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Nanosecond Time‐Resolution Study of Gold Nanorod Rotation at the Liquid–Solid Interface
Author(s) -
Neupane Bhanu,
Chen Fang,
Wei Yanli,
Fang Ning,
Ligler Frances S.,
Wang Gufeng
Publication year - 2016
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201600174
Subject(s) - nanorod , nanosecond , rotation (mathematics) , particle (ecology) , chemical physics , nanotechnology , adsorption , materials science , particle size , nanoparticle , rotation around a fixed axis , chemistry , chemical engineering , molecular physics , optics , physics , classical mechanics , laser , oceanography , geometry , mathematics , geology , engineering
Early studies showed that the adsorption of nanorods may start from a special “anchored” state, in which the nanorods lose translational motion but retain rotational freedom. Insight into how the anchored nanorods rotate should provide additional dimensions for understanding particle–surface interactions. Based on conventional time‐resolution studies, gold nanorods are thought to continuously rotate following initial interactions with negatively charged glass surfaces. However, this nanosecond time‐resolution study reveals that the apparent continuous rotation actually consists of numerous fast, intermittent rotations or transitions between a small number of weakly immobilized states, with the particle resting in the immobilized states most of the time. The actual rotation from one immobilized state to the other happens on a 1 ms timescale, that is, approximately 50 times slower than in the bulk solution.