光降解
光催化
乙醛
材料科学
离子液体
石墨烯
光化学
化学工程
吸附
离子键合
催化作用
激进的
化学
纳米技术
有机化学
离子
乙醇
工程类
作者
Syed Jalil Shah,Xinqi Luan,Xing Yu,Wenming Su,Yucheng Wang,Zhongxing Zhao,Zhenxia Zhao
标识
DOI:10.1016/j.jcis.2024.02.167
摘要
The development of metal organic framework (MOF)-based π-π conjugated structures capable of effectively transforming H2O from humid air to •OH radicals for VOCs photodegradation is a significant but difficult task. Herein, an amino-ionic liquid (NH2-IL) based dual-mode bridging strategy was proposed to connect 3D-graphene with NH2-MIL-125 forming IL-3DGr/NM(Ti) nanohybrids for advanced acetaldehyde photodegradation. The rational integration of these components was responsible for: (1) maintaining π-π conjugated electron transport system; (2) generating abundant coordinatively unsaturated sites and oxygen vacancies; (3) increasing surface area of the nanohybrids. With these attributes, IL-3DGr/NM(Ti) demonstrated enhanced charge separation and transportation electrochemical impedance spectroscopy (EIS): 7-times), acetaldehyde adsorption (22 %), light absorption (bandgap: 1.51 eV). The rapid H2O adsorption and photoconversion to •OH radicals by IL-3DGr/NM(Ti) enabled it to demonstrate superior CH3CHO photodegradation rate under high humidity, surpassing many state-of-the-art photocatalysts by 9 to 187 times under static air conditions and with nearly similar catalyst dosages* (photocatalyst weight and initial acetaldehyde concentration (mg ppm-1) ratio). Interestingly, the IL-3DGr/NM(Ti) photocatalytic activity was enhanced by increasing RH% up-to 80 %. Besides, the nanohybrids demonstrated tremendous stability, with only a 3.9 % decline observed after 5 consecutive-cycles. This strategy provides new prospects to improve the compatibility of graphene/MOF materials for futuristic photoelectrical applications under high humidity.
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