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Verified CAS / Academic Author2 Decoded Studies

Prof. LI Chunzhong

East China University of Science and Technology

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3714-3

Topological Chitosan Framework Enables Reversible Columnar Array Anodes for High-Performance Aqueous Zinc Batteries

Eco-friendly aqueous zinc batteries (AZBs) are promising alternatives to lead-acid batteries in applications requiring both safety and energy density. However, their practical deployment is hindered by the synergistic deterioration of zinc anodes—structural collapse and kinetic failure—under high depth of discharge (DOD) and high current densities, which severely limits actual energy and power densities. Here, we report a strategy for the in situ integration of a double-layer topological chitosan framework (D-CTS) on current collectors via regulating phase separation kinetics during multistage coordination-neutralization electrophoresis. The vertical through-hole array is formed by coupling instantaneous and delayed phase separation. Subsequently, a columnar zinc array is mediated by D-CTS to construct an integrated component (D-CTS-Zn) comprising a vertical through-hole separator and an array anode. The embedded interconnected nanonetworks within the through-hole walls enable dynamic equilibrium of the columnar zinc array through a lateral ion compensation mechanism. As a result, Zn||Zn symmetric cells with D-CTS-Zn stably cycle over 3000 cycles at 200 mA cm−2 under 60% DOD. The assembled D-CTS-Zn||MnO2 battery delivers an energy density of 83 Wh kg−1 at an ultrahigh power density of 9.25 kW kg−1. This work provides a constructive strategy for chitosan phase separation regulation and separator-induced reversible metal array anodes.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3411-3

Ag/Pt co-modified FeCoNiOx spinel oxides enhancing interface water dissociation to boost selective ethanol electrooxidation to acetate

Electrochemical valorization of ethanol to acetate offers a low-potential alternative to oxygen evolution, but industrial adoption is constrained by insufficient current density and catalyst durability. This work reports FeCoNiOx spinel oxides co-modified with Pt and Ag (FeCoNiOx-PtAg) that enhance interfacial water dissociation to generate moderate *OH coverage while suppressing *OH over-oxidation to *O. The catalyst achieves a maximum Faradaic efficiency (FE) of 98.1% for acetate at 100 mA cm−2, a peak partial current density of 291.2 mA cm−2, and stability exceeding 100 h. In-situ attenuated total reflection surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) reveals that Pt and Ag co-modification regulates water dissociation, maintaining *OH at levels optimal for nucleophilic attack on CH3CO* intermediates. Techno-economic analysis confirms that the paired ethanol oxidation and hydrogen evolution system is cost-effective and low-carbon. The results establish a viable pathway for selective ethanol electrooxidation to acetate at industrially relevant current densities.