4.3 Article

Template-free fabrication and growth mechanism of uniform (BiO)(2)CO3 hierarchical hollow microspheres with outstanding photocatalytic activities under both UV and visible light irradiation

期刊

JOURNAL OF MATERIALS CHEMISTRY
卷 21, 期 33, 页码 12428-12436

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1jm11840d

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资金

  1. National High Technology Research and Development Program (863 Program) of China [2010AA064905]
  2. Chongqing Technology and Business University [2010-56-13]
  3. Program for Chongqing Innovative Research Team Development in University [KJTD201020]
  4. Chongqing Key Natural Science Foundation (CSTC) [2008BA4012]
  5. Research Grants Council of Hong Kong [PolyU 5204/07E, PolyU 5175/09E]
  6. Hong Kong Polytechnic University [GU712, GYX75, GYX0L]

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The morphology-controlled fabrication of nano-/microstructured functional materials has opened up new possibilities to enhance their physical and chemical properties and remains a great challenge. This work represents a one-pot template-free fabrication and growth mechanism of novel rose-like uniform (BiO)(2)CO3 hierarchical hollow microspheres, which are self-assembled by single-crystal nanosheets. The observation of time-dependent evolution of crystal structure and morphology revealed that the growth mechanism of such a novel structure might involve a unique multistep pathway. First, an amorphous particle was formed during a nucleation and aggregation process. Then, the intermediate (BiO)(4)CO3(OH)(2) of embryonic stacked buds with attached particles were produced due to Ostwald ripening. The driving force for the formation of such embryonic structure is the intrinsic dipole field introduced by the nanosheets as a result of selective adsorption of the citrate ions on some polar surfaces of the nanoparticles. Subsequently, all the particles were consumed and (BiO)(4)CO3(OH)(2) crystals started to transform to (BiO)(2)CO3 phase by means of repeated reaction-dissolution-recrystallization process in a homocentric layer-by-layer growth style, where carbonate ions substituted OH- groups. Monodisperse buds were then generated and the size of the hollow in the center becomes smaller to reduce surface energy. Finally, all (BiO)(4)CO3(OH)(2) transformed to (BiO)(2)CO3 phase and uniform monodisperse (BiO)(2)CO3 roses were produced through layers splitting driven by the OH- group deintercalating from the interlayer spaces of (BiO)(4)CO3(OH)(2). More interestingly, the novel (BiO)(2)CO3 microspheres exhibited outstanding activities under both UV and visible light irradiation for indoor NO removal, far exceeding that of commercial P25, synthetic C-doped TiO2 and (BiO)(2)CO3 with particle morphology due to the special hierarchical morphology and band gap structure.

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