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Martin Z. Bazant. Chu, Kevin Taylor Massachusetts Institute of Technology. Dept. of Mathematics. Massachusetts Institute of Technology. Department of Mathematics 2006-07-31T15:21:59Z 2006-07-31T15:21:59Z 2005 2005 http://hdl.handle.net/1721.1/33669 64565040 Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Mathematics, 2005. Includes bibliographical references (p. 237-244). In the study of electrochemical transport processes, experimental exploration currently outpaces theoretical understanding of new phenomena. Classical electrochemical transport theory is not equipped to explain the behavior of electrochemical systems in the extreme operating conditions required by modern devices. In this thesis, we extend the classical theory to examine the response of two electrochemical systems that form the basis for novel electrochemical devices. We first examine the DC response of an electrochemical thin film, such as the separator in a micro-battery, driven by current applied through reactive electrodes. The model system consists of a binary electrolyte between parallel-plate electrodes, each possessing a compact Stern layer which mediates Faradaic reactions with Butler-Volmer kinetics. Our analysis differs from previous studies in two significant ways. First, we impose the full nonlinear, reactive boundary conditions appropriate for electrolytic/galvanic cells. (cont.) Since surface effects become important for physically small systems, the use of reactive boundary conditions is critical in order to gain insight into the behavior of actual electrochemical thin films that are sandwiched between reactive electrodes, especially at high current densities. For instance, our analysis shows that reaction rate constants and the Stern-layer capacitance have a strong influence on the response of the thin film. Second, we analyze the system at high current densities (far beyond the classical diffusion-limited current) which may be important for high power-density applications. At high currents, we obtain previously unknown characterizations of two interesting features at the cathode end of the cell: (i) a nested boundary layer structure and (ii) an extended space charge region. Next, we study the response of a metal (i.e., polarizable) colloid sphere in an electrolyte solution over a range of applied electric fields. (cont.) This problem, which underlies novel electrokinetically driven microfluidic devices, has traditionally been analyzed using circuit models which neglect bulk concentration variations that arise due to double layer charging. Our analysis, in contrast, is based on the Nernst-Planck equations which explicitly allow for bulk concentration gradients. A key feature of our analysis is the use of surface conservation laws to provide effective boundary conditions that couple the double layer charging dynamics, surface transport processes, and bulk transport processes. The formulation and derivation of these surface conservation laws via boundary layer analysis is one of the main contributions of this thesis. For steady applied fields, our analysis shows that bulk concentrations gradients become significant at high applied fields and affect both bulk and double layer transport processes. We also find that surface transport becomes important for strong applied fields as a result of enhanced absorption of ions by the double layer. (cont.) Unlike existing theoretical studies which focus on weak applied fields (so that both of these effects remain weak), we explore the response of the system to strong applied fields where both bulk concentration gradients and surface transport contribute at leading order. For the unsteady problem at applied fields that are not too strong, we find that diffusion processes, which are necessary for the system to relax to steady-state, are suppressed at leading-order but appear as higher-order corrections. This result is derived in a novel way using time-dependent matched asymptotic analysis. Unfortunately, the dynamic response of the system to large applied fields seems to introduce several complications that make the analysis (both mathematical and numerical) quite challenging; the resolution of these challenges is left for future work. Both of these problems require the use of novel techniques of asymptotic analysis (e.g., multiple parameter asymptotic expansions, surface conservation laws, and time-dependent asymptotic matching) and advanced numerical methods (e.g., pseudospectral methods, Newton-Kantorovich method, and direct matrix calculation of Jacobians) which may be applicable elsewhere. by Kevin Taylor Chu. Ph.D. 244 p. 11555675 bytes 11566560 bytes application/pdf application/pdf eng Massachusetts Institute of Technology M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 Mathematics. Asymptotic analysis of extreme electrochemical transport Thesis application/pdf false Publication unknown unknown <Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="0047efd7-28cf-4e27-a174-2e3dd4010790"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>Asymptotic analysis of extreme electrochemical transport</Title> <PublishedIn> <Publication> </Publication> </PublishedIn> <PublicationDate>2005</PublicationDate> <Authors> <Author> <DisplayName>Chu, Kevin Taylor</DisplayName> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>Massachusetts Institute of Technology</DisplayName> <OrgUnit /> </Publisher> </Publishers> <License>http://dspace.mit.edu/handle/1721.1/7582</License> <Keyword>Mathematics.</Keyword> <Abstract>In the study of electrochemical transport processes, experimental exploration currently outpaces theoretical understanding of new phenomena. Classical electrochemical transport theory is not equipped to explain the behavior of electrochemical systems in the extreme operating conditions required by modern devices. In this thesis, we extend the classical theory to examine the response of two electrochemical systems that form the basis for novel electrochemical devices. We first examine the DC response of an electrochemical thin film, such as the separator in a micro-battery, driven by current applied through reactive electrodes. The model system consists of a binary electrolyte between parallel-plate electrodes, each possessing a compact Stern layer which mediates Faradaic reactions with Butler-Volmer kinetics. Our analysis differs from previous studies in two significant ways. First, we impose the full nonlinear, reactive boundary conditions appropriate for electrolytic/galvanic cells.</Abstract> <Abstract>(cont.) Since surface effects become important for physically small systems, the use of reactive boundary conditions is critical in order to gain insight into the behavior of actual electrochemical thin films that are sandwiched between reactive electrodes, especially at high current densities. For instance, our analysis shows that reaction rate constants and the Stern-layer capacitance have a strong influence on the response of the thin film. Second, we analyze the system at high current densities (far beyond the classical diffusion-limited current) which may be important for high power-density applications. At high currents, we obtain previously unknown characterizations of two interesting features at the cathode end of the cell: (i) a nested boundary layer structure and (ii) an extended space charge region. Next, we study the response of a metal (i.e., polarizable) colloid sphere in an electrolyte solution over a range of applied electric fields.</Abstract> <Abstract>(cont.) This problem, which underlies novel electrokinetically driven microfluidic devices, has traditionally been analyzed using circuit models which neglect bulk concentration variations that arise due to double layer charging. Our analysis, in contrast, is based on the Nernst-Planck equations which explicitly allow for bulk concentration gradients. A key feature of our analysis is the use of surface conservation laws to provide effective boundary conditions that couple the double layer charging dynamics, surface transport processes, and bulk transport processes. The formulation and derivation of these surface conservation laws via boundary layer analysis is one of the main contributions of this thesis. For steady applied fields, our analysis shows that bulk concentrations gradients become significant at high applied fields and affect both bulk and double layer transport processes. We also find that surface transport becomes important for strong applied fields as a result of enhanced absorption of ions by the double layer.</Abstract> <Abstract>(cont.) Unlike existing theoretical studies which focus on weak applied fields (so that both of these effects remain weak), we explore the response of the system to strong applied fields where both bulk concentration gradients and surface transport contribute at leading order. For the unsteady problem at applied fields that are not too strong, we find that diffusion processes, which are necessary for the system to relax to steady-state, are suppressed at leading-order but appear as higher-order corrections. This result is derived in a novel way using time-dependent matched asymptotic analysis. Unfortunately, the dynamic response of the system to large applied fields seems to introduce several complications that make the analysis (both mathematical and numerical) quite challenging; the resolution of these challenges is left for future work. Both of these problems require the use of novel techniques of asymptotic analysis (e.g., multiple parameter asymptotic expansions, surface conservation laws, and time-dependent asymptotic matching) and advanced numerical methods (e.g., pseudospectral methods, Newton-Kantorovich method, and direct matrix calculation of Jacobians) which may be applicable elsewhere.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication>