4.7 Article

Impact of the organic halide salt on final perovskite composition for photovoltaic applications

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APL MATERIALS
卷 2, 期 8, 页码 -

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AMER INST PHYSICS
DOI: 10.1063/1.4886275

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资金

  1. National Science Foundation through Materials World Network [DMR-1008125, DMR 1210304]
  2. Singapore Energy Innovation Programme Office
  3. NSF Materials Research Science and Engineering Centers (MRSEC) program [DMR-1120296]
  4. Cornell High Energy Synchrotron Source (CHESS) - NSF
  5. NIH/National Institute of General Medical Sciences under NSF [DMR-0936384]
  6. KAUST-Cornell Center for Energy and Sustainability - King Abdullah University of Science and Technology (KAUST) [KUS-C1-018-02]
  7. Direct For Mathematical & Physical Scien
  8. Division Of Materials Research [1210304] Funding Source: National Science Foundation
  9. Division Of Materials Research
  10. Direct For Mathematical & Physical Scien [1008125] Funding Source: National Science Foundation

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The methylammonium lead halide perovskites have shown significant promise as a low-cost, second generation, photovoltaic material. Despite recent advances, however, there are still a number of fundamental aspects of their formation as well as their physical and electronic behavior that are not well understood. In this letter we explore the mechanism by which these materials crystallize by testing the outcome of each of the reagent halide salts. We find that components of both salts, lead halide and methylammonium halide, are relatively mobile and can be readily exchanged during the crystallization process when the reaction is carried out in solution or in the solid state. We exploit this fact by showing that the perovskite structure is formed even when the lead salt's anion is a non-halide, leading to lower annealing temperature and time requirements for film formation. Studies into these behaviors may ultimately lead to improved processing conditions for photovoltaic films. (C) 2014 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 Unported License.

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