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Abstract Manipulation of nanoparticles by light induced forces is widely used in nanotechnology and bioengineering. In normal cases, when a nanoparticle is illuminated by light waves, the transfer of momentum from light to the nanoparticle can push it to move along the light propagation direction. On the other hand, the lateral optical force can transport an object perpendicular to the light propagation direction, and the optical pulling force can attract an object toward the light source. Although these optical forces have drawn growing attention, in situ tuning of them is rarely explored. In this paper, tuning of both lateral optical forces and optical pulling forces is numerically demonstrated via a graphene/α‐phase molybdenum trioxide (α‐MoO3) bilayer structure. Under plane‐wave illumination, both the amplitude and direction of the optical forces exerted on a nanoparticle above this bilayer structure can be tuned in the mid‐infrared range. The underlying mechanism can be understood by studying the corresponding isofrequency contours of the hybrid plasmon‐phonon polaritons supported by the graphene/α‐MoO3bilayer. The analytical study using the dipole approximation method reproduces the numerical results, revealing the origin of the optical forces. This work opens a new avenue for engineering optical forces to manipulate various objects optically.
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Nonequilibrum phase transition in the light-actuated self-assembly of nanoparticles: effects of surfaces and stochastic forces
When we illuminate gold nanofluids over indium-tin-oxide (ITO)-coated substrates, nanoparticle chains selfassemble via optical binding forces. We speculate that charge transfer between gold and ITO pins nanoparticles to the substrate and reduces the lateral Brownian motion as they attach to the substrate. We correspondingly model the self assembly with additional stochastic or random forces. Simulations show a nonequilibrium phase transition: when the stochastic force is small, nanoparticle chains align perpendicular to the light polarization and nanoparticles settle at shallow but stable nodes; when the stochastic force is large, however, the nanoparticle chains align parallel to the light polarization and nanoparticles settle at saddlepoints where the optical binding force is largely zero. Since the presence and strength of Brownian forces influence which state is formed, we reconsider the role that surfaces have—not only in relation to charge transfer but also heat transfer.
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- Award ID(s):
- 1921034
- PAR ID:
- 10166399
- Date Published:
- Journal Name:
- Optical Trapping and Optical Micromanipulation
- Volume:
- 11083
- Issue:
- XVI
- Page Range / eLocation ID:
- 1108325
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript
- Conference Paper:
- https://doi.org/10.1117/12.2528987
