J. Mater. Sci. Technol. ›› 2017, Vol. 33 ›› Issue (7): 728-733.DOI: 10.1016/j.jmst.2016.08.030

• Orginal Article • Previous Articles     Next Articles

Inorganic Nanotube/Organic Nanoparticle Hybrids for

Chen Yingzhi1, Li Aoxiang1, Jin Ming1, Lu-NingWang1,*(), Zheng-HongHuang2   

  1. 1 School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, China
    2 Key Laboratory of Advanced Materials (MOE), School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China
  • Received:2016-06-06 Revised:2016-08-20 Accepted:2016-08-25 Online:2017-07-20 Published:2017-08-29
  • Contact: Lu-NingWang
  • About author:

    These authors contributed equally to this work.

Abstract:

Inorganic/organic nanohybrids composed of arrayed TiO2 nanotubes (TiNTs)/porphyrin nanoparticles (NPs) have been fabricated via a wet chemical approach. The inorganic component, particularly the arrayed one-dimensional (1D) nanostructures, provides high charge-carrier mobility and rapid charge transport. The organic component exhibits extensive visible light absorption and good solution processability. Additionally, the geometric restraint by supramolecular assembly renders an improved photostability. A combination of these two components could thus allow for an efficient solar energy conversion. In this work, a colloid of porphyrin NPs prepared by a solvent exchange method is coated on anodic TiNTs by means of a dip-coating treatment to form inorganic/organic hybrids. The hybrids exhibit an improvement on solar absorption and a significant enhancement on photocurrent generation at a small bias compared with individual component. Herein, the inorganic/organic nanohybrids are proved to be excellent photoanodes highly responsive to visible light and thus pave a way to discover new inorganic/organic assemblies for high-performance optoelectronic applications, as well as for device integration.

Key words: Anodic TiO2 nanotubes, Porphyrin nanoparticles, Inorganic/organic nanohybrid, Photoelectrochemical water splitting