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In this study, a Cu 2 O–Au nanoparticles (NPs) heterojunction catalyst anchored on wood was developed by in situ reduction and hydrothermal treatment, and the properties of the catalyst were systematically characterized. The catalyst exhibited prominent photocatalysis of methyl orange (MO, 0.169 min− 1), and tetracycline (TC, 0.122 min−1) which were degraded completely within 20 min. Even after four recyclings, the efficiency of MO degradation by the catalyst remained at 80%. The natural wood with three-dimensional porous structures acted as a reducing agent and a stabilizer for Au NPs and Cu 2 O, which helped to maintain high performance and reusability. The presence of Au NPs mediated the light-induced electron transfer and enhanced the absorption of visible light for promoting photocatalytic activity. The intermediates of contaminants within the degradation process were characterized by liquid chromatography-mass spectrometry. Additionally, the photogenerated superoxide radicals and holes were identified by electron spin resonance. Thus, the potential degradation mechanism catalyzed by the Cu 2 O–Au NPs-wood was proposed. This findings of this study valorizes biomass as a photocatalyst for wastewater remediation. Preparation of a heterogeneous Cu 2 O–Au NPs-wood photocatalyst and its application. [Display omitted] • Cu 2 O–Au NPs-wood heterojunction exhibits highly catalytic property. • Conductive porous carbonized wood enhances the photocatalytic performance. • Cu 2 O–Au NPs-wood can effectively photocatalytic degrade MO and TC. • The degradation of pollutant photo-catalyzed by heterojunction is elucidated. [ABSTRACT FROM AUTHOR]

Abstract: By using a surface-modified templating method, Fe2O3@polypyrrole (PPy) core/shell spindles have been successfully prepared in this paper. The Fe2O3 particles with spindle morphology were initially fabricated as core materials. After the PVP modification, the Fe2O3 spindles were subsequently coated with a tunable thickness layer of PPy by in situ deposition of the conducting polymer from aqueous solution. Hollow PPy spindles were produced by dissolution of the Fe2O3 core from the core/shell particles. High-temperature treatment under vacuum condition covert the hollow PPy spindles into carbon capsules by carbonization of the PPy shell. Transmission electron microscope (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS) confirmed the formation of the Fe2O3@PPy core/shell particles, PPy and carbon capsules with spindle morphology. [Copyright &y& Elsevier]