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Prof. CHENG Hui-Ming

Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3352-6

2D Gate-All-Around Logic Devices: A Path Toward Monolithic 3D Circuits Beyond Silicon

The relentless scaling of silicon transistors below 5 nm gate lengths has exposed fundamental limits: dangling-bond-induced interface scattering exacerbates short-channel effects, including direct source-drain tunneling and drain-induced barrier lowering, degrading power consumption, signal integrity, and reliability. Gate-all-around field-effect transistors (GAAFETs) mitigate these effects by fully enclosing the channel, but silicon's surface chemistry remains problematic. Two-dimensional (2D) semiconductors offer dangling-bond-free surfaces, atomic-level thickness uniformity, and high electron mobility, enabling sub-1-nm gate lengths without short-channel effects. Their van der Waals layered structure further permits monolithic 3D (M3D) integration for high-density, low-power circuits. Despite theoretical promise, 2D GAA devices face critical bottlenecks in source-drain contacts, gate dielectrics, and interface engineering. The deposition of high-quality, atomically uniform, low-trap-density high-k dielectrics on 2D surfaces is particularly challenging. Tang et al. addressed this by forming layered oxide Bi2SeO5 (k = 21) on Bi2O2Se via ultraviolet-assisted intercalative oxidation, creating an atomically smooth, lattice-matched van der Waals interface. The resulting fully encapsulated 2D Bi2O2Se/Bi2SeO5 GAA heterostructure enabled GAAFETs with equivalent oxide thickness below 0.5 nm, subthreshold swing of ~62 mV dec-1 over five orders of magnitude, electron mobility exceeding 280 cm2 V-1 s-1, and stable operation at 0.5 V with on-current exceeding 1 mA μm-1. These metrics demonstrate superior electrostatic control compared to silicon and other 2D GAAFETs, providing a viable route to M3D circuits beyond silicon.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3499-6

Facile synthesis of sp2-enriched hard carbon anodes for high-efficiency sodium storage

Biomass-derived hard carbons (HCs) are promising anodes for sodium-ion batteries (SIBs) due to their low cost, renewable nature, and structural stability, yet their practical application is hindered by a low initial Coulombic efficiency (ICE) and inadequate rate capability. Herein, we report a tri-functional nitric acid treatment coupled with one-step carbonization to synthesize a hard carbon with a sp2-C-dominated structure. The process not only eliminates impurities but also selectively dissolves lignin in the biomass, thereby promoting the alignment of graphite microcrystals. At the same time, edge-N and C=O groups are grafted onto the carbon skeleton, which together produce an HC with an optimized interlayer spacing and abundant closed micropores. These structure modifications collectively increase Na+ adsorption kinetics in the sloping region and enable efficient sodium storage in the low-voltage plateau region, yielding a high ICE of 91.69% and a remarkable rate capability, with 83.9% capacity retention at 600 mA g−1. A full SIB cell using this HC anode with a Na3V2(PO4)3 cathode delivers an energy density of 213.14 Wh kg−1, demonstrating its practical potential. This work offers a simple and scalable engineering strategy to overcome the performance vs. manufacturing cost dilemma in developing HC anodes.