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Verified CAS / Academic Author2 Decoded Studies

Prof. Mingshan Han

Not explicitly stated in the provided text; likely a Chinese university or research institute.

Research Publications & English Decoded Briefs

Showing 2 publications
Environmental Chemistry2026DOI: 10.7524/j.issn.0254-6108.2026012804

Characteristics and Source Apportionment of Volatile Organic Compounds at a Roadside Site in a Tropical City during Summer

This study conducted online monitoring of volatile organic compounds (VOCs) at a roadside site on a main arterial road in Haikou, a tropical city, during summer 2023 (June 25–September 30). A total of 56 VOCs were measured. The mean total VOC concentration (φ(TVOCs)) was (9.05 ± 6.24) nmol·mol−1, with concentrations in the order: alkanes > alkenes > aromatic hydrocarbons > alkynes, dominated by light alkanes. Alkenes and aromatic hydrocarbons contributed significantly to atmospheric chemical reactivity, while secondary organic aerosol formation potential (SOAFP) was limited, influenced by both VOC concentrations and temperature. VOC concentrations exhibited a pronounced bimodal diurnal pattern, consistent with traffic peaks. Ratio analysis indicated a Toluene/Benzene (T/B) ratio slightly higher than typical vehicle exhaust values, and an iso-Pentane/n-Pentane (i/n) ratio suggesting fuel evaporation influence. Positive Matrix Factorization (PMF) identified four sources: gasoline/LPG vehicle exhaust (49.9%), solvent use or vehicle evaporation (26.1%), diesel vehicle exhaust (14.9%), and biogenic sources (9.1%). SOAFP was mainly contributed by solvent use/evaporation (35.7%), gasoline/LPG exhaust (34.6%), diesel exhaust (22.0%), and biogenic sources (7.7%). These findings indicate that under tropical summer high-temperature conditions, roadside VOC pollution is predominantly traffic-related, with vehicle evaporation sources non-negligible, providing insights for evaluating vehicular impacts on particulate pollution.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4123-0

Entropy-Driven Modulation Enables Atomic-Level Interactions for High-Rate Capacity Cathode Materials in Rechargeable Aqueous Aluminum-Ion Batteries

Aqueous aluminum-ion batteries (AAIBs) are promising for large-scale energy storage due to safety, sustainability, and theoretical high capacity. However, sluggish electron/ion transport in conventional cathodes limits rate capability. Here, we first propose high-entropy engineering of metal oxides (HEOs) as cathodes in AAIBs, leveraging the 'cocktail effect' and abundant electron transport pathways to enhance rate-capacity. Atomic-level interactions between different metal atoms broaden the d-band with reduced electronic level degeneracy, facilitating rapid electron transport, achieving one of the best rate capabilities (119.4 mAh g−1 at 10.0 A g−1) among metal-oxide cathodes. The disordered layered oxides formed with a high-entropy framework alleviate electrostatic repulsion between aluminum ions and the fixed lattice, mitigating structural degradation and imparting excellent cycling stability (over 95.1 mAh g−1 after 500 cycles at 2.0 A g−1). The optimized HEO-Cr cathode (Fe0.6Co0.6Ni0.6Mn0.6Cr0.6O4) exhibits outstanding rate performance and cycling stability. DFT simulations and electrochemical tests reveal that multi-transition metal incorporation, bandgap narrowing, and unique lattice structure drastically enhance electron transport efficiency. The layered phase formed after cycling, based on a high-entropy framework, overcomes challenges from high charge density aluminum ions, significantly enhancing cycling stability. This work paves the way for high-performance AAIBs and other aqueous multivalent metal ion batteries by rationally designing high-entropy engineering.