The safety aspect of sodium ion batteries for practical applications

Sodium-ion batteries(SIBs)with advantages of abundant resource and low cost have emerged as promising candidates for the next-generation energy storage systems.However,safety issues existing in electrolytes,anodes,and cathodes bring about frequent accidents regarding battery fires and explosions and impede the development of high-performance SIBs.Therefore,safety analysis and high-safety battery design have become prerequisites for the development of advanced energy storage systems.The reported reviews that only focus on a specific issue are difficult to provide overall guidance for building high-safety SIBs.To overcome the limitation,this review summarizes the recent research progress from the perspective of key components of SIBs for the first time and evaluates the characteristics of various improvement strategies.By orderly analyzing the root causes of safety problems associated with different components in SIBs(including electrolytes,anodes,and cathodes),corresponding improvement strategies for each component were discussed systematically.In addition,some noteworthy points and perspectives including the chain reaction between security issues and the selection of improvement strategies tailored to different needs have also been proposed.In brief,this review is designed to deepen our understanding of the SIBs safety issues and provide guidance and assistance for designing high-safety SIBs.

Surface organic modification of Fe_3O_4 nanoparticles by silane-coupling agents

Fe3O4 nanoparticles were prepared by chemistry co-precipitation and the mean crystal size was 17.9 nm measured by XRD. After it had been treated by silane-coupling agents KH570, magnetic micro-spheres dispersed in organic medium glycol were gained and the mean size of Fe3O4 nanopowders was 33.7 nm. So it can be concluded that magnetic micro-sphere is made of a few Fe3O4 crystals. Many factors of modification were researched, such as the time of ball milling, the content of Fe3O4 and the content of KH570. The modification of Fe3O4 is relative to the time of ball milling, but the dominant function is affected by the content of Fe3O4 and KH570. When the content of Fe3O4 is known, there is a suitable content of KH570. Different content of Fe3O4 will make the different suitable content of KH570, but the range of latter is less than former, which is relative to the distribution of KH570 on Fe3O4 surface or in the solution.

Surface Organic Modification of Fe_3O_4 Magnetic Nanoparticles

The surface organic modification of Fe3O4 nanoparticles with silane coupling reagent KH570 was studied. The modified and unmodified nanoparticles were characterized by FT-IR, XPS and TEM. The spectra of FT-IR and XPS revealed that KH570 was coated onto the surface of Fe3O4 nanoparticles to get Fe-O- Si bond and an organic coating layer also was formed. Fe3O4 nanoparticles were spheres partly with mean size of 18,8 nm studied by TEM, which was consistent with the result 17.9 nm calculated by Scherrer＇s equation. KH570 was adsorbed on surface and formed chemistry bond to be steric hindrance repulsion which prevented nanoparticles from reuniting. Then glycol-based Fe3O4 magnetic liquids dispersed stably was gained.

Study on the Effect of Surface Modification on the Properties of Bentonite Greases

In order to investigate the influening factors of organic modification procedure and find out connections between organic modification and the properties of bentonite greases, organic montmorillonite(OMMT) thickeners with different surfactant dosages and constituents were synthesized through intercalation reaction between sodium montmorillonite(NaM MT) and quaternary ammonium surfactants in aqueous solvents. The lubricating greases were prepared with the resulting organoclays, while the penetration and oil separation of lubricating greases were evaluated, respectively. The surface modification process of montmorillonite(MMT) was analyzed and the thickening mechanism of OMMT was discussed in this study. The experimental results showed that, with an increasing amount of surfactant, the basal spacing between the clay platelets was increasing and the structure of modifier molecules layer in the interlayer was changing from lateral bilayer to paraffin-type bilayer. The optimal properties of lubricating greases were achieved, when the structure of surfactant molecules loaded in the interlayer was the paraffin-type monolayer, which meant that the dosage of modifier was equal to 120—140 mmol/(100g). Meanwhile, it was found that the thickening performance, colloid stability, anti-wear and friction-reducing performance of lubricating greases were improved, when the surfactants were mixed with octadecyl trimethyl ammonium chloride(OTAC) and hexadecyl trimethyl ammonium chloride(HTAC). And the optimum mole ratio of two surfactants is was 1:1.

Flame Retardancy Evaluation of Nanocomposites Prepared from Sawdust and Montmorillonite Clay

Composites of montmorillonite clay and sawdust were prepared with the desired result being having new materials which burn longer than unmodified sawdust. The three forms of clay used for preparation of composites were unmodified montmorillonite, mono-ionic montmorillonite and organically modified montmorillonite. Montmorillonite clay was converted to mono-ionic clay by ion exchange with sodium using a sodium chloride solution. The mono-ionic clay was organically modified with an organic surfactant, methyl triphenyl phosphonium bromide. Nanocomposites were then prepared by combining the modified and raw forms of the clay with sawdust. The solution blending method was used to make the nanocomposites. The samples were analysed using thermogravimetric analysis and cone calorimetry. The studies showed that the nanocomposite which was made from sawdust and 1% organically modified clay had the most improved results in terms of burning time and thermal stability, as well as giving a calorific value closest to unmodified sawdust and the least amount of residue.

