4.8 Article

Crystallization Kinetics of Organic-Inorganic Trihalide Perovskites and the Role of the Lead Anion in Crystal Growth

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 137, 期 6, 页码 2350-2358

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja512117e

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资金

  1. U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0010560]
  2. Singapore Energy Innovation Program Office
  3. NSF Materials Research Science and Engineering Centers (MRSEC) program [DMR-1120296]
  4. NSF
  5. NIH/National Institute of General Medical Sciences under NSF [DMR-0936384, DMR-1332208]
  6. King Abdullah University of Science and Technology (KAUST) [KUS-C1-018-02]
  7. EPSRC Supergen, ERC Hyper Project
  8. EPSRC [EP/M024881/1] Funding Source: UKRI
  9. Engineering and Physical Sciences Research Council [EP/M024881/1] Funding Source: researchfish

向作者/读者索取更多资源

Methylammonium lead halide perovskite solar cells continue to excite the research community due to their rapidly increasing performance which, in large part, is due to improvements in film morphology. The next step in this progression is control of the crystal morphology which requires a better fundamental understanding of the crystal growth. In this study we use in situ X-ray scattering data to study isothermal transformations of perovskite films derived from chloride, iodide, nitrate, and acetate lead salts. Using established models we determine the activation energy for crystallization and find that it changes as a function of the lead salt. Further analysis enabled determination of the precursor composition and showed that the primary step in perovskite formation is removal of excess organic salt from the precursor. This understanding suggests that careful choice of the lead salt will aid in controlling crystal growth, leading to superior films and better performing solar cells.

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