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Ion and Molecule Transport in Nanochannels.

dc.contributor.authorCheng, Li-Jingen_US
dc.date.accessioned2008-08-25T20:56:29Z
dc.date.availableNO_RESTRICTIONen_US
dc.date.available2008-08-25T20:56:29Z
dc.date.issued2008en_US
dc.date.submitteden_US
dc.identifier.urihttps://hdl.handle.net/2027.42/60830
dc.description.abstractTransport of ions and molecules through nanochannels has been of interest due to the desire to understand the activity of biological ion channels and the prospect of exploiting the property in biomedical and chemical applications, such as molecular delivery and sensing. Nanochannels with critical dimensions comparable to Debye length exhibit surface charge-governed ion transport which is not accessible in microfluidic devices. To look into this unique phenomenon, we present our experimental and theoretical studies of the electrokinetic ion transport through sub-20 nm thick nanochannels. First we demonstrated ion current rectification in homogeneous silica nanochannels with ion concentration gradients. Depending on the polarity of the applied electric field, the uneven ion flux from the two ends can accumulate or deplete the ions in the nanochannel and results in asymmetric ionic conductances. Such rectifying effect was found to stem from the asymmetric cation-anion ratios at two ends of channel. The model elucidates the essential physics for the similar rectification effects reported previously in conical nanopores and nanofluidic diodes. Prior to this unified model, the rectifying effect in different nanofluidic devices were treated on the individual bases. In addition, we developed heterogeneous nanofluidic devices for the control of ion flow with well-defined surface charge distribution by patterning alumina and silica surfaces. Nanofluidic diodes were successfully fabricated by this method and demonstrated rectifying factor greater than 300 which is the highest reported to date. It was also found the different surface charge polarity inside and outside the nanochannel works as a parasitic diode and can affect ion transport. The finding suggests that the nano-/microchannel interface be taken into account in interpreting the physics of ion transport in nanochannels. Apart from electrokinetic transport in nanochannels, we demonstrated a directional, active molecule transport by utilizing the kinesin motor proteins immobilized in the opened nanochannels to propel microtubules along the nanochannels. Due to the physical confinement of the nanochannels, microtubules can glide over a long distance without detaching from the surface. This demonstration opens up the possibility of utilizing the biological molecules and artificial nanostructures to carry out several desired functions, e.g. chemical delivery or molecule concentration.en_US
dc.format.extent1863892 bytes
dc.format.extent1373 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_USen_US
dc.subjectNanofluidicsen_US
dc.subjectElectrokinetic Ion Transporten_US
dc.subjectIonic Rectificationen_US
dc.subjectNanochannelen_US
dc.titleIon and Molecule Transport in Nanochannels.en_US
dc.typeThesisen_US
dc.description.thesisdegreenamePhDen_US
dc.description.thesisdegreedisciplineElectrical Engineeringen_US
dc.description.thesisdegreegrantorUniversity of Michigan, Horace H. Rackham School of Graduate Studiesen_US
dc.contributor.committeememberGuo, Lingjieen_US
dc.contributor.committeememberHunt, Alan J.en_US
dc.contributor.committeememberKurabayashi, Katsuoen_US
dc.contributor.committeememberMayer, Michaelen_US
dc.subject.hlbsecondlevelElectrical Engineeringen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/60830/1/ljcheng_1.pdf
dc.owningcollnameDissertations and Theses (Ph.D. and Master's)


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