氮化碳
量子点
材料科学
降级(电信)
碳量子点
光催化
碳纤维
可见光谱
光电子学
氮化物
电荷(物理)
调制(音乐)
纳米技术
化学工程
复合材料
化学
复合数
电子工程
催化作用
哲学
工程类
物理
美学
量子力学
生物化学
图层(电子)
作者
Yuanyuan Li,Yuan Si,Bing‐Xin Zhou,Tao Huang,Wei‐Qing Huang,Wangyu Hu,Anlian Pan,Xiaoxing Fan,Gui‐Fang Huang
出处
期刊:Nanoscale
[The Royal Society of Chemistry]
日期:2020-01-01
卷期号:12 (5): 3135-3145
被引量:44
摘要
Steering charge kinetics at the interface is essential to improve the photocatalytic performance of two-dimensional (2D) material-based heterostructures. Herein, we developed a novel strategy-simultaneously building two kinds of heterojunctions- to modulate interfacial charge kinetics in polymeric carbon nitride (CN) for improving the photocatalytic activity. Using a simple one-step thermal condensation of carbon quantum dot (CQD)-contained supramolecular precursors formed in water, the controllable CQD embedded CN nanoframes possessed two kinds of heterogeneous interfaces within seamlessly stitched micro-area two-dimensional in-plane and out-of-plane domains. These two kinds of heterojunctions can effectively enhance its intrinsic driving force to accelerate the separation and transfer of charge along different directions. Furthermore, the hollow double-deck porous CN-CQD nanoframes with a high surface area (296.74 m2 g-1) endowed more exposed active sites. The remarkable visible-light photocatalytic activity of hollow porous CN-CQD nanoframes was demonstrated by degrading tetracycline (TC) and rhodamine (RhB) as the models, whose robust degradation rate constant is approximately 11 and 29 times higher than that of pristine CN, respectively. This work provides a novel strategy for the interfacial design of the heterophase junction with atomic precision.
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