4.6 Article

Ion-migration and carrier-recombination inhibition by the cation-π interaction in planar perovskite solar cells

Journal

ORGANIC ELECTRONICS
Volume 75, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.orgel.2019.105387

Keywords

Perovskite solar cells; Migration of intrinsic ions; Cation-pi interaction

Funding

  1. National Natural Science Foundation of China [51502081, 11504093, 11674144]
  2. Basic Research Projects in Henan Province, China [122300410231]
  3. Marie Curie COFUND fellowship
  4. Welsh Assembly Government
  5. European Union [663830]
  6. Natural Science Foundation of Shandong Province [JQ201602, ZR2018MA038]
  7. EPSRC [EP/N020863/1] Funding Source: UKRI

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In organic-inorganic hybrid perovskite solar cells, migration of intrinsic ions (e.g., MA(+), Pb2+, I-) have a significant impact on the current-voltage hysteresis and stability of devices. Here, N, N'-diphenyl-1, 1'-biphenyl-4, 4'-diamine (NPB) was introduced into MAPbI(3) perovskite layer to facilitate the stability of perovskite film and improved the efficiency of planar perovskite solar cells (PSCs). The results suggest that migration of intrinsic ions are inhibited effectively by cation-pi interaction between NPB and MA(+), and lead to reduce intrinsic defects in perovskite films, which is benefit for the stability of devices. Lewis basicity of NPB enhances the crystallization, passivates the perovskites films and addresses the issue of low electron extraction efficiency. Consequently, solar cells made using NPB modified MAPbI(3) resulted hysteresis-free, enhanced power conversion efficiency of 19.22% with improved stability.

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