TY - JOUR
T1 - Concurrent photocatalytic bicarbonate (aqueous-CO2) reduction and xylose reforming to produce compounds from C—C coupling
AU - Putri, Novy Pralisa
AU - Nguyen, Van Can
AU - Sanoe, Meyta
AU - Lee, Yuh Lang
AU - Teng, Hsisheng
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024/4/15
Y1 - 2024/4/15
N2 - Using CO2 (or aqueous-CO2, HCO3−) and biomass as feedstock to produce chemicals under solar irradiation represents a promising approach to achieving the net-zero emission goal. In this study, we employed a highly efficient •H-forming photocatalyst to convert HCO3−, demonstrating the occurrence of C[sbnd]C coupling to produce C2-species. Under simulated solar illumination, the photocatalytic system consistently reduces HCO3− into acetate through the coupling of •CO2− radicals. Additionally, in the photoreforming of xylose, acetate emerges as the predominant product, likely resulting from the coupling of •CO2− derived from the interaction of formate and •OH. Notably, a C6-compound is generated through C[sbnd]C coupling of radicals originating from HCO3− and xylose. Achieving an overall apparent quantum efficiency of 26% under 420-nm irradiation, our work underscores the feasibility of concurrently photocatalyzing the conversion of CO2 and biomass into chemicals through C[sbnd]C coupling. This study not only highlights the significance of our approach in contributing to the net-zero emission goal but also emphasizes the novelty of achieving concurrent photocatalytic conversion.
AB - Using CO2 (or aqueous-CO2, HCO3−) and biomass as feedstock to produce chemicals under solar irradiation represents a promising approach to achieving the net-zero emission goal. In this study, we employed a highly efficient •H-forming photocatalyst to convert HCO3−, demonstrating the occurrence of C[sbnd]C coupling to produce C2-species. Under simulated solar illumination, the photocatalytic system consistently reduces HCO3− into acetate through the coupling of •CO2− radicals. Additionally, in the photoreforming of xylose, acetate emerges as the predominant product, likely resulting from the coupling of •CO2− derived from the interaction of formate and •OH. Notably, a C6-compound is generated through C[sbnd]C coupling of radicals originating from HCO3− and xylose. Achieving an overall apparent quantum efficiency of 26% under 420-nm irradiation, our work underscores the feasibility of concurrently photocatalyzing the conversion of CO2 and biomass into chemicals through C[sbnd]C coupling. This study not only highlights the significance of our approach in contributing to the net-zero emission goal but also emphasizes the novelty of achieving concurrent photocatalytic conversion.
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U2 - 10.1016/j.cej.2024.150318
DO - 10.1016/j.cej.2024.150318
M3 - Article
AN - SCOPUS:85187790410
SN - 1385-8947
VL - 486
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 150318
ER -