SinoGreenTech Academic Portal
CY
Verified CAS / Academic Author2 Decoded Studies

Prof. Chi Yu

School of Materials Science and Engineering, Nanchang Hangkong University

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3887-6

Impedance-Matchable 3D MXene Sponge/NiFe@NC Heterostructure with Tunable Pores for Efficient Electromagnetic Wave Absorption and Thermal Resistance

The proliferation of 5G/6G communications and radar systems has intensified electromagnetic wave (EMW) leakage, interference, and thermal management challenges. This study presents a 3D MXene sponge/NiFe@NC heterostructure with tunable pore architecture, fabricated by pyrolyzing a polyurethane (PU) foam template uniformly coated with NiFe-decorated Ti3C2Tx MXene nanosheets. The resulting porous dielectric-magnetic network integrates interconnected MXene pathways with uniformly dispersed NiFe@NC nanoparticles, enabling synergistic dielectric-magnetic loss via conduction loss, dipole/interface polarization, and magnetic loss. Precise pore structure design enhances impedance matching and promotes multi-scattering and internal reflection of EMWs. An 'EMW-pore matching' mechanism is proposed, where pore size governs impedance matching at specific frequencies, enabling tunable absorption performance. The optimized absorber achieves a reflection loss (RL) of -67.84 dB, while radar cross-section (RCS) simulations confirm exceptional attenuation and stealth potential. Additionally, the 3D skeleton derived from PU foam confers remarkable thermal resistance and flame retardancy. This pore-regulation strategy provides a scalable route to designing lightweight, broadband, and thermally stable EMW absorbers for next-generation communication and stealth applications.

New Carbon Materials2026DOI: 10.1016/S1872-5805(26)61106-7

Stabilization of Sulfur Species in Coal-Derived Hard Carbon via Micropore Confinement and Chemical Bonding for Enhanced Sodium Storage

Hard carbon anodes for sodium-ion batteries suffer from limited capacity, low initial Coulombic efficiency, and poor long-term cycling stability. To address these issues, we report a dual-stabilization strategy that combines micropore confinement and chemical bonding to control sulfur species in coal-derived hard carbon. Bituminous coal, with its naturally condensed aromatic framework, serves as the carbon precursor. A two-step thermal process first constructs a microporous carbon framework, followed by gas-phase sulfidation to introduce sulfur. The sulfur is confined within micropores and forms stable covalent C–S bonds with the carbon matrix, providing synergistic physical–chemical stabilization. This suppresses sulfur migration, prevents interfacial side reactions, and introduces additional redox-active sites. The optimized sample (HC-10) delivers a high reversible capacity of 450 mAh/g after 800 cycles at a current density of 1 A/g, with excellent rate capability and cycling stability. Mechanistic analysis reveals that the stabilized sulfur species reversibly participate in sodium-ion storage and improve interfacial kinetics. This work provides an effective strategy for stabilizing sulfur in coal-derived carbon materials and offers insights into the design of high-performance anodes for sodium-ion batteries.