4.8 Article

N-doped carbon quantum dots for TiO2-based photocatalysts and dye-sensitized solar cells

Journal

NANO ENERGY
Volume 2, Issue 5, Pages 545-552

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nanoen.2013.07.010

Keywords

N-doped carbon quantum dots/TiO2; Photosensitizers; Photocatalysis; Dye-sensitized solar cell

Funding

  1. NSFC [51002107, 21173159, 61106125, 51025207]
  2. NSFZJ [Y4090118]
  3. Top Key Discipline [100061200119]
  4. ZJSTD Key Innovative Team [2012R10014-07]
  5. ZJED Innovative Team

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N-doped nanostructured carbon materials have attracted much attention because the doping can induce new unique physical and chemical properties of carbon. In this study, we report, for the first time, that N-doped carbon quantum dots (NCQDs) can combine with rutile TiO2 and form NCQD5/TiO2 hierarchical microspheres assembled by nanorods with enhanced photocatalytic activities under visible light irradiation. As a result, the pseudo-first-order reaction constant for the degradation of rhodamine B (RhB) on NCQDs/TiO2 (0.11 min(-1)) is 215.7, 7.3 and 1.3 times much larger than that of NCQDs (0.00051 min(-1)), TiO2 (0.015 min(-1)), and CQDs/TiO2 (0.086 min(-1)), respectively. The functions of NCQDs were discussed and a new synergistic photosensitized mechanism was proposed for the degradation of RhB on the as-synthesized NCQD5/TiO2 nanocomposites based on the experimental results. NCQDs were also applied as metal-free sensitizers in dye-sensitized solar cells (DSSCs) for the first time. A preliminary study shows that under one sun illumination (AM 1.5), the open circuit voltage and fill factor values reach 0.46 V and 43%, respectively, achieving a power conversion efficiency of 0.13% in the proof-of-concept TiO2-based DSSCs device. The performance of NCQDs sensitized solar cells surpasses that of N-free counterpart as well. N-doping lowered the work function of CQDs, which was responsible for enhanced photocatalytic activity of NCQD5/TiO2 and better NCQDs sensitized TiO2-based solar cell performance. (C) 2013 Elsevier Ltd. All rights reserved.

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