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Graphical abstract Schematic illustration of the formation of CQDs/ZnO@HNTs in the whole synthetic process. Highlights • We have experimentally demonstrated the carbon incorporated ZnO via coupling CQDs. A notable transformation of burger-like CQD s /ZnO morphology was observed and the HNTs have been introduced to improve the dispersity of hybrid photocatalysts. • From efficiently modulation of band structure of CQD s -based materials, the as-prepared CQD s /ZnO@HNTs display a remarkable optical excitation in photogenerated reactive oxygen species (ROS). • This work provides an efficient and novel strategy for element incorporated with introduced inorganic quantum dots owing to the quantum size effect. • It also developed a new sight of CQD s participated phase tuning for semiconductors, offering a beneficial route for expanding the application of VLD photodegradation based on band-tuning semiconductors and other low-dimension materials. Abstract Environmentally friendly photodegradation of refractory pollutants utilizing semiconductor photocatalysis evolution exhibits satisfactory efficiency and low energy consumption, but some of its unbefitting band position largely limits practical applications. The controllable band structure tuning via coupling low-dimensional materials with enormous potential in semiconductor photocatalysis, notably attractive carbon quantum dots (CQDs) induced for a better utilization of low-energy photoexcitation of promising inherent optical properties and photocatalytic performance on organic pollutant degradation. Here, a CQDs modified ZnO hybrid materials was synthesized and the CQDs preluded carbon-incorporated burger-like ZnO nanoparticles clusters were presented thus demonstrated a specific doping-effect. The dispersity improved by loading halloysite nanotube (HNTs) for efficiently photocatalytic activity enhancement. Furthermore, the band structure, excitation and photocatalytic reactive oxygen species (ROS) generation were detected to reveal the photochemical properties and plausible mechanism of CQDs hybrid nanomaterials system. It is observed that the superoxide radical (O 2 −), and singlet oxygen(1O 2) are the principal ROS agents under UV–vis excitations. This work not only displays a CQDs modified system of expanding photo-response range to visible light but also throws a way for quantum elemental incorporated on the influence of band-tuning for semiconductor- dominated photocatalysts. [ABSTRACT FROM AUTHOR]

One of current ideal thought to reduce the recombination of photogenerated electrons and holes from semiconductors is constructing Multi-dimensional semiconductor-carbon (S-C) heterostructures. As well as acting to photo-degrade the organic contaminant and decrease the toxicity, β-In 2 S 3 is chosen as a potential semiconductors for photocatalysts. Relative good photocatalytic properties delivered on β-In 2 S 3 , however, the fast recombination of photogenerated charge carriers are often appeared, causing reduced further application. Carbon quantum dots (CQDs) involve the introduction of plasma effect into the zero-dimensional nanomaterials in order to arouse an effect: either promoting the charge carriers transfer or plasma energy conversion of the photo-excited CQDs. However, state of the two components also encompass the poor quantum yield existed in the CQDs by its serious agglomeration. Thereby, the delivery of extraordinary ballistic electrical and thermal conductivity on single-walled carbon nanotubes (SWNTs), have shown potential for use in a variety of semiconductors decorating application. Herein, we show that a novel CQDs@In 2 S 3 /SWNTs composite in the Multi-dimensional (3D) hierarchical superstructures with an enhanced photocatalytic efficiency. The ESR analysis and free radicals trapping experiments indicated that the O 2 • − and h + were the main active species for the photocatalytic degradation. The potential photocatalytic mechanism of the three components is discussed and the direction in the plasma effect exhibited in CQDs is also considered, with a particular focus on photocatalytic area. [ABSTRACT FROM AUTHOR]