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Verified CAS / Academic Author2 Decoded Studies

Prof. ZHOU Yuxuan

Shanghai Institute of Ceramics, Chinese Academy of Sciences

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-4107-x

Quaternary Ammonium-Mediated I+ Complexation for Stable High-Energy Four-Electron Aqueous Fiber Zinc-Iodine Batteries

Aqueous fiber zinc-iodine batteries (FZIBs) with four-electron redox exhibit inherent safety and high energy density for wearable electronics. Nevertheless, their practical implementations are hindered by unsatisfactory cycling stability and low realistic energy density, mainly caused by severe H2O-induced nucleophilic attack toward iodine species and poor zinc anode reversibility. Here, we report a quaternary ammonium-mediated coordination strategy to simultaneously address the irreversible cathode/anode redox behavior and thus promote the electrochemical performance of four-electron FZIBs. The cationic choline ion (Ch+) induces complexation with ICl2− via electrostatic interaction, homogenizing the electron cloud density and suppressing irreversible hydrolysis of I+ species, enabling a reversible near-theoretical high capacity of 418.3 mAh g−1. Meanwhile, preferentially adsorbed Ch+ on the zinc anode surface creates positively charged shielding layers, mitigating the tip effect caused by localized electric field and achieving robust zinc stripping/plating. The enhanced cathode/anode reversibility and improved interfacial stability enable stable FZIBs operation for over 20,000 cycles at 20.0 A g−1. Moreover, successful integration of FZIBs into electronic textiles with glucose and cardiac rhythm sensors demonstrates great potential for next-generation wearable electronics.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3395-4

Near-Room-Temperature Ferromagnetic 1T Nb1−xCrxTe2 from Doping-Induced Phase Transition of 1T′ NbTe2

Magnetic transition metal dichalcogenides (TMDs) offer intrinsic spin polarization for spintronic devices, yet ferromagnetic TMDs remain scarce. The theoretically predicted nontrivial topological 1T NbTe2 is thermodynamically unstable relative to the 1T′ phase under ambient conditions, impeding its spintronic application. Heteroatom doping can stabilize the 1T phase and introduce magnetism. We synthesized Nb1−xCrxTe2 (x = 0, 0.1, 0.2, 1/3, 0.4) crystals and discovered the 1T Nb2/3Cr1/3Te2 phase. Cr doping induces a 1T′-to-1T structural transition in NbTe2. Density functional theory confirms the thermodynamic stability of 1T Nb2/3Cr1/3Te2. Magnetic measurements reveal a transition from diamagnetic to ferromagnetic behavior with increasing Cr content. The ferromagnetism in 1T Nb2/3Cr1/3Te2 originates primarily from localized Cr 3d electrons, achieving a Curie temperature (TC) of 254 K, surpassing most Cr-based van der Waals ferromagnets. The compound exhibits metallic behavior coexisting with the Kondo effect and a positive magnetoresistance of 32.1% at 2 K under μ0H = 9 T. This work unveils a doping-induced phase transition mechanism and provides a new layered ferromagnetic material for spintronic devices.