Publications by authors named "Krysten Minnici"

While the focus of research related to the design of robust, high-performance Li-ion batteries relates primarily to the synthesis of active particles, the binder plays a crucial role in stability and ensures electrode integrity during volume changes that occur with cycling. Conventional polymeric binders such as poly(vinylidene difluoride) generally do not interact with active particle surfaces and fail to accommodate large changes in particle spacing during cycling. Thus, attention is now turning toward the exploration of interfacial interactions between composite electrode constituents as a key element in ensuring electrode stability.

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Rational design and construction of effective silicon (Si) electrode structures to relieve large volumetric changes that occur during the charge/discharge process remain significant challenges for the development of robust lithium-ion batteries (LIBs). Herein, we propose an electrically conductive poly[3-(potassium-4-butanoate)thiophene] (PPBT) capping layer on the Si surface (Si@PPBT) to serve as the active material and be used in conjunction with a common polymer binder as an approach to tackle issues emanating from volumetric changes. The PPBT protective shell layer provides the system with tolerance toward variations in active material volume during cycling, improves the dispersion of Si nanoparticles in the binder, enhances the electrolyte uptake rate, and provides a strong adhesion force between the Si/carbon additives/current collector, thereby helping to maintain electrode integrity during the charge/discharge process.

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Conjugated polymers possessing polar functionalities were shown to effectively anchor single-walled carbon nanotubes (SWNTs) to the surface of high-capacity anode materials and enable the formation of electrical networks. Specifically, poly[3-(potassium-4-butanoate) thiophene] (PPBT) served as a bridge between SWNT networks and various anode materials, including monodispersed FeO spheres (sFeO) and silicon nanoparticles (Si NPs). The PPBT π-conjugated backbone and carboxylate (COO-) substituted alkyl side chains, respectively, attracted the SWNT π-electron surface and chemically interacted with active material surface hydroxyl (-OH) species to form a carboxylate bond.

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A carbon nanotube (CNT) web electrode comprising magnetite spheres and few-walled carbon nanotubes (FWNTs) linked by the carboxylated conjugated polymer, poly[3-(potassium-4-butanoate) thiophene] (PPBT), was designed to demonstrate benefits derived from the rational consideration of electron/ion transport coupled with the surface chemistry of the electrode materials components. To maximize transport properties, the approach introduces monodispersed spherical FeO (sFeO) for uniform Li diffusion and a FWNT web electrode frame that affords characteristics of long-ranged electronic pathways and porous networks. The sFeO particles were used as a model high-capacity energy active material, owing to their well-defined chemistry with surface hydroxyl (-OH) functionalities that provide for facile detection of molecular interactions.

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