4.8 Article

Enabling full-scale grain boundary mitigation in polycrystalline perovskite solids

Journal

SCIENCE ADVANCES
Volume 8, Issue 35, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.abo3733

Keywords

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Funding

  1. Beijing Natural Science Foundation [JQ21005]
  2. National Key R&D Program of China [2021YFB3800100, 2021YFB3800101]
  3. National Natural Science Foundation of China [91733301, 62104221]
  4. China Postdoctoral Science Foundation [2020M670036]
  5. RD Fruit Fund [20210001]
  6. King Abdulaziz City for Science and Technology (KACST)
  7. Royal Society
  8. EPSRC project SUNRISE [EP/P032591/1]
  9. U.S. Office of Naval Research [N00014-17-1-2241]
  10. USTC Research funds of the Double First-Class Initiative [YD2100002007]
  11. Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]
  12. DOE Office of Science User Facility [DE-AC02-05CH11231]
  13. Generalitat de Catalunya [2017 SGR 327]
  14. Spanish MINECO project [ENE2017-85087-C3]
  15. Severo Ochoa program from Spanish MINECO [SEV-2017-0706]
  16. CERCA Programme/Generalitat de Catalunya

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Researchers have successfully mitigated grain boundaries in perovskite solar cells at both nano and submicron scales, leading to improved device efficiency and stability under various stress conditions.
There exists a considerable density of interaggregate grain boundaries (GBs) and intra-aggregate GBs in polycrystalline perovskites. Mitigation of intra- aggregate GBs is equally notable to that of interaggregate GBs as intra-aggregate GBs can also cause detrimental effects on the photovoltaic performances of perovskite solar cells (PSCs). Here, we demonstrate full-scale GB mitigation ranging from nanoscale intra-aggregate to submicron-scale interaggregate GBs, by modulating the crystallization kinetics using a judiciously designed brominated arylamine trimer. The optimized GB-mitigated perovskite films exhibit reduced nonradiative recombination, and their corresponding mesostructured PSCs show substantially enhanced device efficiency and long-term stability under illumination, humidity, or heat stress. The versatility of our strategy is also verified upon applying it to different categories of PSCs. Our discovery not only specifies a rarely addressed perspective concerning fundamental studies of perovskites at nanoscale but also opens a route to obtain high-quality solution-processed polycrystalline perovskites for high-performance optoelectronic devices.

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