Construction of a floatable copper/corncob biochar composite with an LSPR effect for CO2 capture and efficient photothermal catalytic conversion

Abstract

The synthesis of high-value chemicals through the photothermal reduction of carbon dioxide is of great significance for addressing energy shortages and environmental challenges; however, the poor heating effect of powder catalysts results in low CO2 reduction efficiency. Herein, a Cu/corncob biochar honeycomb composite was synthesized using a facile impregnation/calcination method. The corncob biochar exhibited a honeycomb morphology with a high specific surface area and abundant adsorption sites due to its porous surface structure. The localized heating and the generation of high-energy hot electrons were facilitated by localized surface plasmon resonance (LSPR) induced by Cu nanoparticles. Consequently, the photothermal catalytic reduction of CO2 was enhanced, significantly contributing to the high conversion of CO2 to methanol in pure water. Notably, 5% wt Cu/corncob biochar showed a CO2 adsorption capacity of 52.59 cm3 g−1 under conditions of 25 °C and 1 bar. Simultaneously, under full-spectrum irradiation, Cu nanoparticles catalyzed the formation of key intermediates, *COOH and *CH3O species, during the CO2 conversion process, resulting in a high CH3OH yield of 63.3 μmol g−1. This work provides a promising strategy to reduce environmental pollution caused by solid waste accumulation and carbon dioxide emissions.

Graphical abstract: Construction of a floatable copper/corncob biochar composite with an LSPR effect for CO2 capture and efficient photothermal catalytic conversion

Supplementary files

Article information

Article type
Research Article
Submitted
30 May 2025
Accepted
15 Jul 2025
First published
16 Jul 2025

Inorg. Chem. Front., 2025, Advance Article

Construction of a floatable copper/corncob biochar composite with an LSPR effect for CO2 capture and efficient photothermal catalytic conversion

H. Gui, Z. Yang, Y. Zhang, T. Huhe and X. Li, Inorg. Chem. Front., 2025, Advance Article , DOI: 10.1039/D5QI01217A

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