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Phys. Rev. B 77, 245319 (2008) [16 pages]

Theory of resonant radiation force exerted on nanostructures by optical excitation of their quantum states: From microscopic to macroscopic descriptions

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Takuya Iida1,2,* and Hajime Ishihara1
1Department of Physics and Electronics, Osaka Prefecture University, 1-1, Gakuen-cho, Nakaku, Sakai, Osaka 599-8531, Japan
2PRESTO, Japan Science and Technology Agency, 4-1-8 Honcho Kawaguchi, Saitama 332-0012, Japan

Received 22 March 2008; revised 20 May 2008; published 19 June 2008

See accompanying Physics Focus

We establish a theoretical framework that provides a bridge between the microscopic to macroscopic descriptions of the radiation force (RF) under a quantum resonance condition. By using this framework, we derive an explicit analytical expression to clearly demonstrate the properties of the resonant RF on nanostructures and related novel phenomena. (i) For a single nano-object the RF drastically changes with the size, shape, and quality of a nano-object due to the spatial correlations of the internal radiation field and the matter-excited states. This property is highly advantageous in the selective manipulation of quantum properties of nano-objects. (ii) For multiple nano-objects an attractive (repulsive) interobject radiation force (IRF) arises between nano-objects under the optical excitation of a particular coupled state of their spatially separated polaritons, and we term this state as “polaritonic molecule.” This IRF can be enhanced even between the nano-objects that have a large spatial separation if there exist intermediate nano-objects even with very weak induced polarizations, and this effect is termed as “superinterobject radiation force.” In addition, we clarify that a “negative dissipative force” arises when the electronic polarization in a particular nano-object is inverted by a photomediated interaction. Since the resonant RF and IRF depend on many degrees of freedom of both nanostructures and light, they will provide a great variety of optical control methods for the collective dynamics of nanocomposite materials.

© 2008 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevB.77.245319
DOI:
10.1103/PhysRevB.77.245319
PACS:
78.67.Bf, 71.35.−y, 42.50.Wk, 87.80.Cc

*takuya-iida@pe.osakafu-u.ac.jp