Published December 2021 | Version v1
Journal article

Designing a hybrid type photoelectrochromic device with dual coloring modes for realizing ultrafast response/high optical contrast self-powered smart windows

  • 1. Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 10607 (China)
  • 2. Department of Chemical Engineering, National Taiwan University, Taipei 10617 (China)
  • 3. Institute of Polymer Science and Engineering, National Taiwan University, Taipei 10617 (China)
  • 4. Advanced Research Center for Green Materials Science and Technology, National Taiwan University, Taipei 10617 (China)

Description

Highlights: • A brand new design of a hybrid type photoelectrochromic device (H-PECD) was proposed for the first time. • Independently covered photoelectrode solved the bottleneck of electrochromic material selection. • A bifunctional counter electrode possesses optical complementary and electrocatalytic ability. • Duel-coloring modes of high optical contrast and ultrafast response for H-PECD can be achieved. • H-PECD provided a new strategy to realize the self-powered smart windows for green building. The self-powered smart window is a promising wire-free system to integrate on the energy-saving building due to its independent and sustainable operations without an external power source. Solar-driven photoelectrochromic devices (PECDs), which derived from the hybridization of dye-sensitized solar cells (DSSCs) and electrochromic devices (ECDs), are potential systems to realize the convenient self-powered smart window. To further boosting up the optical contrast and minimizing the response time, in this study, a brand new hybrid type photoelectrochromic device (H-PECD) composed with a new architecture of independently covered photoelectrode with electrochromic conducting polymeric layer and a novel counter electrode (CE) with bifunctional electrochemical layer is proposed in the first time. Compared to traditional combined-type PECDs (C-PECD), the electrochromic and the photoactive layers are independently integrated on the photoelectrode to overcome the limitation of electrochromic material selection. By taking this advantage, a conducting polymer of PEDOT-MeOH with high coloration efficiency can be introduced to serve as the electrochromic layer for further enhancing the optical performance of H-PECD. Furthermore, a highly transparent electrochemical layer serves as bifunctional CE for not only facilitating the I3- reduction reaction for accelerating the bleaching rate, but also contributes additional optical contrast of 3% under coloring process. By comparing with another classic configuration of separated type PECD (S-PECD), the coloring and bleaching time of H-PECD can be shortened within 5 s under maximum transmittance change at 600 nm for 31.7% since the photovoltaic performance and photo-coloration efficiency (PhCE) is improved by integrating with bifunctional CE. By taking advantage of H-PECD, duel-coloring modes of high optical contrast and ultrafast response can be achieved by controlling the operating processes. This research is a substantial advancement toward the practical application of PECDs and self-powered smart windows.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.nanoen.2021.106575

Additional details

Identifiers

DOI
10.1016/j.nanoen.2021.106575;
PII
S2211285521008272;

Publishing Information

Journal Title
Nano Energy (Print)
Journal Volume
90
Journal Page Range
vp.
ISSN
2211-2855

INIS

Country of Publication
Netherlands
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
54014579
Subject category
S36: MATERIALS SCIENCE; S14: SOLAR ENERGY;
Descriptors DEI
DESIGN; ELECTROCHEMISTRY; ELECTROCHROMISM; ELECTRODES; LAYERS; PERFORMANCE; PHOTOVOLTAIC EFFECT; POLYMERS; SOLAR CELLS
Descriptors DEC
CHEMISTRY; DIRECT ENERGY CONVERTERS; ELECTRO-OPTICAL EFFECTS; EQUIPMENT; PHOTOELECTRIC CELLS; PHOTOELECTRIC EFFECT; PHOTOVOLTAIC CELLS; SOLAR EQUIPMENT

Optional Information

Copyright
Copyright (c) 2021 Elsevier Ltd. All rights reserved.