An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
Pelton, R., Chen, L. & Smith, T. (2016). Environmental assessment of biorefinery co-products. NARA Final Reports. Pullman, WA. Northwest Advanced Renewables Alliance (NARA).
Nitrogen-doped porous carbon spheres have attracted great interest in diversified fields owing to their unique physical and chemical properties. However, the synthesis of nitrogen-doped porous carb...
Hollow polymer nanospheres (HPNSs) have received an increased level of attention, not only for their fundamental scientific interest, but also for technological applications. Despite a great deal of research effort, most of the current HPNSs are suffering from a poor polydispersity as well as a particle size larger than 500 nm. Here, we report the synthesis of highly monodisperse hollow microporous polystyrene nanospheres (MHMPNSs) with diameters as low as 120 nm based on a facile hypercrosslinking strategy. We utilize the rapid formation of an almost unreactive crosslinked polystyrene outer skin during the initial hypercrosslinking process, to minimize the undesired inter-sphere crosslinking. Due to the intra-sphere hypercrosslinking, the resulting MHMPNSs possess a well-developed microporous shell structure. The MHMPNSs are able to be used as potential absorbents toward organic vapors, because of their unique hollow core and microporous shell characteristics.
Both high surface areas and well‐orchestrated nanomorphologies are important for porous organic polymers (POPs). However, the two key characteristics are generally difficult to be satisfied simultaneously, because the common pore‐making procedures usually produce ill‐defined nanomorphologies or give rise to damage of precustomized nanomorphologies. Herein, a facile yet versatile stepwise crosslinking strategy for fabrication of POPs with an unusual nanomorphology‐persistent characteristic during pore‐making is reported. Polystyrene nanofibers and poly(styrene‐ co ‐divinylbenzene) nanosphere arrays are utilized as building blocks, and then transformed into nanofibrillar morphology‐persistent and ordered array morphology‐persistent POPs via stepwise crosslinking, respectively. The stepwise crosslinking strategy includes pre‐crosslinking and hypercrosslinking; the pre‐crosslinking in a carefully selected poor solvent of polystyrene forms a lowly crosslinked structure, which guarantees the stability of nanomorphology during the subsequent pore‐making via hypercrosslinking. The as‐obtained POPs can be used as precursors for novel well‐defined hyperporous carbon nanofibers and ordered carbon nanosphere arrays with excellent adsorption performances.
Abstract Aqueous Zn‐metal batteries are the most promising system for large‐scale energy storage due to their high capacity, high safety, and low cost. The Zn‐metal anode, however, suffers from continuous parasitic reactions, random dendrite growth, and sluggish kinetics in aqueous electrolytes. Herein, a high donor number solvent, tetramethylurea (TMU), is introduced as electrolyte additive to enable highly reversible Zn‐metal anode, where the TMU can 1) preferentially adsorb on the Zn surface to inhibit Zn corrosion and suppress parasitic reaction, 2) solvate with Zn 2+ and exclude the H 2 O from Zn 2+ solvation sheath to weaken water activity significantly, and 3) contribute to form an inorganic‐organic bilayer solid electrolyte interphase to enable homogeneous and rapid Zn 2+ transport kinetic for dendrite‐free Zn deposition. Benefiting from these three merits, the resulting aqueous electrolyte demonstrates a highly reversible Zn plating/stripping cycling in a Zn||Ti asymmetric cell for over 1200 cycles and in a Zn||Zn symmetric cell for over 4000 h. As a proof‐of‐concept, the aqueous Zn‐metal full cells assembled with various state‐of‐the‐art cathodes also deliver excellent cycling performance even with a 10 µm thin Zn anode, favoring the practical application.
Lithium–sulfur (Li–S) batteries has been regarded as one of the most promising next‐generation energy storage systems due to their high theoretical energy density. However, the practical application of Li–S batteries is still hindered by the unstable cathode‐electrolyte interphase and the early passivation of charge product (Li2S), leading to poor cycling stability and low S utilization. Herein, we propose an electrolyte engineering strategy using highly solvating hexamethylphosphoramide (HMPA) as a co‐solvent to elucidate the dissociation–precipitation chemistry of lithium polysulfides (LiPSs). The multimode optical spectroscopies confirm that this electrolyte engineering is able to effectively regulate the solvation of LiPSs to initiate a radical‐assisted conversion pathway and control three‐dimensional (3D) Li2S electrodeposition to boost sulfur utilization. More importantly, the dynamic evolution of cathode–electrolyte interphase, featuring with S‐/P‐containing species, is also assessed by both distribution of relaxation times technology and X‐ray photoelectron spectroscopy, which can suppress the passivation of Li2S to enhance conversion reversibility. As a proof‐of‐concept, a Li–S cell with high S loading mass of 7.75 mg cm−2 demonstrates an extremely high area capacity of 7.86 mAh cm−2 at a current density of 1.30 mA cm−2 , representing a significant advancement in promoting the development of practical high‐energy‐density Li–S batteries.
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