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Updated: Jan 7, 2026

Protocol of Electrochemical Test and Characterization of Aprotic Li-O2 Battery
Published on: July 12, 2016
Hydro-photo-synergy unlocks deep and reversible chemistry of solid-state lithium-oxygen batteries
Sijia Chi1,2,3, Zhenshen Li1,2,3, Xunjie Yin1,2,3
1Nanoyang Group, Tianjin Key Laboratory of Advanced Carbon and Electrochemical Energy Storage, School of Chemical Engineering and Technology, National Industry-Education Integration Platform of Energy Storage, and Collaborative Innovation Centre of Chemical Science and Engineering, Tianjin University Tianjin 300072 China wushichao@tju.edu.cn qhyangcn@tju.edu.cn.
Abstract:
Harnessing light to drive high-energy batteries is an intriguing goal, yet photoactivity often fails for reasons that have remained elusive, which is starkly exemplified in photo-assisted solid-state lithium-oxygen batteries. Here, we identify photo-shielding by opaque, ionically resistive discharge products as the critical, previously overlooked failure mechanism. This "catalyst blinding" effect not only blocks light but also passivates the electrochemical interface, causing a catastrophic kinetic shutdown. We overcome this limitation with a "hydro-photo-synergy" strategy, using controlled water vapor to shift the solid-state electrochemistry from a 2e- to an efficient 4e- pathway and transform the product into highly transparent, ionically conductive products. This dual optical and electrochemical enhancement sustains photocatalysis for deep and reversible reactions, unlocking a 2-fold increase in accessible capacity, a low overpotential (0.3 V), and outstanding stability (>170 cycles for 34 mA h cm-2). This work establishes in situ product engineering as a new paradigm to unlock high-energy solid-state photo-electrochemical devices.
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