4.8 Article

Increased Quantum Dot Loading by pH Control Reduces Interfacial Recombination in Quantum-Dot-Sensitized Solar Cells

期刊

ACS NANO
卷 9, 期 8, 页码 8321-8334

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.5b02853

关键词

charge transfer; SILAR; lead sulfide; titanium dioxide; quantum dot; surface coverage; nanostructured solar cells

资金

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0001060]
  2. U.S. Department of Energy through the Bay Area Photovoltaic Consortium [DE-EE0004946]

向作者/读者索取更多资源

The power conversion efficiency of quantum-dot-sensitized solar cells (QDSSCs) hinges on interfacial charge transfer. Increasing quantum dot (QD) loading on the TiO2 anode has been proposed as a means to block recombination of electrons in the TiO2 to the hole transport material; however, it is not known whether a corresponding increase in QD-mediated recombination processes might lead to an overall higher rate of recombination. In this work, a 3-fold increase in PbS QD loading was achieved by the addition of an aqueous base to negatively charge the TiO2 surface during Pb cation deposition. Increased QD loading improved QDSSC device efficiencies through both increased light absorption and an overall reduction in recombination. Unexpectedly, we also found increased QD size had the detrimental effect of increasing recombination. Kinetic modeling of the effect of QD size on interfacial charge transfer processes provided qualitative agreement with the observed variation in recombination lifetimes. These results demonstrate a robust method of improving QD loading, identify the specific mechanisms by which increased QD deposition impacts device performance, and provide a framework for future efforts optimizing the device architecture of QDSSCs.

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