Dr. Wiebke Albrecht
Ornstein Laboratory, room 18
Princetonplein 1, 3584 CC Utrecht
P.O. Box 80 000, 3508 TA Utrecht
phone: +31(0)30 253 2315
secretariat: +31(0)30 253 2952
Worked as a postdoc till June 1, 2017
Promotor: Prof.dr. A. van Blaaderen
Employed since January 2013
Funded by ERC
Transmission electron microscopy (TEM), Multiphoton confocal microscopy, UV-VIS spectroscopy, Electron energy loss spectroscopy (EELS)
Due to potential technological applications as in data storage , catalysis  or medicine  the structural deformation of uncoated gold nanorods (Au NRs) has attracted much scientific attention. However, little effort has been made to study the heat-induced deformation behavior of coated gold nanorods. Coatings of metallic nanoparticles with silica can enhance the thermal and colloidal stability of the particle and additionally influence the deformation process. Au NRs have two plasmon resonances associated with their shape. The longitudinal surface plasmon (LSP) resonance is tunable with the aspect ratio of the rod. By exciting this resonance with an ultra-short high-intense laser pulse the NR undergoes a shape transformation well below bulk melting temperatures.
The aim of this research project is to execute and analyze the deformation process of the same single particles before and after deformation as shown in figure 1a, including particles which are part of 2D or 3D self-assembled structures. Single-particle EELS measurements, shown in figure 1b, confirm the corresponding shift of the LSP peak. Furthermore, we compare the deformation process due to laser excitation and external heating. The underlying deformation mechanisms seem to be very different. The methodology will be also extended to semiconductor NRs.
Figure 1: a) Laser-induced deformation of mesoporous silica-coated Au NRs. Different deformation stages occur depending on the laser intensity. b) EELS measurements on undeformed (left) and deformed (right) particles.
 P. Zijlstra et al., Nature 459, 410-413 (2009)
 P.G.N. Mertens et al., Applied Catalysis A: General 355, 176-183 (2009)
 L. C. Kennedy et al., Small 7, 169-183 (2011)