二氧化钒纳米结构的水热合成、光谱、光学和电化学表征

Meenu, Bharti, B. S. Dehiya
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引用次数: 1

摘要

以V2O5为钒源,2 -羟基丙烷-1,2,3-三羧酸为还原剂和结构导向剂,在230℃条件下,通过一步水热法成功合成了VO2(B)。通过x射线衍射(XRD)和扫描电镜(SEM)对产物化合物进行了分析,并用FTIR和UV-VIS光谱对其理化性质进行了表征。所制得的纳米VO2 (B)在10nm以下,光学带隙为2.67eV。在ITO衬底上沉积了VO2 (B)纳米颗粒薄膜,并用循环伏安法对其进行了电化学表征。电化学表征表明,该材料具有可逆的氧化还原行为,符合锂的可逆插/脱插过程。以钒源V2O5为原料,2 -羟基丙烷-1,2,3-三羧酸为还原剂和结构导向剂,在230℃条件下,通过一步水热法成功合成了vo2 (B)。通过x射线衍射(XRD)和扫描电镜(SEM)对产物化合物进行了分析,并用FTIR和UV-VIS光谱对其理化性质进行了表征。所制得的纳米VO2 (B)在10nm以下,光学带隙为2.67eV。在ITO衬底上沉积了VO2 (B)纳米颗粒薄膜,并用循环伏安法对其进行了电化学表征。电化学表征显示出可逆的氧化还原行为,对应于可逆的锂嵌入/脱嵌。
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Hydrothermal synthesis, spectroscopic, optical and electrochemical characterization of vanadium dioxide nanostructures
VO2(B) has been successfully synthesized via one step hydrothermal process using vanadium source as V2O5 and 2-Hydroxypropane-1,2,3-tricarboxylic acid as reducing and structure directing agent at 230°C for 24 hr. The product compound was analysed through X-ray diffraction (XRD) and scanning electron microscopy (SEM), and its physicochemical properties are characterized by FTIR and UV-VIS spectroscopy. The obtained VO2 (B) nanoparticles are under 10nm with optical band gap of 2.67eV. Thin film of VO2 (B) nanoparticles was deposited on ITO substrate was electrochemically characterized by cyclic voltammetry. The electrochemical characterizations have revealed reversible redox behavior which corresponds to the reversible lithium intercalation/deintercalation.VO2(B) has been successfully synthesized via one step hydrothermal process using vanadium source as V2O5 and 2-Hydroxypropane-1,2,3-tricarboxylic acid as reducing and structure directing agent at 230°C for 24 hr. The product compound was analysed through X-ray diffraction (XRD) and scanning electron microscopy (SEM), and its physicochemical properties are characterized by FTIR and UV-VIS spectroscopy. The obtained VO2 (B) nanoparticles are under 10nm with optical band gap of 2.67eV. Thin film of VO2 (B) nanoparticles was deposited on ITO substrate was electrochemically characterized by cyclic voltammetry. The electrochemical characterizations have revealed reversible redox behavior which corresponds to the reversible lithium intercalation/deintercalation.
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