TY - GEN
T1 - From mapping to manipulation
T2 - 8th Molecular and Nanophotonic Machines, Devices, and Applications
AU - de Jong, Flip
AU - Diez-Silva, Pablo
AU - Chen, Jui Kai
AU - Seth, Sudipta
AU - Balakrishnan, Harishankar
AU - Shih, Bing Yang
AU - Rosmeulen, Maarten
AU - Rocha, Susana
AU - Klymchenko, Andrey
AU - Liz-Marzán, Luis
AU - Bresolí-Obach, Roger
AU - Marqués, Manuel I.
AU - Buscalioni, Rafael Delgado
AU - Hofkens, Johan
AU - Louis, Boris
N1 - Publisher Copyright:
© 2025 SPIE. All rights reserved.
PY - 2025/9/19
Y1 - 2025/9/19
N2 - The precise manipulation of nanoscale particles is essential for advancing applications in colloidal self-assembly, targeted sorting, and emerging paradigms such as colloidal memory. Here, we present a high-speed multiplane 3D imaging platform that enables direct visualization and quantification of dielectrophoretic (DEP) forces and electrokinetic flows acting on individual nanoparticles in real time. Using 200 nm dye-doped polystyrene particles, we map both positive and negative DEP regimes, capturing spatial force distributions with sub-50 nm axial resolution and frame rates exceeding 100 fps. Our approach reveals distinct particle behaviors across frequency regimes, including trapping near electrodes under positive DEP and levitation above the surface under negative DEP. In addition, we characterize electrokinetic flow fields in 3D, which play a critical role at higher voltages. This methodology provides a robust experimental framework for investigating DEP manipulation schemes, validating theoretical models, and selectively addressing particle mixtures, a key requirement for future molecular machines and frequency-controlled colloidal memory systems.
AB - The precise manipulation of nanoscale particles is essential for advancing applications in colloidal self-assembly, targeted sorting, and emerging paradigms such as colloidal memory. Here, we present a high-speed multiplane 3D imaging platform that enables direct visualization and quantification of dielectrophoretic (DEP) forces and electrokinetic flows acting on individual nanoparticles in real time. Using 200 nm dye-doped polystyrene particles, we map both positive and negative DEP regimes, capturing spatial force distributions with sub-50 nm axial resolution and frame rates exceeding 100 fps. Our approach reveals distinct particle behaviors across frequency regimes, including trapping near electrodes under positive DEP and levitation above the surface under negative DEP. In addition, we characterize electrokinetic flow fields in 3D, which play a critical role at higher voltages. This methodology provides a robust experimental framework for investigating DEP manipulation schemes, validating theoretical models, and selectively addressing particle mixtures, a key requirement for future molecular machines and frequency-controlled colloidal memory systems.
UR - https://www.scopus.com/pages/publications/105023082331
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:001729292300007&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.1117/12.3063818
DO - 10.1117/12.3063818
M3 - Conference contribution
AN - SCOPUS:105023082331
T3 - Proceedings of SPIE - The International Society for Optical Engineering
BT - Molecular and Nanophotonic Machines, Devices, and Applications VIII
A2 - Sekkat, Zouheir
A2 - Omatsu, Takashige
PB - SPIE
Y2 - 3 August 2025 through 5 August 2025
ER -