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Prof. LI Yuhang

East China University of Science and Technology

Research Publications & English Decoded Briefs

Showing 3 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4404-7

Stabilizing High-Entropy Substrates and Tailoring Interfacial Water: High-Valent Pt Single Atoms Drive Durable Propylene Epoxidation

Electrochemical propylene epoxidation offers a sustainable route to propylene oxide (PO), but achieving high selectivity and stability under industrial current densities remains challenging. Herein, we report a high entropy amorphous CoFeNiCrMnBOx borate loaded with high valence Pt single atoms catalyst (a-Pt-HEBO) for stable bromine radical-mediated propylene epoxidation reaction (BrPOR). The high-entropy amorphous structure reshapes the interfacial hydrogen-bonding network and enriches free water, substantially lowering the energy barrier for water dissociation. Meanwhile, the strong electronic interactions between the coordinatively unsaturated, high-valence single Pt atoms and the substrate effectively prevent transition metal dissolution at high anodic potentials. The catalyst achieved 82.1% Faraday efficiency of PO at an industrial grade current density of 100 mA cm-2, and demonstrated excellent industrial application stability in up to 500 h of continuous test and within a scaled-up electrolyzer (4 × 4 cm2). This work provides a design for high-entropy catalysts in halogen-mediated electrosynthesis and a viable pathway toward carbon-neutral PO production.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4164-3

Dual-Layered Organo-Fluorinated Hetero-Interphase: A Robust Shield for Ultra-Stable Lithium Metal Batteries

Lithium metal anodes (LMAs) are pivotal for next-generation high-energy batteries, yet their commercialization is hindered by dendrite growth and unstable solid electrolyte interphase (SEI). Here, we report a dual-layered artificial SEI (ASEI) comprising an inner LiF-rich inorganic layer and an outer perfluoropolyether (PFOE) organic layer, fabricated via a scalable roll-pressing technique. The LiF-rich layer lowers Li-ion diffusion barriers and provides mechanical robustness, while the PFOE layer chemically stabilizes the interface against electrolyte oxidation. Symmetric cells with PFOE-LiF@Li anodes achieve over 1400 h of stable cycling at 30 mA cm−2 and 5 mAh cm−2. Full cells paired with LiFePO4 cathodes deliver 350 cycles at 1 C and over 550 cycles at 2 C with high capacity retention and Coulombic efficiency. This work establishes a design principle for interfacial engineering, combining inorganic rigidity with organic functionality, and offers a promising route for practical LMBs.

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.

Prof. LI Yuhang | Publications & Academic Profile | SinoGreenTech | SinoGreenTech