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Capacitance Enhancement in a Semiconductor Nanostructure-Based Supercapacitor by Solar Light and a Self-Powered Supercapacitor–Photodetector System

  • Minshen Zhu
  • , Yang Huang
  • , Yan Huang
  • , Zengxia Pei
  • , Qi Xue
  • , Hongfei Li
  • , Huiyuan Geng
  • , Chunyi Zhi*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

The effects of the environment on the energy storage of supercapacitors as well as the underlying mechanisms have long been neglected. This paper reports that the capacitance of hexagonal-phase tungsten oxide (h-WO3)-based supercapacitors increases by ≈17% under solar light. Thorough analyses of the wavelength dependence of the enhancement, capacitive mechanism, energy storage dynamics, and impedance reveal that: i) photoexcited electrons are responsible for the enhancement; ii) the insertion of protons into the large hexagonal tunnels of h-WO3, instead of a surface capacitive process, is greatly facilitated by the photoexcited electrons; iii) the theoretical light-induced capacitance enhancement can reach up to 38% for a h-WO3-based supercapacitor. Moreover, as an application of this finding, a self-powered photodetector based on a h-WO3 supercapacitor is fabricated, wherein the photoexcited electrons serve as the signal for detecting solar light. The device works without an external power source and can be considered as an ultimately integrated power source–sensor system. This work sheds light on the interaction between solar light and a semiconductor-based supercapacitor as well as the concrete mechanisms behind the phenomenon. These efforts also open the door to the design of highly integrated, brand-new power source–sensor systems.

Original languageEnglish
Pages (from-to)4481-4490
Number of pages10
JournalAdvanced Functional Materials
Volume26
Issue number25
DOIs
StatePublished - 5 Jul 2016

Keywords

  • multifunctional energy storage device
  • photodetector
  • photoexcited electron
  • supercapacitor
  • tungsten oxide

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