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Annealing induced microstructural evolution of electrodeposited electrochromic tungsten oxide films

机译:电沉积电致变色氧化钨薄膜的退火诱导组织演变

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A significant influence of microstructure on the electrochromic and electrochemical performance characteristics of tungsten oxide (WO3) films potentiostatically electrodeposited from a peroxopolytungstic acid (PPTA) sol has been evaluated as a function of annealing temperature. Powerful probes like X-ray diffractometry (XRD), transmission electron microscopy (TEM), UV-vis spectrophotometry, multiple step chronoamperometry and cyclic voltammetry have been employed for the thin film characterization. The as-deposited and the film annealed at 60 degrees C are composed of nanosized grains with a dominant amorphous phase, as well as open structure which ensues from a nanoporous matrix. This ensures a greater number of electroactive sites and a higher reaction area thereby manifesting in electrochromic responses superior to that of the films annealed at higher temperatures. The films annealed at temperatures >= 250 degrees C are characterized by a prominent triclinic crystalline structure and a hexagonal phase co-exists at temperatures >= 400 degrees C. The deleterious effect on the electrochromic properties of the film with annealing is ascribed to the loss of porosity, densification and the increasing crystallinity and grain size. Amongst all films under investigation, the film annealed at 60 degrees C exhibits a high transmission modulation (AT similar to 68%) and coloration efficiency (eta similar to 77.6 cm(2) C-1) at lambda = 632.8 nm, charge storage capacity (Q(ins) similar to 21 MC cm(-2)), diffusion coefficient (6.08 x 10(-10) cm(2) s(-1)), fast color-bleach kinetics (t(c) similar to 275 s and t(b) similar to 12.5 s) and good electrochemical activity, as well as reversibility, for the lithium insertion-extraction process upon cycling. The remarkable potential, which the film annealed at 60 'C has, for practical "smart window" applications has been demonstrated. (c) 2005 Elsevier B.V. All rights reserved.
机译:已经评估了作为退火温度的函数的微观结构对由过氧多钨酸(PPTA)溶胶恒电位电沉积的氧化钨(WO3)膜的电致变色和电化学性能特征的重大影响。诸如X射线衍射法(XRD),透射电子显微镜(TEM),紫外可见分光光度法,多步计时电流法和循环伏安法等功能强大的探针已用于薄膜表征。沉积后的薄膜和在60摄氏度下退火的薄膜由具有主要非晶相的纳米级晶粒以及从纳米孔基质产生的开放结构组成。这确保了更多的电活性位点和更高的反应面积,从而表现出优于在更高温度下退火的膜的电致变色响应。在> = 250摄氏度的温度下退火的薄膜的特征在于突出的三斜晶晶体结构,并且在> = 400摄氏度的温度下共存六方相。退火对薄膜的电致变色性能的有害影响归因于损耗孔隙率,致密化以及结晶度和晶粒尺寸的增加。在所有正在研究的薄膜中,在60摄氏度退火的薄膜在λ= 632.8 nm时表现出高透射调制(AT类似于68%)和着色效率(eta类似于77.6 cm(2)C-1),电荷存储容量(Q(ins)类似于21 MC cm(-2)),扩散系数(6.08 x 10(-10)cm(2)s(-1)),快速的色漂动力学(t(c)类似于275 s和t(b)近似于12.5 s),并且循环时锂插入-萃取过程具有良好的电化学活性和可逆性。膜在60'C退火具有巨大的潜力,已证明可用于实际的“智能窗口”应用。 (c)2005 Elsevier B.V.保留所有权利。

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