Hard carbons derived from green phenolic resins for Na-ion batteries

Hard carbons have become recently one of the most promising classes of anode materials for sodium ion batteries (NIBs) owing to their high specific capacity and good cycling stability. Among the precursors used to prepare hard carbon, phenolic resins are of great interest due to their high carbon yield, however, their toxicity must be overcome. In this paper, we propose a green, simple and scalable procedure to obtain phenolic resins which by pyrolysis at high temperature (>1000 °C) result in eco-friendly hard carbons with low surface area, disordered structure and high carbon yield. The influence of several synthesis parameters (type of solvent, thermopolymerization/annealing temperature and gas flow) was studied to determine the impact on both phenolic resin and hard carbon characteristics. The synthesis time (12 h-3 days) was found to depend on the used solvent whereas the carbon yield (25–35%) on the cross-linking degree which could be controlled by adjusting both thermopolymerization temperature and atmosphere. The structure of the hard carbons mainly changed with the carbonization temperature (1100–1700 °C) while the texture of the material was sensitive to most of the studied parameters. Stable reversible capacity up to 270 mAhg−1 and 100% coulombic efficiency (CE) after few cycles are obtained, demonstrating the potential for Na-ion applications

Hard carbons derived from green phenolic resins for Na-ion batteries

Hard carbons have become recently one of the most promising classes of anode materials for sodium ion batteries (NIBs) owing to their high specific capacity and good cycling stability. Among the precursors used to prepare hard carbon, phenolic resins are of great interest due to their high carbon yield, however, their toxicity must be overcome. In this paper, we propose a green, simple and scalable procedure to obtain phenolic resins which by pyrolysis at high temperature (>1000 °C) result in eco-friendly hard carbons with low surface area, disordered structure and high carbon yield. The influence of several synthesis parameters (type of solvent, thermopolymerization/annealing temperature and gas flow) was studied to determine the impact on both phenolic resin and hard carbon characteristics. The synthesis time (12 h-3 days) was found to depend on the used solvent whereas the carbon yield (25–35%) on the cross-linking degree which could be controlled by adjusting both thermopolymerization temperature and atmosphere. The structure of the hard carbons mainly changed with the carbonization temperature (1100–1700 °C) while the texture of the material was sensitive to most of the studied parameters. Stable reversible capacity up to 270 mAhg−1 and 100% coulombic efficiency (CE) after few cycles are obtained, demonstrating the potential for Na-ion applications

Facile and sustainable synthesis of nitrogen-doped polymer and carbon porous spheres

International audienceThe development of green, sustainable and simple synthesis pathways for the design of polymer and carbonaceous materials with well controlled features is of great importance for many fields of applications. Herein, we report a green synthesis method for polymer and carbon particles with well-defined shape and size. This approach involves the use of green precursors, water as solvent, no templates 10 under ambient temperature and pressure conditions, simultaneously. Green polymer resins (phloroglucinol-glyoxylic acid) and a catalyst/nitrogen source (triethylenediamine) are dissolved in water at room temperature resulting in polymer particles which by subsequent thermal treatment transforms in carbon particles. Mainly spherical carbon particles with controlled size from 500 nm to 10 µm were obtained by simply adjusting the experimental conditions, i.e., the synthesis time and the molar ratio between the precursors or solvent. In some conditions, flower-like morphology was obtained as well. The synthesis mechanism from polymer resin spheres 15 formation to their conversion into carbon sphere was determined by several techniques, i.e., 13 C NMR spectroscopy, SEM, XPS and TPD-MS (temperature programmed desorption coupled by mass spectrometer). 2

Understanding ageing mechanisms of porous carbons in non-aqueous electrolytes for supercapacitors applications

