7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Large, solution-processable graphene quantum dots as light absorbers for photovoltaics.

      1 , , ,
      Nano letters
      American Chemical Society (ACS)

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Graphenes have very attractive properties for photovoltaics. Their tunable bandgap and large optical absorptivity are desirable for efficient light harvesting. Their electronic levels and interfacing with other materials for charge transfer processes can both be tuned with well-developed carbon chemistry. Graphenes have also been shown to have very large charge mobilities, which could be useful for charge collection in solar cells. In addition, they consist of elements abundant on Earth and are environmentally friendly. However, these important properties have not been taken advantage of because graphenes that are large enough to be useful for photovoltaics have extremely poor solubility and have a strong tendency to aggregate into graphite. Here we present a novel solubilization strategy for large graphene nanostructures. It has enabled us to synthesize solution-processable, black graphene quantum dots with uniform size through solution chemistry, and we show that they can be used as sensitizers for solar cells.

          Related collections

          Author and article information

          Journal
          Nano Lett
          Nano letters
          American Chemical Society (ACS)
          1530-6992
          1530-6984
          May 12 2010
          : 10
          : 5
          Affiliations
          [1 ] Department of Chemistry, Indiana University, Bloomington, Indiana 47405, USA.
          Article
          10.1021/nl101060h
          20377198
          882a90ba-ba32-4649-9d8d-d045ab197086
          History

          Comments

          Comment on this article