Thickness-regulated sol-gel Bi₂O₃ thin films with black-brown electrochromic coloration for visual energy-storage electrodes
编号:50 访问权限:仅限参会人 更新:2026-10-20 23:49:27 浏览:92次 口头报告

报告开始:2026年10月27日 17:20(Asia/Shanghai)

报告时间:10min

所在会场:[D2] Tuesday 27 October 2026 [S2] Oct. 27 PM

演示文件

提示:该报告下的文件权限为仅限参会人,您尚未登录,暂时无法查看。

摘要
Bi₂O₃ thin films prepared by sol-gel processing are attractive for electrochromic energy-storage electrodes because the same reversible charge-insertion reaction can generate visible color change and capacitive response. In this work, Bi₂O₃ films with thicknesses of approximately 70, 100, 130, and 160 nm were deposited on FTO glass by repeated spin coating of a citrate-assisted Bi precursor sol, followed by annealing in air at 400°C. The thickness series was used to clarify how active material loading and transport accessibility jointly control the white-to-black-brown electrochromic response. XRD confirmed crystalline Bi₂O₃, while SEM/EDS and XPS indicated thickness-dependent morphology, Bi-O bonding, and surface oxygen-containing species. Among the investigated films, the 130 nm sample gave the strongest redox response, the largest optical modulation at 633 nm (63.5%), bleaching/coloring times of 39.8/40.4 s, and a coloration efficiency of 9.3 cm²·C⁻¹. It also showed the most favorable areal-capacitance trend and transmittance changes synchronized with galvanostatic charge/discharge. Figure 1 summarizes the key electrochromic and charge-storage behavior of the optimized film. The results suggest that the optimized thickness balances film continuity, surface accessibility, and ion/electron transport in sol-gel-derived Bi₂O₃ electrodes.
 
关键词
Sol-gel; Thin film; Electrochromism; Energy storage; Surface chemistry
报告人
Denghu Yu
Xiamen University of Technology

稿件作者
登湖 余 厦门理工学院
东亚 孙 厦门理工学院
发表评论
验证码 看不清楚,更换一张
全部评论
重要日期
  • 会议日期

    10月26日

    2026

    至

    10月30日

    2026

  • 10月17日 2026

    初稿截稿日期

  • 10月30日 2026

    注册截止日期

主办单位
杭州市北京航空航天大学国际创新研究院(北京航空航天大学国际创新学院)
联系方式
历届会议
移动端
在手机上打开
小程序
打开微信小程序
客服
扫码或点此咨询