Boosting the efficiency and the stability of low cost perovskite solar cells by using CuPc nanorods as hole transport material and carbon as counter electrode
2016 (English)In: Nano Energy, ISSN 2211-2855, Vol. 20, 108-116 p.Article in journal (Refereed) PublishedText
Low temperature printable carbon cathode based perovskite solar cell was for the first time interfacial engineered with dopant free, nanorod-liked copper phthalocyanine (CuPc) to facilitate charge transportation. Both the CuPc and low temperature processed carbon are potentially noble metal-free and highly stable. By incorporating CuPc nanorods as hole-selective contact material, together with the printable low temperature processed carbon as cathode material, considerably high power conversion efficiency (PCE) of 16.1% was successfully obtained, which is comparable to or even a little higher than the device with state-of-the-art doped spiro-OMeTAD as HTM and noble metal Au as back electrode. Moreover, dramatically enhanced durability relative to doped-spiro-OMeTAD/Au based device was demonstrated by this newly developed device. Detailed excellent capability in accelerating charge extraction and suppressing charge recombination can be disclosed with steady state and time-resolved photoluminescence analysis and electrochemical impedance spectroscopy. To the best our knowledge, this is the highest efficiency that has been reported for PSCs based carbon counter electrode. The work presented here demonstrates an important step forwards to practical applications for PSCs, as it paves the way for developments of cost-effective, stable but still highly efficient PSCs, and offers the promise for a low-cost, mass-manufacturable technology that is compatible with current large-scale printing infrastructure.
Place, publisher, year, edition, pages
Elsevier, 2016. Vol. 20, 108-116 p.
Carbon counter electrode, Copper phthalocyanine nanorod, Hole transport material, Perovskite solar cell
IdentifiersURN: urn:nbn:se:kth:diva-180937DOI: 10.1016/j.nanoen.2015.11.034ISI: 000370468300012ScopusID: 2-s2.0-84952925619OAI: oai:DiVA.org:kth-180937DiVA: diva2:897615
QC 20160126. QC 201603192016-01-262016-01-252016-03-19Bibliographically approved