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CuInS2 quantum dots anchored onto the three-dimensional flexible self-supporting graphene oxide array with regulatable crystallinity and defect density for efficient photocatalytic synthesis of xylonic acid

光催化 石墨烯 结晶度 量子点 氧化物 纳米技术 化学 材料科学 有机化学 复合材料 催化作用
作者
Kangning Liu,Zhendong Liu,Shuangquan Yao,Shaolong Sun,Jiliang Ma,Run‐Cang Sun
出处
期刊:Applied Catalysis B-environmental [Elsevier]
卷期号:316: 121573-121573 被引量:28
标识
DOI:10.1016/j.apcatb.2022.121573
摘要

Photocatalytic biorefinery is receiving increasing attention as a promising approach for biomass utilization. In this field, I-III-VI quantum dots have emerged as efficient photocatalysts with unique physical and chemical properties that stem from their quantum and size effects. To fully exploit the advantages of quantum dots, a three-dimensional flexible self-supporting material (CIS@FSM) is fabricated with the assistance of defect-rich graphene oxide (GO), which is employed as a supporter to trap the quantum dots and promote charge separation/migration. Under visible-light irradiation, a xylonic acid yield of 65.05 % is obtained and no obvious decline of the photocatalytic performance is observed after nine runs. Moreover, the photocatalytic performance of CIS@FSM can be tuned by modulating the crystallinity and defect density. The investigation of the mechanism of the xylonic acid production reveals the presence of all oxidation active species, with h + playing the primary role. This work provides insights for semiconductor-based photocatalytic biorefinery. CuInS 2 quantum dots anchored onto the three-dimensional flexible self-supporting graphene oxide array with regulatable crystallinity and defect density for efficient photocatalytic synthesis of xylonic acid. • A novel flexible 3D self-supporting material was prepared by a facile method. • Quantum effect of CuInS 2 quantum dots led to good electrical properties. • GO and annealing led to more efficient light absorption at NIR. • Crystallinity and defect density were easily modulated for good catalytic activity.
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