Over the past 30 years, significant commercial and academic progress has been made on Li-based battery technologies. From the early Li-metal anode iterations to the current commercial Li-ion batteries (LIBs), the story of the Li-based battery is full of breakthroughs and back tracing steps. This review will discuss the main roles of material science in the development of LIBs. As LIB research progresses and the materials of interest change, different emphases on the different subdisciplines of material science are placed. Early works on LIBs focus more on solid state physics whereas near the end of the 20th century, researchers began to focus more on the morphological aspects (surface coating, porosity, size, and shape) of electrode materials. While it is easy to point out which specific cathode and anode materials are currently good candidates for the next-generation of batteries, it is difficult to explain exactly why those are chosen. In this review, for the reader a complete developmental story of LIB should be clearly drawn, along with an explanation of the reasons responsible for the various technological shifts. The review will end with a statement of caution for the current modern battery research along with a brief discussion on beyond lithium-ion battery chemistries.

30 Years of Lithium-Ion Batteries.

http://staff.ulsu.ru/moliver/ref/polymers/pott11.pdf

Graphene-based polymer nanocomposites

There have been a number of review papers on layered silicate and carbon nanotube reinforced polymer nanocomposites, in which the fillers have high aspect ratios. Particulate–polymer nanocomposites containing fillers with small aspect ratios are also an important class of polymer composites. However, they have been apparently overlooked. Thus, in this paper, detailed discussions on the effects of particle size, particle/matrix interface adhesion and particle loading on the stiffness, strength and toughness of such particulate–polymer composites are reviewed. To develop high performance particulate composites, it is necessary to have some basic understanding of the stiffening, strengthening and toughening mechanisms of these composites. A critical evaluation of published experimental results in comparison with theoretical models is given.

/pdf/effects-of-particle-size-particle-matrix-interface-adhesion-yv055zq7xi.pdf

Effects of particle size, particle/matrix interface adhesion and particle loading on mechanical properties of particulate–polymer composites

Surface modification of inorganic nanoparticles for development of organic–inorganic nanocomposites—A review

Recently, polymer nanocomposites reinforced with lower volume fraction of nanoceramics and carbon nanotubes have attracted steadily growing interest due to their peculiar and fascinating properties as well as their unique applications in commercial sectors. The incorporation of nanoceramics such as layered silicate clays, calcium carbonate or silica nanoparticles arranged on the nanometer scale with a high aspect ratio and/or an extremely large surface area into polymers improves their mechanical performances significantly. The properties of nanocomposites depend greatly on the chemistry of polymer matrices, nature of nanofillers, and the way in which they are prepared. The uniform dispersion of nanofillers in the polymer matrices is a general prerequisite for achieving desired mechanical and physical characteristics. In this review article, current development on the processing, structure, and mechanical properties of polymer nanocomposites reinforced with respective layered silicates, ceramic nanoparticles and carbon nanotubes will be addressed. Particular attention is paid on the structure–property relationship of such novel high-performance polymer nanocomposites.

Structural and mechanical properties of polymer nanocomposites

Provided is a nano titanium dioxide composite particle and a preparation method thereof. An organic titanium source, a Pt salt and a Co salt are used as precursors and dissolved in an ethanol solvent. By using a spray pyrolysis process, the precursors in the form of an atomized diffusion gas are sprayed into a reactor through a feeder. In an auxiliary flame of hydrogen and oxygen, the atomized precursors react to form sub-nanometer, platinum-loaded titanium dioxide composite particles. The size of the composite particles is 10-30 nm. The mass of platinum is 0.5-2% of the mass of titanium dioxide. The sub-nanometer platinum has a size of 0.5 to 1.2 nm and is uniformly supported on the surface of the titanium dioxide composite particles. The method increases the nucleation rate of platinum by introducing a cobalt source, reduces the particle size of platinum, and obtains Pt-loaded particles having a high loading amount and a sub-nanometer size.

Nano titanium dioxide composite particle and preparation method thereof

The present study successfully produced a highly effective and stable organ phosphorus-doped tungsten trioxide (P-WO3) photocatalyst by a combination of hydrothermal and postcalcination methods. The crystallites, morphologies, and optical properties of the produced WO3 and P-WO3 crystals were investigated. The results indicated that P was consistently doped into the WO3 lattice in a pentavalent-oxidation state (P5+). Additionally, charge carrier traps capable of accepting photoelectrons were created. Additionally, the optical band gap was reduced from 2.4 to 2.33 eV. The degradation of methyl blue by photocatalysts was utilized to evaluate the photocatalytic performance of the synthesized P-WO3 samples at varied P concentrations (MB). The sample containing 6% -P-WO3 exhibited the best photocatalytic performance, degrading 96 percent of MB in 120 minutes, which was more than four times faster than the pure WO3 sample. The practicality of the synthesized P-WO3 was determined using samples from two residential wastewater treatment plants. When treating real wastewater with low organic matter concentrations, the P-WO3 demonstrated strong photodegradation performance. The creation of hydroxyl radicals (OH) and photography-created holes (h+) could be the key protagonists of photocatalytic activity in the P-WO3.

Ling Zhang

Papers

Nano titanium dioxide composite particle and preparation method thereof

Photocatalytic Performance Study of Organophosphorus-Doped Tungsten Trioxide and Composite Materials