Please use this identifier to cite or link to this item:
|Title:||Enhanced luminescence and charge separation in polythiophene-grafted, gold nanoparticle-decorated, 1-D ZnO nanorods|
|Citation:||Jayaraman, S., Kumar, P.S., Mangalaraj, D., Rajarathnam, D., Ramakrishna, S., Srinivasan, M.P. (2014). Enhanced luminescence and charge separation in polythiophene-grafted, gold nanoparticle-decorated, 1-D ZnO nanorods. RSC Advances 4 (22) : 11288-11294. ScholarBank@NUS Repository. https://doi.org/10.1039/c3ra45953e|
|Abstract:||In this work, we demonstrate a facile method for fabricating hybrid organic/inorganic structures of vertically oriented 1-dimensional (1-D) ZnO nanorods (NR) coupled with regio-regular poly(3-(2-methoxyethoxy) ethoxymethyl) thiophene-2,5-diyl (PMEEMT). The NRs were synthesized by two-step solution processes and exhibited a hexagonal wurtzite structure with a lattice spacing of 0.248 nm. Cross-section analysis of field-emission scanning electron microscopy (FESEM) analysis confirmed the NRs were vertically oriented and densely packed with diameter of about 250 nm. The hybrid structures were formed by encapsulating the ZnO NRs with polythiophenes, thereby creating a direct heterojunction interface. These interfaces allowed easy electron transport along the NR avoiding loss of mobility due to grain boundary scattering; further, the large aspect ratio and surface area of NR increased the effective interface between polythiophene and the nanorods contributing to efficient charge separation. In addition, decoration of the ZnO hybrid structures by gold nanoparticles (AuNPs) induced enhanced luminescence properties. These functionalized organic/inorganic hybrid structures can pave the way for applications in photovoltaics and sensing. © 2014 The Royal Society of Chemistry.|
|Source Title:||RSC Advances|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Aug 14, 2018
WEB OF SCIENCETM
checked on Aug 7, 2018
checked on Aug 10, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.