296
Views
1
CrossRef citations to date
0
Altmetric
Articles

Acceptor-donor-acceptor type planar hole-transporting materials for efficient dopant-free perovskite solar cells

, , , & ORCID Icon
Pages 54-59 | Published online: 02 May 2018
 

ABSTRACT

Acceptor-donor-acceptor (A-D-A) type organic small molecule (SM-1) has been explored as an efficient dopant-free hole transporting material (HTM) to replace spiro-OMeTAD in the perovskite solar cells. High quality smooth, uniform, and hydrophobic SM-1 HTM can be readily deposited through solution casting without any external dopants. The highly compatible highest occupied molecular orbital level of −5.15 eV of SM-1 with respect to the perovskite valence band, along with intrinsically rich hole conductive nature effectively extracts holes from perovskite and thereby showed a reasonably high power conversion efficiency of 10.54%. Henceforth, the SM-1 based PSCs results successfully demonstrate the advancement of dopant-free PSCs through design engineering of planar A-D-A type conjugated small molecules.

Additional information

Funding

This work was supported by the National Research Foundation (NRF-2016R1E1A1A01942593) by the Ministry of Science, ICT of Korea. This research was also supported by the Dong-A University Research Fund.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 2,387.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.