4.8 Article

Improving Photocatalytic Water Treatment through Nanocrystal Engineering: Mesoporous Nanosheet-Assembled 3D BiOCI Hierarchical Nanostructures That Induce Unprecedented Large Vacancies

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 52, 期 12, 页码 6872-6880

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.8b00352

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资金

  1. National Natural Science Foundation of China [21425729, 21271108, 21403001, 21701125]
  2. Tianjin Municipal Science and Technology Commission [11JCZDJC24800]
  3. China Postdoctoral Science Foundation [2015M580208]
  4. 111 Program of Ministry of Education of China [T2017002]
  5. Fundamental Research Funds for the Central Universities
  6. NSF ERC on Nanotechnology-Enabled Water Treatment [EEC-1449500]

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Vacancy control can significantly enhance the performance of photocatalytic semiconductors for water purification. However, little is known about the mechanisms and approaches that could generate stable large vacancies. Here, we report a new mechanism to induce vacancy formation on nanocrystals for enhanced photocatalytic activity: the introduction of mesopores. We synthesized two nanosheet-assembled hierarchical 3D BiOCl mesoporous nanostructures with similar morphology and exposed facets but different nanosheet thickness. Positron annihilation analysis detected unprecedentedly large V-'''(BiVOVBiVOVBi''')-V-center dot center dot-V-'''-V-center dot center dot vacancy associates (as well as (VBiVOVBi''')-V-'''-V-center dot center dot) on BiOCl assembled from 3-6 nm nanosheets but only (VBiVOVBi''')-V-'''-V-center dot center dot, vacancy associates on BOICl assemDied rrom thicKer (10-z20 nm nanosneets. Comparison of vacancy properties with 2D ultrathin 2.7 nm nanosheets (with V-Bi'''V-O center dot center dot V-Bi''' and V-Bi''' indicates that nanosheet thinness alone cannot explain the formation of such large atom vacancies. On the basis of density functional theory computations of formation energy of isolated Bi vacancy, we show that mesopores facilitate the formation of large vacancies to counterbalance thermodynamic instability caused by incompletely coordinated Bi and O atoms along the mesopore perimeters. We corroborate that the extraordinarily large V-Bi'''V center dot center dot V-BI'''V-O center dot center dot V-Bi''' vacancy associates facilitate photoexcitation of electrons and prevent the recombination of electron-hole pairs, which significantly enhances photocatalytic activity. This is demonstrated by the rapid mineralization of bisphenol A (10(-S) M) with low photocatalyst loading (l g L-1), as well as enhanced bacterial disinfection. Improved electron-hole separation is also corroborated by enhanced photocatalytic reduction of nitrate.

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