Multifunctional organically modified graphene with super-hydrophobicity

In order to bring graphene materials much closer to real world applications, it is imperative to have simple, efficient and eco-friendly ways to produce processable graphene derivatives. In this study, a hydrophilic low-temperature thermally functionalized graphene and its super-hydrophobic organically modified graphene derivative were fabricated. A unique structural topology was found and some of the oxygen functionalities were retained on the thermally functionalized graphene surfaces, which facilitated the subsequent highly effective organic modification reaction and led to the super-hydrophobic organically modified graphene with multi functional applications in liquid marbles and polymer nanocomposites. The organic modification reaction also restored the graphenic conjugated structure of the thermally functionalized graphene, particularly for organic modifiers having longer alkyl chains, as confirmed by various characteri- zation techniques such as electrical conductivity measurements, ultraviolet/visible spectroscopy and selected area electron diffraction. The free-standing soft liquid marble was fabricated by wrapping a water droplet with the super-hydrophobic organically modified graphene, and showed potential for use as a microreactor. As for the polymer nanocomposites, a strong interfacial adhesion is believed to exist between an organic polymer matrix and the modified graphene because of the organophilic coating formed on the graphene base, which resulted in large improvements in the thermal and mechanical properties of the polymer nanocomposites with the modified graphene, even at very low loading levels. A new avenue has therefore been opened up for large-scale production of processable graphene derivatives with various practicable applications.

The effect of organic ligand modification on protein corona formation of nanoscale metal organic frameworks

Nanoscale metal organic frameworks(NMOFs)have been widely reported in biomedical field for their unique porous structure and tunable multifunctionality.However,when administrated in vivo,the protein corona will be formed on the surface of NMOFs,significantly affecting their biodistribution,pharmacokinetics and drug release.Few studies paid attention to the protein corona formation process and its influencing factors of NMOFs.As a well-established strategy for altering structure features of NMOFs,the organic ligand modification may have effect on the protein corona formation process,which is to be investigated.In this study,the zirconium(Zr)-based UIO66 was chosen as model NMOFs,the organic ligand of which was modified with amino group(-NH_(2))or carboxyl group(-COOH)to synthesize UIO66-NH_(2)and UIO66-2COOH,respectively.Bovine serum albumin(BSA)was chosen as model protein to investigate the protein corona formation process of NMOFs.The current results showed that the-COOH modification remarkably enhanced the BSA adsorption on NMOFs while-NH_(2)slightly decreased the protein binding affinity.These differences may be ascribed to the two different dominate protein corona formation modes,i.e.,surface coating mode and porous embedded mode.The protein corona formation did not affect the crystal phase of NMOFs but increased the content ofα-helix of BSA.Ultimately,upon protein corona formation,the cellular uptake of NMOFs was significantly affected.We believe our study will provide a new research paradigm to the design and applications of NMOFs.

Feasibility of bubble surface modification for natural organic matter removal from river water using dissolved air flotation

A novel, functionalized bubble surface can be obtained in dissolved air flotation （DAF） by dosing chemicals in the saturator. In this study, different cationic chemicals were used as bubble surface modifiers, and their effects on natural organic matter （NOM） removal from river water were investigated. NOM in the samples was fractionated based on molecular weight and hydrophobicity. The disinfection byproduct formation potentials of each fraction and their removal efficiencies were also evaluated. The results showed that chitosan was the most promising bubble modifier compared with a surfactant and a synthetic polymer. Tiny bubbles in the OAF pump system facilitated the adsorption of chitosan onto microbubble surfaces. The hydrophobic NOM fraction was preferentially removed by chitosan-modified bubbles. Decreasing the recycle water pH from 7.0 to 5.5 improved the removal of hydrophilic NOM with low molecular weight. Likewise, hydrophilic organic compounds gave high dihaloacetic acid yields in raw water. An enhanced reduction of haloacetic acid precursors was obtained with recycle water at pH values of 5.5 and 4.0. The experimental results indicate that NOM fractions may interact with bubbles through different mechanisms. Positive bubble modification provides an alternative approach for OAF to enhance NOM removal.

Facile fabrication of covalent organic framework functionalized superhydrophobic porous sponges for highly efficient water/oil separation

Considering the serious environmental pollution and economic losses caused by increasing oil spills and chemical leaks,effective and eco-friendly methods of oil/water separation should be urgently developed.Herein,a facile strategy(about 20 min)was developed for integrating covalent organic framework(COF)particles with melamine sponges(MS)by covalent bonding,and then a superhydrophobic COF/MS composite(denoted OA-CP@MS)could be further obtained by following modification with a 1-octadecylamine/water dispersion.Specifically,the synthesis process was developed under a mild condition that avoids the need for sealing and high-temperature treatments.It was proven that the fabricated OA-CP@MS presented a prominent absorption capacity for various organic reagents,in which adsorption capacity of chloroform could be up to 173 g/g.Owing to its excellent chemical robustness in strong alkaline and saline environments and in various organic solvents,the prepared OACP@MS showed a great potential to perform oil/water separation in complex practical conditions.Its rapid preparation process,fluorine-free treatment,and water-based modification would extend the application of COF materials in oil/water separation.

Interfacial engineering of printable bottom back metal electrodes for full-solution processed flexible organic solar cells

Printing of metal bottom back electrodes of flexible organic solar cells（FOSCs） at low temperature is of great significance to realize the full-solution fabrication technology. However, this has been difficult to achieve because often the interfacial properties of those printed electrodes, including conductivity, roughness, work function,optical and mechanical flexibility, cannot meet the device requirement at the same time. In this work, we fabricate printed Ag and Cu bottom back cathodes by a low-temperature solution technique named polymer-assisted metal deposition（PAMD） on flexible PET substrates. Branched polyethylenimine（PEI） and ZnO thin films are used as the interface modification layers（IMLs） of these cathodes. Detailed experimental studies on the electrical, mechanical, and morphological properties, and simulation study on the optical properties of these IMLs are carried out to understand and optimize the interface of printed cathodes. We demonstrate that the highest power conversion efficiency over 3.0% can be achieved from a full-solution processed OFSC with the device structure being PAMDAg/PEI/P3 HT：PC61BM/PH1000. This device also acquires remarkable stability upon repeating bending tests.