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作 者:Guangbiao Cao Haoran Xing Haoguan Gui Chao Yao Yinjuan Chen Yongsheng Chen Xiazhang Li
机构地区:[1]National-local Joint Engineering Research Center of Biomass Refining and High-quality Utilization,Changzhou University,Changzhou 213164,China [2]School of Civil and Environmental Engineering,Georgia Institute of Technology,Atlanta,GA 30332-0373,USA
出 处:《Nano Research》2024年第6期5061-5072,共12页纳米研究(英文版)
基 金:the National Natural Science Foundation of China(No.51674043);Jiangsu High Institutions Key Basic Research Projects of Natural Science(No.21KJA430002);Changzhou International Cooperation Project(No.CZ20230018);International Joint Laboratory of the Jiangsu Education Department.
摘 要:Simultaneous conversion of CO_(2)and biomass into value-added chemicals through solar-driven catalysis holds tremendous importance for fostering a sustainable circular economy.Herein,plasmonic Bi quantum dots were immobilized on phosphoric acid modified attapulgite(P-ATP)nanorod using an in-situ reduction-deposition method,and were employed for photocatalytic reduction of CO_(2)coupled with oxidation of biomass-derived benzyl alcohol.Results revealed that Bi atoms successfully integrated into the basal structure of P-ATP,forming chemically coordinated Bi-O-Si bonds that served as efficient transportation channels for electrons.The incorporation of high-density monodispersed Bi quantum dots induced a surface plasmon resonance(SPR)effect,expanding the light absorption range into the near-infrared region.As a consequence,the photo-thermal transformation was significantly accelerated,leading to enhanced reaction kinetics.Notably,50%Bi/P-ATP nanocomposite exhibited the highest plasmon-mediated photocatalytic CH4 generation(115.7μmol·g^(−1)·h^(−1))and CO generation(44.9μmol·g^(−1)·h^(−1)),along with remarkable benzaldehyde generation rate of 79.5μmol·g^(−1)·h^(−1)in the photo-redox coupling system under solar light irradiation.The hydrogen protons released from the oxidation of benzyl alcohol facilitated the incorporation of more hydrogen protons into CO_(2)to form key CH_(3)O−intermediates.This work demonstrates the synergistic solar-driven valorization of CO_(2)and biomass using natural mineral based catalyst.
关 键 词:photothermal catalysis clay mineral PLASMON CO_(2)reduction biomass conversion
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