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High-surface-area mesoporous TiO2 microspheres via one-step nanoparticle self-assembly for enhanced lithium-ion storage

机译:High-surface-area介孔二氧化钛微球通过一步增强纳米粒子自组装锂离子存储

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Mesoporous TiO2 microspheres assembled from TiO2 nanoparticles with specific surface areas as high as 150 m~2 g~(-1) were synthesized via a facile one-step solvothermal reaction of titanium isopropoxide and anhydrous acetone. Aldol condensation of acetone gradually releases structural H2O, which hydrolyzes and condenses titanium isopropoxide, forming TiO2 nanocrystals. Simultaneous growth and aggregation of TiO2 nanocrystals leads to the formation of high-surface-area TiO2 microspheres under solvothermal conditions. After a low-temperature post-synthesis calcination, carbonate could be incorporated into TiO2 as a dopant with the carbon source coming from the organic byproducts during the synthesis. Carbonate doping modifies the electronic structure of TiO2 (e.g., Fermi level, E_f), and thus influences its electrochemical properties. Solid electrolyte interface (SE1) formation, which is not common for titania, could be initiated in carbonate-doped TiO2 due to elevated E_f. After removing carbonate dopants by high-temperature calcination, the mesoporous TiO2 microspheres showed much improved performance in lithium insertion and stability at various current rates, attributed to a synergistic effect of high surface area, large pore size and good anatase crystallinity.
机译:从二氧化钛介孔二氧化钛微球组装纳米粒子与比表面积高的地区150 m ~ 2 g ~(1)通过灵巧的合成一步solvothermal钛的反应异丙醇盐和无水丙酮。凝结的丙酮逐渐释放结构水,水解和凝结钛异丙醇盐,形成二氧化钛纳米晶体。同时增长和二氧化钛的聚合纳米晶体的形成high-surface-area二氧化钛微球在solvothermal条件。post-synthesis煅烧,碳酸盐纳入二氧化钛作为掺杂剂的碳源来自有机副产品在合成。二氧化钛的电子结构(例如,费米水平,E_f),因此其影响电化学性质。接口(SE1)形成,这并不常见二氧化钛,可以启动由于高架E_f carbonate-doped二氧化钛。去除碳酸盐岩高温掺杂物煅烧,介孔二氧化钛微球显示在锂大大改善了性能插入和稳定性在不同现在的速度,由于高的协同效应表面积、大孔隙大小和良好的锐钛矿结晶度。

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