Characterizing Concentrated, Multiply Scattering, and Actively Driven Fluorescent Systems with Confocal Differential Dynamic Microscopy

被引:90
作者
Lu, Peter J. [1 ,2 ]
Giavazzi, Fabio [3 ]
Angelini, Thomas E. [1 ,2 ]
Zaccarelli, Emanuela [4 ,5 ]
Jargstorff, Frank [6 ]
Schofield, Andrew B. [7 ]
Wilking, James N. [1 ,2 ]
Romanowsky, Mark B. [1 ,2 ]
Weitz, David A. [1 ,2 ]
Cerbino, Roberto [3 ]
机构
[1] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
[2] Harvard Univ, SEAS, Cambridge, MA 02138 USA
[3] Univ Milan, Dipartimento Chim Biochim & Biotecnol Med, I-20090 Milan, Italy
[4] Univ Roma La Sapienza, CNR ISC, I-00185 Rome, Italy
[5] Univ Roma La Sapienza, Dipartimento Fis, I-00185 Rome, Italy
[6] NVIDIA, Santa Clara, CA 95050 USA
[7] Univ Edinburgh, Dept Phys, Edinburgh EH9 3JZ, Midlothian, Scotland
基金
美国国家科学基金会;
关键词
SUSPENSIONS; PARTICLES;
D O I
10.1103/PhysRevLett.108.218103
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
We introduce confocal differential dynamic microscopy (ConDDM), a new technique yielding information comparable to that given by light scattering but in dense, opaque, fluorescent samples of micron-sized objects that cannot be probed easily with other existing techniques. We measure the correct wave vector q-dependent structure and hydrodynamic factors of concentrated hard-sphere-like colloids. We characterize concentrated swimming bacteria, observing ballistic motion in the bulk and a new compressed-exponential scaling of dynamics, and determine the velocity distribution; by contrast, near the coverslip, dynamics scale differently, suggesting that bacterial motion near surfaces fundamentally differs from that of freely swimming organisms.
引用
收藏
页数:5
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