Study of Oscillating Electroosmotic Flows with High Temporal and Spatial Resolution Wei Zhao, , Xin Liu, Fang Yang, § Kaige Wang, Jintao Bai, Rui Qiao,* , and Guiren Wang* , Institute of Photonics and Photon-technology, International Scientic and Technological Cooperation Base of Photoelectric Technology and Functional Materials and Application, Northwest University, 229 North Taibai Road, Xian 710069, Peoples Republic of China Department of Mechanical Engineering & Biomedical Engineering Program, University of South Carolina, Columbia, South Carolina 29208, United States § Key Laboratory for Molecular Enzymology and Engineering of Ministry of Education, Jilin University, Changchun 130012, Peoples Republic of China Department of Mechanical Engineering, Virginia Tech, Blacksburg, Virginia 24061, United States * S Supporting Information ABSTRACT: Near-wall velocity of oscillating electroosmotic ow (OEOF) driven by an AC electric eld has been investigated using a laser-induced uorescence photobleaching anemometer (LIFPA). For the rst time, an up to 3 kHz velocity response of OEOF has been successfully measured experimentally, even though the oscillating velocity is as low as 600 nm/s. It is found that the oscillating velocity decays with the forcing frequency f f as f f 0.66 . In the investigated range of electric eld intensity (E A ), below 1 kHz, the linear relation between oscillating velocity and E A is also observed. Because the oscillating velocity at high frequency is very small, the contribution of noise to velocity measurement is signicant, and it is discussed in this manuscript. The investigation reveals the instantaneous response of OEOF to the temporal change of electric elds, which exists in almost all AC electrokinetic ows. Furthermore, the experimental observations are important for designing OEOF-based micro/nanouidics systems. I n micro- and nanouidic systems, due to the large surface-to- volume ratio, electroosmotic ow (EOF) has been widely used to pump uids and manipulate objects for various applications, such as DNA transport, hybridization and separation in biomedical engineering, and enhancing heat and mass transfer. 15 At the early stages, most of the investigations focused on the EOF driven by direct current (DC). The relevant devices have been proven to be eective in driving ows in micro/ nanochannels, which are further used to transport DNA, protein, and cells. However, when the length of channels is long, it normally requires high voltage to generate suciently strong electric eld to drive the ow. This leads to several drawbacks, such as gas bubble formation due to electrolysis and excessive heating due to electrothermal eects. Relative to DC EOF, the EOF generated by AC electric elds (i.e., AC EOF) has attracted wide interest in the past decade. Compared to DC EOF, AC EOF-based micropumps require lower voltage to pump uids. This can avoid the generation of microbubbles and make the devices portable. In microuidics, as early as in 2000, Green et al. 6 reported AC EOF (also known as induced-charge electroosmotic ow, ICEOF) near planar microelectrodes. By monitoring latex tracer particles, the velocity of the ow is experimentally investigated and exhibits apparent dependency on the frequency of the AC eld. On the basis of AC EOF, Studer et al. 7 designed a micropump for tunable ow control. Under very low voltages (below 10 V, rms value), a maximum ow speed of 500 μm/s can be achieved at AC electric eld of tens of kHz. In the same year, Debesset et al. 8 also designed a micropump for chromatographic application, by using AC EOF. A maximum speed of 50 μm/s was realized. Although the ow speed was an order smaller than that observed by Studer et al., 7 they successfully found that in the investigated parametric region, the ow speed of micropump had approximately linear relation with applied AC voltage and frequency. Later, in 2005, Gagnon and Chang 9 combined an AC EOF with a dielectrophoretic (DEP) ow to achieve fast bacteria detection. The bulk ow velocity due to the AC EOF could be up to 1000 Received: July 27, 2017 Accepted: December 19, 2017 Published: December 19, 2017 Article pubs.acs.org/ac Cite This: Anal. Chem. 2018, 90, 1652-1659 © 2017 American Chemical Society 1652 DOI: 10.1021/acs.analchem.7b02985 Anal. Chem. 2018, 90, 16521659