Browsing by Author "Qin, C"

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    Boosting CO2-to-C2H4 electrocatalysis on Cu2O with waste-derived porous carbon from coconut shells
    (Royal Society of Chemistry, 2026) Qin, C; Li, T; Masakorala, G; Zhi, C; Huang, H; Zhou, C; Wang, X; Shen, B; Zhang, Jian-Rong; Zhou, Y
    This study presents a sustainable strategy to boost CO2-to-C2H4 conversion by constructing Cu–C interfaces using Cu2O nanospheres supported on porous carbon derived from waste coconut shells. The Cu2O–10mgC catalyst achieves a 4-fold increase in FE(C2H4) compared with Cu2O and maintains >40% selectivity for 45 h. In situ spectra reveal enhanced *COLFB coverage, confirming that oxygen-rich functional groups at the Cu–C interface promote C–C coupling. This work demonstrates both the catalytic and economic feasibility of waste-derived carbon supports for efficient CO2-to-C2H4 conversion.
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    PublicationOpen Access
    Coconut Shell Waste-Derived Porous Carbon-Supported Sn Catalysts for Efficient Electrochemical CO2Reduction to Formic Acid and Deuterated Formic Acid
    (American Chemical Society, 2025-11-05) Qin, C; Masakorala, G; Mohideen, M; Samarasekara, T; Zhang, L; Zhu, W; Zhou, Y; Thambiliyagodage, C
    Industrial-level electrochemical CO2 reduction reaction (CO2RR) to form HCOO– and DCOO– requires robust Sn catalysts with high performance. In this study, the hydrothermal method was employed to load varying amounts of Sn precursors onto waste biomass-derived porous carbon to investigate the structure–activity relationship between Sn loading forms and HCOO– selectivity. Through comprehensive ex/in situ characterizations, we discovered that with 5% Sn precursor addition, highly dispersed SnO2 nanoparticles formed on the carbon support, enabling the catalyst to exhibit exceptional HCOO– activity (Faradaic efficiency exceeding 90%) across a broad potential window. In situ attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) and in situ Raman spectroscopy revealed that the highly dispersed SnO2 nanoparticles enhance the stability of the *OCHO intermediate. Furthermore, when H2O was replaced with D2O, the generation of DCOO– was observed, and good selectivity was maintained. This study provides a facile strategy for waste biomass conversion and the design of Sn-based catalysts for DCOO– production.