The electrochromic/capacitive dual-functional materials based on the synergistic effect between LixNiOy nanosheet arrays and aqueous Zn2+/K+ composite electrolyte ions
ID:38 Submission ID:56 View Protection:ATTENDEE Updated Time:2026-10-21 09:18:49 Hits:9 Oral Presentation

Start Time:2026-10-29 16:40 (Asia/Shanghai)

Duration:10min

Session:[D4] Thursday 29 October 2026 » [S6] Oct. 29 PM

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Abstract
NiO Nickel oxide (NiO) normally functions in alkaline electrolyte, which conflicts with WO3’s acidic or organic operating environments. Most WO3-NiO complementary devices use Li+-containing organic solutions as the electrolytes, which lead to low NiO electrochromic activity and safety hazards. Herein, Li-doped NiO (LixNiOy) nanosheet arrays were hydrothermally grown on FTO glass, and their electrochromic and pseudocapacitive behaviors were investigated in Zn2+/K+ aqueous electrolyte (Figures a–c.). LixNiOy delivers optical modulations of 39.01% at 600 nm and 21.62% at 1200 nm, outperforming pure NiO. It reversibly switches between colouring and bleaching states, with preferential visible-light absorption and partial near-infrared transmittance, offering spectral complementarity to WO3. After 500 coloration/bleaching cycles, LixNiOy retains 68.39% optical modulation, far exceeding the 33.82% retention of pure NiO. The material exhibits areal specific capacitance of 5.16 mF/cm2 at 0.01 mA/cm2. In addition, the material showed a high coulombic efficiency (>95%) and good stability (62.0% capacitance retention after 1000 cycles) (Figures d–i.). Despite inferior optical modulation compared with alkaline/organic systems originating from the large hydrated radius and strong electrostatic interaction of Zn2+, the warm-mode spectral regulation and WO3-compatible characteristics enable a promising strategy for all-aqueous, low-cost, safe dual-band smart windows.
 
Keywords
Li-doped NiO;electrochromism;aqueous electrolyte;WO3;nanosheet arrays;dual-band smart window;pseudocapacitance
Speaker
Zhongyi Wang
University of Science and Technology Beijing

Submission Author
Zhongyi Wang University of Science and Technology Beijing
Xiangtao Huo University of Science and Technology Beijing
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