Two activated porous carbon powders with different surface functional groups content have been electrochemically polarized in tetraethylammonium tetrafluoborate (Et4NBF4) in acetonitrile electrolyte to study their ageing mechanism as supercapacitor electrodes. Temperature-programmed desorption coupled with mass spectrometry technique (TPD-MS) is used to track the change of carbon surface chemistry – surface functional groups and/or adsorption of degradation products occurring upon polarizations. A potentiostatic study of the carbons in a two-compartment cell unveil the catalytic role of water in the ageing mechanism. Combining these results with our previous work, we propose different scenarios to depict the ageing mechanisms of the two carbons. For carbon A, hydrolysis of BF4− at the positive electrode leads to carbon oxidation together with soluble poly-acetonitrile oligomer occurred from reaction between BF4• radicals and acetonitrile. Ageing mechanism is also assumed to set off with the hydrolysis of BF4− for carbon B; but, in here the formed oligomers react with acid functional groups present at the carbon surface to form a protective, passive-like layer at both positive and negative electrodes which hampers a further electrode ageing

Стратегия хирургического лечения местнораспространенных опухолей малого таза с применением эвисцераций. Сообщение1. Синдромы кишечной непроходимости, кровотечения и сдавления мочевых путей

Представлен обзор и анализ методов хирургической коррекции синдромов кишечной непроходимости, кровотечения и сдавления мочевых путей при местнораспространенных опухолях малого таза. Обобщен 10−летний опыт хирургического лечения данной патологии в Институте общей и неотложной хирургии. Приведена классификация основных методов оперативных пособий, направленных на достижение гемостаза и деривации мочи и кала.The methods of surgical correction of syndromes of intestinal obstruction, hemorrhage and urinary tract compression at local tumors of the small pelvis are reviewed and analyzed. The 10−year experience of surgical treatment for this pathology at Institute for General and Urgent Surgery is generalized. Main methods of operative treatment aimed at achievement of hemostasis and urine and feces derivation are presented

Relationship between the carbon nano-onions (CNOs) surface chemistry/defects and their capacitance in aqueous and organic electrolytes

The effect of surface functionalities on the supercapacitors performances has been highlighted often in many works. However, studies devoted to the influence of carbon defects did not gain particular attention due to the difficulty to quantify such parameter. In this context, carbon nano-onions were used as model material in order to understand the influence of the surface chemistry (nature and amount of oxygen groups) and structural defects (active surface area, ASA) on the capacitance. Different types of thermal treatments in oxidizing or reducing atmospheres allowed to finely tune the surface chemistry and the ASA as demonstrated by temperature programmed desorption coupled with mass spectrometry (TPD-MS). For the first time, the presice control of these characteristics independently one of each other allowed to highlight an important influence of the carbon defects on the capacitance in organic and aqueous electrolytes which outbalance the oxygen functional group effect

Hard carbon derived from coconut shells, walnut shells, and corn silk biomass waste exhibiting high capacity for Na-ion batteries

International audienceIn recent years, hard carbon materials have gained significant interest as anode materials for Na-ion batteries. Biomass waste is considered one of the most interesting, renewable, available, and cost-effective precursor to obtain hard carbon (HC); however, HC properties must be finely tuned to achieve performance comparable to those provided by Li-ion batteries. In this work, three biomass wastes (coconut shells, walnut shells, and corn silk) were evaluated as potential precursors for HC preparation involving a pyrolysis process and subsequent acid washing to remove the inorganic impurities. All obtained materials exhibited low and similar specific surface areas (< 10 m 2 g-1), but they presented different structures and surface functionalities. The walnut shell HC possessed a lower amount of inorganic impurities and oxygen-based functional groups compared to the coconut shell and corn silk HCs, leading to higher initial coulombic efficiency (iCE). The structural organization was higher in the case of the walnut shell HC, while the corn silk HC revealed a heterogeneous structure, combining both highly disordered carbon and localized graphitized domains. All HCs delivered high initial reversible capacities between 293 and 315 mAh g-1 at 50 mA g-1 current rate, which remained rather stable during long-term cycling. The best capacity (293 mAh g-1 after 100 charge/discharge cycles) and highest capacity retention (93%) was achieved in walnut HCs in half-cells, which could be associated with its higher sp 2 C content, better organized structure, and fewer impurities. An "adsorption-insertion" Na storage mechanism is suggested based on several techniques. The walnut HCs exhibited an attractive energy density of 279 Wh/kg when tested in full cells