Demonstrates enhanced interfacial stability in electrochromic devices, indicating improved performance.
Aqueous Zn‐WO 3 electrochromic devices (ZWEDs) represent a promising frontier in energy‐efficient electrochromic systems. However, their practical application is hindered by the short device lifespans due to the poor electrode/electrolyte interfacial stability which originates from high water activity. Herein, we develop a eutectic‐polymer dual‐network electrolyte to regulate water activity and stabilize the electrode/electrolyte interface. Combined in situ/ex situ spectroscopic analysis and simulations reveal that this eutectic‐polymer dual‐network stabilize the electrode structure via two complementary effects: (i) reconstruction of the hydrogen‐bond network confines free water molecules, suppressing water activity and parasitic reactions; and (ii) preferential adsorption of acetamide molecules over water on the electrode surfaces forms a stable molecular interfacial layer that regulates Zn 2+ electrochemical behavior and further mitigates water‐induced side reactions. Benefiting from the synergy between hydrogen‐bond reconstruction and interfacial adsorption, the interfacial stabilities of both Zn anode and WO 3 cathode are significantly enhanced. Consequently, the Zn‐WO 3 device achieves outstanding cyclic stability in both ion storage and optical modulation over 1000 cycles, with an operational temperature range expanded to −30°C∼80°C. This strategy offers a promising pathway to enhance the interfacial stability in ZWEDs across a wide temperature range.
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Wan et al. (2026) studied this question.
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