Interfacial Engineering of Zn Metal via a Localized Conjugated Layer for Highly Reversible Aqueous Zinc Ion Battery

Abstract

Aqueous zinc‐ion batteries are regarded as promising and efficient energy storage systems owing to remarkable safety and satisfactory capacity. Nevertheless, the instability of zinc metal anodes, characterized by issues such as dendrite growth and parasitic side reactions, poses a significant barrier to widespread applications. Herein, we address this challenge by designing a localized conjugated structure comprising a cyclic polyacrylonitrile polymer (CPANZ), induced by a Zn2+‐based Lewis acid (zinc trifluoromethylsulfonate) at a temperature of 120 °C. The CPANZ layer on the Zn anode, enriched with appropriate pyridine nitrogen‐rich groups (conjugated cyclic −C=N−), exhibits a notable affinity for Zn2+ with ample deposition sites. This zincophilic skeleton not only serves as a protective layer to guide the deposition of Zn2+ but also functions as proton channel blocker, regulating the proton flux to mitigate the hydrogen evolution. Additionally, the strong adhesion strength of the CPANZ layer guarantees its sustained protection to the Zn metal during long‐term cycling. As a result, the modified zinc electrode demonstrates long cycle life and high durability in both half‐cell and pouch cells. These findings present a feasible approach to designing high performance aqueous anodes by introducing a localized conjugated layer.

Intrinsic mechanism of Co/Mn elemental manipulation in enhancing the cycling stability of single-crystal ultrahigh-nickel layered cathodes

“…Among them, the high-nickel layered oxides (LiNi x Co y Mn z O 2 and LiNi x Co y Al z O 2 , referred to as NCM and NCA, with x ≥ 0.8) are considered highly promising cathodes owing to their high energy density and cost-effectiveness with the reduced Co content. 2–5…”