91 research outputs found
From High to Low Temperature The Revival of Sodium Beta Alumina for Sodium Solid State Batteries
Sodium based batteries are promising post lithium ion technologies because sodium offers a specific capacity of 1166 amp; 8197;mAh amp; 8201;g amp; 8722;1 and a potential of amp; 8722;2.71 amp; 8197;V vs. the standard hydrogen electrode. The solid electrolyte sodium beta alumina shows a unique combination of properties because it exhibits high ionic conductivity, as well as mechanical stability and chemical stability against sodium. Pairing a sodium negative electrode and sodium beta alumina with Na ion type positive electrodes, therefore, results in a promising solid state cell concept. This review highlights the opportunities and challenges of using sodium beta alumina in batteries operating from medium to low temperatures 200 amp; 8201; C 20 amp; 8201; C . Firstly, the recent progress in sodium beta alumina fabrication and doping methods are summarized. We discuss strategies for modifying the interfaces between sodium beta alumina and both the positive and negative electrodes. Secondly, recent achievements in designing full cells with sodium beta alumina are summarized and compared. The review concludes with an outlook on future research directions. Overall, this review shows the promising prospects of using sodium beta alumina for the development of solid state batterie
Assessment on the Use of High Capacity “SnP”/NHC Composite Electrodes for Sodium-Ion Batteries with Ether and Carbonate Electrolytes
This work reports the facile synthesis of a Sn–P composite combined with nitrogen doped hard carbon (NHC) obtained by ball-milling and its use as electrode material for sodium ion batteries (SIBs). The “SnP”/NHC electrode (with nominal composition “SnP”:NHC = 75:25 wt%) when coupled with a diglyme-based electrolyte rather than the most commonly employed carbonate-based systems, exhibits a reversible capacity of 550 mAh g at 50 mA g and 440 mAh g over 500 cycles (83% capacity retention). Morphology and solid electrolyte interphase formation of cycled “SnP”/NHC electrodes is studied via electron microscopy and X-ray photoelectron spectroscopy. The expansion of the electrode upon sodiation (300 mAh g) is only about 12–14% as determined by in situ electrochemical dilatometry, giving a reasonable explanation for the excellent cycle life despite the conversion-type storage mechanism. In situ X-ray diffraction shows that the discharge product is NaSn. The formation of mostly amorphous NaP is derived from the overall (electro)chemical reactions. Upon charge the formation of Sn is observed while amorphous P is derived, which are reversibly alloying with Na in the subsequent cycles. However, the formation of SnP can be certainly excluded
Co Intercalation Batteries CoIBs Role of TiS2 as Electrode for Storing Solvated Na Ions
The co intercalation of solvent molecules along with Na into the crystal lattice of electrode materials is an undesired process in sodium batteries. An exception is the intercalation of ether solvated alkali ions into graphite, a fast and highly reversible process. Here, reversible co intercalation is shown to also be possible for other layered materials, namely titanium disulfide. Operando X ray diffraction and dilatometry are used to demonstrate different storage mechanisms for different electrolyte solvents. Diglyme is found to co intercalate into the TiS2 leading to a change in the voltage profile and an increase in the interlayer spacing amp; 8776;150 . This behavior is different compared to other solvents, which expand much less during Na storage 24 for tetrahydrofuran [THF] and for a carbonate mixture . For all solvents, specific capacities 2nd cycle exceed 250 mAh g amp; 8722;1 whereas THF exhibited the best stability after 100 cycles. The solvent co intercalation is rationalized by density functional theory and linked to the stability of the solvation shells, which is largest for diglyme. Finally, the TiS2 electrode with diglyme electrolyte is paired with a graphite electrode to realize the first proof of concept solvent co intercalation battery, that is, a battery with two electrodes that both rely on reversible co intercalation of solvent molecule
Analysis of large oxygenated and nitrated polycyclic aromatic hydrocarbons formed under simulated diesel engine exhaust conditions (by compound fingerprints with SPE/LC-API-MS)
