TY - JOUR
T1 - Electrostatic formation of quantum dot/J-aggregate FRET pairs in solution
AU - Halpert, Jonathan E.
AU - Tischler, Jonathan R.
AU - Nair, Gautham
AU - Walker, Brian J.
AU - Liu, Wenhao
AU - Bulović, Vladimir
AU - Bawendi, Moungi G.
PY - 2009/6/11
Y1 - 2009/6/11
N2 - We report the formation and photonic properties of CdSe/ZnS quantum dot (QD)/J-aggregate donor-acceptor Forster resonant energy transfer (FRET) pairs that are electrostatically bound and dispersed in water. Assembly occurs when the positively charged dye, 1,1',3,3'-tetraethyl-5,5',6,6'- tetrachlorobenzimidazolocarbocyanine (TTBC), binds electrostatically to QDs that are coated with a negatively charged amphiphilic polymer. QD/ J-aggregate FRET pairs display the broadband absorption in the visible and the ultraviolet (UV) part of the spectrum typical of quantum dots, along with the narrow emission linewidths characteristic of J-band emitters (∼12 nm full width at half-maximum). We use dynamic light scattering, transmission electron microscopy, photoluminescence spectroscopy, and photoluminescence lifetimes to conclude that the size of the aggregates formed in the presence of QDs is between 1-6 nm. We find the FRET radius of the QD/J-aggregate to be 5.1 nm. We further demonstrate electrostatic binding as a general synthetic strategy for these types of FRET pairs by attaching a negatively charged J-aggregate (BIC) to a quantum dot coated with positively charged ligands.
AB - We report the formation and photonic properties of CdSe/ZnS quantum dot (QD)/J-aggregate donor-acceptor Forster resonant energy transfer (FRET) pairs that are electrostatically bound and dispersed in water. Assembly occurs when the positively charged dye, 1,1',3,3'-tetraethyl-5,5',6,6'- tetrachlorobenzimidazolocarbocyanine (TTBC), binds electrostatically to QDs that are coated with a negatively charged amphiphilic polymer. QD/ J-aggregate FRET pairs display the broadband absorption in the visible and the ultraviolet (UV) part of the spectrum typical of quantum dots, along with the narrow emission linewidths characteristic of J-band emitters (∼12 nm full width at half-maximum). We use dynamic light scattering, transmission electron microscopy, photoluminescence spectroscopy, and photoluminescence lifetimes to conclude that the size of the aggregates formed in the presence of QDs is between 1-6 nm. We find the FRET radius of the QD/J-aggregate to be 5.1 nm. We further demonstrate electrostatic binding as a general synthetic strategy for these types of FRET pairs by attaching a negatively charged J-aggregate (BIC) to a quantum dot coated with positively charged ligands.
UR - http://www.scopus.com/inward/record.url?scp=67649995872&partnerID=8YFLogxK
U2 - 10.1021/jp8099169
DO - 10.1021/jp8099169
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SN - 1932-7447
VL - 113
SP - 9986
EP - 9992
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 23
ER -