Thermal Conductivity of Carbon Nanotubes and their Polymer Nanocomposites: A Review

Thermally conductive polymer composites offer new possibilities for replacing metal parts in several applications, including power electronics, electric motors and generators, heat exchangers, etc., thanks to the polymer advantages such as light weight, corrosion resistance and ease of processing. Current interest to improve the thermal conductivity of polymers is focused on the selective addition of nanofillers with high thermal conductivity. Unusually high thermal conductivity makes carbon nanotube (CNT) the best promising candidate material for thermally conductive composites. However, the thermal conductivities of polymer/CNT nanocomposites are relatively low compared with expectations from the intrinsic thermal conductivity of CNTs. The challenge primarily comes from the large interfacial thermal resistance between the CNT and the surrounding polymer matrix, which hinders the transfer of phonon dominating heat conduction in polymer and CNT. This article reviews the status of worldwide research in the thermal conductivity of CNTs and their polymer nanocomposites. The dependence of thermal conductivity of nanotubes on the atomic structure, the tube size, the morphology, the defect and the purification is reviewed. The roles of particle/polymer and particle/particle interfaces on the thermal conductivity of polymer/CNT nanocomposites are discussed in detail, as well as the relationship between the thermal conductivity and the micro- and nano-structure of the composite

Reduction of Grain Boundary Resistance of La0.5Li0.5TiO3 by the Addition of Organic Polymers

The organic solvents that are widely used as electrolytes in lithium ion batteries present safety challenges due to their volatile and flammable nature. The replacement of liquid organic electrolytes by non-volatile and intrinsically safe ceramic solid electrolytes is an effective approach to address the safety issue. However, the high total resistance (bulk and grain boundary) of such compounds, especially at low temperatures, makes those solid electrolyte systems unpractical for many applications where high power and low temperature performance are required. The addition of small quantities of a polymer is an efficient and low cost approach to reduce the grain boundary resistance of inorganic solid electrolytes. Therefore, in this work, we study the ionic conductivity of different composites based on non-sintered lithium lanthanum titanium oxide (La0.5Li0.5TiO3) as inorganic ceramic material and organic polymers with different characteristics, added in low percentage (<15 wt.%). The proposed cheap composite solid electrolytes double the ionic conductivity of the less cost-effective sintered La0.5Li0.5TiO3.We thank the Spanish Ministry for Science and Technology (MAT2007-64486-C07-05) and CDTI (ALMAGRID of the "CERVERA Centros Tecnológicos" program, CER-20191006) for financial their support. JS, AV, SG, and FG also want to acknowledge Agencia Española de Investigación /Fondo Europeo de Desarrollo Regional (FEDER/UE) for funding the projects PID2019-106662RB-C41, C42, C43, and C44

Computer simulations of single-ion BAB triblock copolymer electrolyte material for Lithium-polymer batteries

http://tartu.ester.ee/record=b2693136~S1*es

Characterization of polyether-poly(methyl methacrylate)-lithium perchlorate blend electrolytes

Em publicaçãoSolid polymer electrolytes (SPEs) systems based on interpenetrating blends of poly(ethylene oxide-co-propylene oxide) and poly(methyl methacrylate) host matrices, with lithium perchlorate as guest salt, were prepared. These electrolytes were presented as free-standing films, and their thermal and electrochemical properties were characterized by conductivity and electrochemical stability measurements. The properties of the interpenetrating blends of poly(ethylene oxide-co-propylene oxide) and poly(methyl methacrylate) host matrices as the electrolyte component of a solid-state electrochromic device are reported and the results obtained suggest that this electrolyte provides an encouraging performance in this application. The most conducting electrolyte composition of this SPE system is the formulation designated as SPE2-0PC (5.01x10-4 S cm-1 at about 57ºC). The lowest decomposition temperature was registered with the SPE6-15PC composition (233ºC). The average transmittance in the visible region of the spectrum was above 41% for all the samples analyzed. After coloration the device assembled with 71 wt% PC presented an average transmittance of 15.71% and an optical density at 550nm of 0.61.Fundação para a Ciência e a Tecnologia (FCT

Measurement of Three Transport Coefficients and the Thermodynamic Factor in Block Copolymer Electrolytes with Different Morphologies.

The design and engineering of composite materials is one strategy to satisfy the materials needs of systems with multiple orthogonal property requirements. In the case of rechargeable batteries with lithium metal anodes, the system requires a separator with fast lithium ion transport and good mechanical strength. In this work, we focus on the system polystyrene-block-poly(ethylene oxide) (SEO) with bis(trifluoromethane)sulfonimide lithium salt (LiTFSI). Ion transport occurs in the salt-containing poly(ethylene oxide)-rich domains. Mechanical rigidity arises due to the glassy nature of polystyrene (PS). If we assume that the salt does not interact with the PS-rich domains, we can describe ion transport in the electrolyte by three transport parameters (ionic conductivity, κ, salt diffusion coefficient, D, and cation transference number, t+0) and a thermodynamic factor, Tf. By systematically varying the volume fraction of the conducting phase, ϕc between 0.29 and 1.0, and chain length, N between 80 and 8000, we elucidate the role of morphology on ion transport. We find that κ is the strongest function of morphology, varying by three full orders of magnitude, while D is a weaker function of morphology. To calculate t+0 and Tf, we measure the current fraction, ρ+, and the open circuit potential, U, of concentration cells. We find that ρ+ and U follow universal trends as a function of salt concentration, regardless of chain length, morphology, or ϕc, allowing us to calculate t+0 for any SEO/LiTFSI or PEO/LiTFSI mixture when κ and D are known. The framework developed in this paper enables predicting the performance of any block copolymer electrolyte in a rechargeable battery

Printing 3D lithium-ion microbattery using stereolithography

Microbatteries have been gained a lot of importance since the development of micro- and nanotechnologies. Integrating the microbattery system will enable a variety of applications, such as implantable biomedical devices and wireless sensor networks. In this paper, we demonstrated a new method to fabricate three dimensional lithium-ion microbattery using stereolithiography. A UV-curable gel polymer electrolyte resin is first synthesized and characterized. The electrolyte resin is then applied to build into 3D architecture by stereolithography. The gel electrolyte structure is designed into a zigzag shape in order to improve the contact area between electrode and electrolyte. Battery\u27s active material, LiFePO4 (LFP) and Li4Ti5 O12 (LTO), are mixed with the gel electrolyte resin and then flow into the gel electrolyte structure. The result demonstrates a feasibility of lithium-ion microbattery fabricated by stereolithgraphy