The analysis of organic compounds in combustion exhaust particles and the chemical transformation of soot by nitrogen oxides are key aspects of assessment and mitigation of the climate and health effects of aerosol emissions from fossil fuel combustion and biomass burning. In this study we present experimental and analytical techniques for efficient investigation of oxygenated and nitrated derivatives of large polycyclic aromatic hydrocarbons (PAHs), which can be regarded as well-defined soot model substances. For coronene and hexabenzocoronene exposed to nitrogen dioxide under simulated diesel exhaust conditions, several reaction products with high molecular mass could be characterized by liquid chromatography-atmospheric pressure chemical (and photo) ionization-mass spectrometry (LC-APCI-MS and LC-APPI-MS). The main products of coronene contained odd numbers of nitrogen atoms (m/z 282, 256, 338), whereas one of the main products of hexabenzocoronene exhibited an even number of nitrogen atoms (m/z 391). Various reaction products containing carbonyl and nitro groups could be tentatively identified by combining chromatographic and mass spectrometric information, and changes of their relative abundance were observed to depend on the reaction conditions. This analytical strategy should highlight a relatively young technique for the characterization of various soot-contained, semi-volatile, and semi-polar reaction products of large PAHs
Photoacoustic Experimental System To Confirm Infrared Absorption Due to Greenhouse Gases
An experimental system for detecting infrared absorption using the photoacoustic (PA) effect is described. It is aimed for use at high-school level to illustrate the difference in infrared (IR) absorption among the gases contained in the atmosphere in connection with the greenhouse effect. The experimental system can be built with readily available components and is suitable for small-group experiments. The PA signal from a greenhouse gas (GHG), such as CO2, H2O, and CH4, can be detected down to a concentration of 0.1%. Since the basic theory of the PA effect in gases due to IR absorption is straightforward, the experiments with this PA system are accessible to students. It can be shown that there is a significant difference in IR absorption between GHGs and the major components of the atmosphere, N2, O2, and Ar, which helps students understand that the minor components, that is, the GHGs, determine the IR absorptivity of the atmosphere
Metal hydrides for concentrating solar thermal power energy storage
The development of alternative methods for thermal energy storage is important for improving the efficiency and decreasing the cost for Concentrating Solar-thermal Power (CSP). We focus on the underlying technology that allows metal hydrides to function as Thermal Energy Storage (TES) systems and highlight the current state-of-the-art materials that can operate at temperatures as low as room-temperature and as high as 1100 oC. The potential of metal hydrides for thermal storage is explored while current knowledge gaps about hydride properties, such as hydride thermodynamics, intrinsic kinetics and cyclic stability, are identified. The engineering challenges associated with utilising metal hydrides for high-temperature thermal energy storage are also addressed
The Molecular Identification of Organic Compounds in the Atmosphere: State of the Art and Challenges
Purity and radioactive decay behaviour of industrial 2D-reinforced SiCf/SiC composites
Ceramic matrix composites based on SiC with continuous fibres (SiCf/SiC) are considered promising structural materials for future fusion devices. It was still to clarify, whether impurities in industrial SiCf/SiC could jeopardise radiological advantages. Experimental impurity analyses revealed a two-dimensionally reinforced SiCf/SiC with the matrix produced by \CVI\ as very pure. Chemo-spectrometric methods were combined with radioactivation methods (CPAA, NAA). A quantification of the main constituents Si, C and O was added. Calculations with the FISPACT-2.4 code and EAF-2 library identified elements detrimental for different low-activation criteria. For the neutron exposure, \EEF\ reactor-study first wall and blanket conditions were simulated. The calculated SiCf/ SiC included 48 trace elements. Even under conservative assumptions, all low-activation limits of European interest are fulfilled. Exclusively the hands-on recycling limit for the First Wall can intrinsically not be satisfied with SiC. The theoretical goal of a SiCf/SiC depleted of 28Si (isotopic tailoring) is critically discussed
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