Browsing by Author "Yeh, J. M."

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A facile method to prepare "green" nano-phosphors with a large Stokes-shift and solid-state enhanced photophysical properties based on surface-modified gold nanoclusters
(2017-12-15)
Cheng, C. H.
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Huang, H. Y.
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Talite, M. J.
;
Chou, W. C.
;
Yeh, J. M.
Colloidal nano-materials, such as quantum dots (QDs) have been applied to light-conversion nano phosphors due to their unique tunable emission. However, most of the QDs involve toxic elements and are synthesized in a hazardous solvent. In addition, conventional QD nano-phosphors with a small Stokes shift suffered from reabsorption losses and aggregation-induced quenching in the solid state. Here, we demonstrate a facile, matrix-free method to prepare eco-friendly nano-phosphors with a large Stokes shift based on aqueous thiolate-stabilized gold nanoclusters (GSH-AuNCs) with simple surface modifications. Our method is just to drop GSH-AuNCs solution on the aluminum foil and then surface modified AuNCs (Al-GSH-AuNCs) can be spontaneously precipitated out of the aqueous solution. Compared with pristine GSH-AuNCs in solution, the Al-GSH-AuNCs exhibit enhanced solid-state PL quantum yields, lengthened PL lifetime, and spectral blue shift, which can be attributed to the aggregation induced emission enhancement facilitated by surface modifications. Such surface-treatment induced aggregation of AuNCs can restrict the surface-ligand motion, leading to the enhancement of PL properties in the solid state. In addition, the Al-GSH-AuNCs nano-phosphors with a large Stokes shift can mitigate the aggregation-induced PL quenching and reabsorption losses, which would be potential candidates for "green" nano-phosphors. (C) 2017 Elsevier Inc. All rights reserved.
Hybrid Dendrimer/Semiconductor Nanostructures with Efficient Energy Transfer via Optical Waveguiding
(2015-03-05)
Lin, T. N.
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Huang, J. C.
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Shen, J. L.
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Chu, C. M.
;
Yeh, J. M.
In this study, we demonstrated a nonradiative energy transfer between InGaN quantum wells (QWs) and polyamidoamine (PAMAM) dendrimers through optical waveguiding by detecting a reduction in the photoluminescence lifetime. The maximum energy transfer efficiency of this system is similar to 72%, which is promising for sensor applications. The energy transfer efficiency depends on the distance between the InGaN QWs and PAMAM dendrimers by a factor of 1/d(2), revealing layer-to-layer dipole interactions. Upon increasing the generation of PAMAM dendrimers, the transfer energy efficiency increases exponentially, which can be explained by the increased surface coverage for the higher generation.