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Correction: Size and shape dependent photoluminescence and excited state decay rates of diamondoids
Robert
Richter
*a,
David
Wolter
a,
Tobias
Zimmermann
a,
Lasse
Landt
a,
Andre
Knecht
a,
Christoph
Heidrich
a,
Andrea
Merli
a,
Otto
Dopfer
a,
Philipp
Reiß
b,
Arno
Ehresmann
b,
Jens
Petersen
c,
Jeremy E.
Dahl
d,
Robert M. K.
Carlson
d,
Christoph
Bostedt
e,
Thomas
Möller
a,
Roland
Mitric
c and
Torbjörn
Rander
*a
aInstitut für Optik und Atomare Physik, Technische Universität Berlin, Hardenbergstr. 36, 10623 Berlin, Germany. E-mail: robert.richter@tu-berlin.de
bInstitute of Physics and Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel, Heinrich-Plett-Str. 40, 34132 Kassel, Germany
cUniversität Würzburg, Institut für Physikalische und Theoretische Chemie, Am Hubland, 97074 Würzburg, Germany
dStanford Institute for Materials and Energy Sciences, Stanford University, Stanford, California 94305, USA
eSLAC National Accelerator Laboratory, Menlo Park, California 94025, USA
First published on 24th November 2015
Abstract
Correction for ‘Size and shape dependent photoluminescence and excited state decay rates of diamondoids’ by Robert Richter et al., Phys. Chem. Chem. Phys., 2014, 16, 3070–3076.
The authors would like to make the following correction to their article:
In Fig. 5, the second emission spectrum for the bottom (dia (D3d)) is shifted to higher energies and should be as seen in Fig. 1 below.
 | ||
| Fig. 1 Measured photoluminescence spectra (red) and absorption spectra (black) of selected isomers of the five smallest members of the diamondoid series. The excitation energy used to record the PL is marked with an asterisk and Egap is marked with a blue arrow. PL-spectra of adamantine (ΔE = 100 meV), diamantane (ΔE = 100 meV), other spectra (ΔE = 25 meV, the spectra have been smoothed for presentation purposes). | ||
It has to be noted that by now, spectra with higher resolution are available. These can be found in ref. 1.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
References
- R. Richter, M. I. S. Röhr, T. Zimmermann, J. Petersen, C. Heidrich, R. Rahner, T. Möller, J. E. Dahl, R. M. K. Carlson, R. Mitric, T. Rander and A. Merli, Phys. Chem. Chem. Phys., 2015, 17, 4739 RSC.
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