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Verified CAS / Academic Author2 Decoded Studies

Prof. Haitao Li

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences

Research Publications & English Decoded Briefs

Showing 2 publications
Environmental Chemistry2026DOI: 10.7524/j.issn.0254-6108.2024042404

CaO-Doped Rh/Al2O3 as a Highly Effective Catalyst for Catalytic N2O Decomposition

The direct catalytic decomposition of the greenhouse gas N2O into nitrogen and oxygen holds significant environmental importance. In this study, CaO-modified Rh-based catalysts were prepared via a stepwise impregnation method. The catalyst structures were characterized, and their catalytic performances for N2O decomposition were investigated. The characterization results demonstrate that CaO doping significantly enhances catalytic activity and water resistance. Specifically, the 0.5Rh/Al2O3 catalyst exhibited a N2O conversion below 5% at 300 °C, whereas the 0.5Rh-4Ca/Al2O3 catalyst achieved 50% conversion under identical conditions, indicating markedly improved low-temperature activity. Compared to the undoped catalyst (0.5Rh/Al2O3), CaO doping (0.5Rh-xCa/Al2O3) strengthens metal-support interactions, improves Rh dispersion on the support surface, and modulates the electron density around Rh, thereby substantially boosting N2O decomposition capability. The catalyst also demonstrated excellent stability, maintaining essentially constant conversion over 40 h of reaction. These findings underscore the potential of alkaline earth metal oxide doping as an effective strategy for designing high-performance noble metal catalysts for N2O abatement.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3917-x

Intercalation-Engineered MOF for Ultrasensitive Ratiometric Fluorescent Sensing of Enoxacin

The escalating global challenge of antibiotic contamination demands advanced sensing technologies for environmental monitoring and public health protection. Here, we present a structurally well-defined, intercalation-engineered metal-organic framework (MOF), HSB-W18, which functions as an ultrasensitive and selective fluorescence sensor for fluoroquinolone antibiotics. Single-crystal X-ray diffraction analysis unambiguously determined both the framework architecture and the spatial organization of intercalated 2,5-dihydroxyterephthalate molecules at atomic resolution. Through ultrasound-assisted synthesis, highly stable book-shaped microsheets (HSB-W18-MS) were obtained, maintaining exceptional aqueous dispersibility and luminescence intensity for over one month. These microsheets offer distinct advantages for antibiotic detection: specific recognition of diverse fluoroquinolones via unique fluorescence signatures; highly sensitive ratiometric detection of enoxacin (ENX) with a limit of detection (LOD) of 5.62 nM and rapid response kinetics (<30 s); exceptional selectivity alongside reusability. Systematic mechanistic investigations revealed a synergistic detection process involving multiple photophysical pathways. Furthermore, a smartphone-based portable detection system was successfully implemented, and the practical utility of the sensor was validated by quantifying ENX in complex environmental samples: tap water LOD = 18.32 nM and river water LOD = 29.87 nM. This study contributes to fundamental materials science and environmental monitoring by elucidating discernible structure-property relationships in intercalated MOFs, demonstrating a robust platform for field-deployable antibiotic detection and proposing an innovative design paradigm for environmental optical sensors.