Extending the environmental lifetime of unpackaged perovskite solar cells through interfacial design

Language
en
Document Type
Article
Issue Date
2018-01-17
Issue Year
2016
Authors
Chen, Haiwei
Hou, Yi
Halbig, Christian E.
Chen, Shi
Zhang, Hong
Li, Ning
Guo, Fei
Tang, Xiaofeng
Gasparini, Nicola
Levchuk, Ievgen
Editor
Abstract

Solution-processed oxo-functionalized graphene (oxo-G1) is employed to substitute hydrophilic PEDOT:PSS as an anode interfacial layer for perovskite solar cells. The resulting devices exhibit a reasonably high power conversion efficiency (PCE) of 15.2% in the planar inverted architecture with oxo-G1 as a hole transporting material (HTM), and most importantly, deploy the full open-circuit voltage (Voc) of up to 1.1 V. Moreover, oxo-G1 effectively slows down the ingress of water vapor into the device stack resulting in significantly enhanced environmental stability of unpackaged cells under illumination with 80% of the initial PCE being reached after 500 h. Without encapsulation, ∼60% of the initial PCE is retained after ∼1000 h of light soaking under 0.5 sun and ambient conditions maintaining the temperature beneath 30 °C. Moreover, the unsealed perovskite device retains 92% of its initial PCE after about 1900 h under ambient conditions and in the dark. Our results underpin that controlling water diffusion into perovskite cells through advanced interface engineering is a crucial step towards prolonged environmental stability.

Journal Title
Journal of Materials Chemistry A
Volume
4
Issue
30
Citation

Journal of Materials Chemistry A 4.30 (2016): S. 11604-11610. http://pubs.rsc.org/en/content/articlelanding/2016/ta/c6ta03755k

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