Universität Chemnitz, Reichenhainer Str. 70, D-09107 Chemnitz,
Germany
&
Present address: Department of Chemistry, University of Copenhagen, Universitätsparken 5, 2100
Copenhagen, Denmark
*
Corresponding Author: C. von Borczyskowski: borczyskowski@physik.tu-chemnitz.de
S1 Analysis of QD PL Intensity Quenching
For the analysis of the PL intensity quenching as a function of the number of porphyrin
molecules per QD, the well-known Stern-Volmer formalism [1] was modified. In our more
generalized approach, the luminescence quenching can be described by
. (S1) dx x K
x I
I
) ( 1
) (
0
0
(x) and represent the integrated PL intensity of the QD in presence ( (x)) and absence I I
0
I
( ) of the chromophores, respectively. In this approach, the Stern-Volmer function I
0
) ( x K
depends explicitly on the ratio x of (m-Pyr)
4
H
2
P to QD molar concentrations and can be
expressed by the first derivative K
SV
D
(x of the experimental data plotted in conventional
Stern-Volmer representation [2, 3]. “D” stands for the QD as a possible donor in FRET
related processes. Using this approach, the corresponding K
SV
A
values have been derived from
the acceptor A (H
2
P) fluorescence enhancement measurements at every titration step.
References
[1] B. Valeur. Wiley-VCH (2002) Weinheim.
Electronic Supplementary Material (ESI) for Physical Chemistry Chemical Physics.
This journal is © the Owner Societies 2018