Giannuzzi Roberto, Manca Michele, De Marco Luisa, Belviso Maria R, Cannavale Alessandro, Sibillano Teresa, Giannini Cinzia, Cozzoli P Davide, Gigli Giuseppe
Center for Bio-Molecular Nanotechnology, Fondazione Istituto Italiano di Tecnologia , Via Barsanti, 73010 Arnesano, Lecce, Italy.
ACS Appl Mater Interfaces. 2014 Feb 12;6(3):1933-43. doi: 10.1021/am4049833. Epub 2014 Jan 17.
The peculiar architecture of a novel class of anisotropic TiO2(B) nanocrystals, which were synthesized by an surfactant-assisted nonaqueous sol-gel route, was profitably exploited to fabricate highly efficient mesoporous electrodes for Li storage. These electrodes are composed of a continuous spongy network of interconnected nanoscale units with a rod-shaped profile that terminates into one or two bulgelike or branch-shaped apexes spanning areas of about 5 × 10 nm(2). This architecture transcribes into a superior cycling performance (a charge capacitance of 222 mAh g(-1) was achieved by a carbon-free TiO2(B)-nanorods-based electrode vs 110 mAh g(-1) exhibited by a comparable TiO2-anatase electrode) and good chemical stability (more than 90% of the initial capacity remains after 100 charging/discharging cycles). Their outstanding lithiation/delithiation capabilities were also exploited to fabricate electrochromic devices that revealed an excellent coloration efficiency (130 cm(2) C(-1) at 800 nm) upon the application of 1.5 V as well as an extremely fast electrochromic switching (coloration time ∼5 s).
通过表面活性剂辅助的非水溶胶-凝胶法合成了一类新型各向异性TiO₂(B)纳米晶体,其独特的结构被成功用于制备高效的锂存储介孔电极。这些电极由相互连接的纳米级单元组成的连续海绵状网络构成,呈棒状外形,末端为一个或两个凸起状或分支状顶点,跨越面积约为5×10 nm² 。这种结构转化为优异的循环性能(基于无碳TiO₂(B)纳米棒的电极实现了222 mAh g⁻¹ 的充电电容,而类似的TiO₂锐钛矿电极的充电电容为110 mAh g⁻¹ )和良好的化学稳定性(100次充放电循环后仍保留超过90%的初始容量)。它们出色的锂化/脱锂能力还被用于制造电致变色器件,该器件在施加1.5 V电压时显示出优异的着色效率(800 nm处为130 cm² C⁻¹ )以及极快的电致变色切换速度(着色时间约为5 s)。