Lending triarylphosphine oxide to phenanthroline: A Facile approach to high-performance organic small-molecule cathode interfacial material for organic photovoltaics utilizing air-stable cathodes

Wan Yi Tan, Rui Wang, Min Li, Gang Liu, Ping Chen, Xin Chen Li, Shun Mian Lu, Hugh Lu Zhu, Qi Ming Peng, Xu Hui Zhu, Wei Chen, Wallace C.H. Choy, Feng Li, Junbiao Peng, Yong Cao

Research output: Contribution to journalArticlepeer-review

104 Scopus citations

Abstract

Cathode interfacial material (CIM) is critical to improving the power conversion efficiency (PCE) and long-term stability of an organic photovoltaic cell that utilizes a high work function cathode. In this contribution, a novel CIM is reported through an effective and yet simple combination of triarylphosphine oxide with a 1,10-phenanthrolinyl unit. The resulting CIM possesses easy synthesis and purification, a high T g of 116 C and attractive electron-transport properties. The characterization of photovoltaic devices involving Ag or Al cathodes shows that this thermally deposited interlayer can considerably improve the PCE, due largely to a simultaneous increase in V oc and FF relative to the reference devices without a CIM. Notably, a PCE of 7.51% is obtained for the CIM/Ag device utilizing the active layer PTB7:PC71BM, which far exceeds that of the reference Ag device and compares well to that of the Ca/Al device. The PCE is further increased to 8.56% for the CIM/Al device (with J sc = 16.81 mA cm-2, V oc = 0.75 V, FF = 0.68). Ultraviolet photoemission spectroscopy studies reveal that this promising CIM can significantly lower the work function of the Ag metal as well as ITO and HOPG, and facilitate electron extraction in OPV devices.

Original languageEnglish
Pages (from-to)6540-6547
Number of pages8
JournalAdvanced Functional Materials
Volume24
Issue number41
DOIs
StatePublished - 5 Nov 2014
Externally publishedYes

Keywords

  • cathode interfacial materials
  • organic photovoltaics
  • organic small molecules
  • phenanthroline
  • phosphine oxide

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