TY - JOUR
TI - Avoiding ambient air and light induced degradation in high-efficiency polymer solar cells by the use of hydrogen-doped zinc oxide as electron extraction material
AU - Polydorou, E.
AU - Sakellis, I.
AU - Soultati, A.
AU - Kaltzoglou, A.
AU - Papadopoulos, T.A.
AU - Briscoe, J.
AU - Tsikritzis, D.
AU - Fakis, M.
AU - Palilis, L.C.
AU - Kennou, S.
AU - Argitis, P.
AU - Falaras, P.
AU - Davazoglou, D.
AU - Vasilopoulou, M.
JO - Nano Energy
PY - 2017
VL - 34
TODO - null
SP - 500-514
PB - ELSEVIER SCIENCE LTD.
SN - 2211-2855
TODO - 10.1016/j.nanoen.2017.02.047
TODO - Butyric acid;  Electron transport properties;  Electrons;  Environmental technology;  Extraction;  Grain boundaries;  Hydrogen;  Passivation;  Perovskite solar cells;  Polymer solar cells;  Polymers;  Solar power generation;  Stability;  Surface defects;  Zinc;  Zinc oxide, Commercial applications;  Electron transport materials;  Environmental influences;  Hydrogen doping;  Light-induced degradation;  Long term stability;  Photo-stability;  Photovoltaic performance, Solar cells
TODO - Polymer solar cells have undergone rapid development in recent years. Their limited stability to environmental influence and during illumination, however, still remains a major stumbling block to the commercial application of this technology. Several attempts have been made to address the instability issue, mostly concentrated on the insertion of charge transport interlayers in the device stack. Although zinc oxide (ZnO) is one of the most common electron transport materials in those cells, the presence of defects at the surface and grain boundaries significantly affects the efficiency and stability of the working devices. To address these issues, we herein employ hydrogen-doping of ZnO electron extraction material. It is found that devices based on photoactive layers composed of blends of poly(3-hexylthiophene) (P3HT) with electron acceptors possessing different energy levels, such as [6,6]-phenyl-C70butyric acid methyl ester (PC70BM) or indene-C60 bisadduct (IC60BA) essentially enhanced their photovoltaic performance when using the hydrogen-doped ZnO with maximum power conversion efficiency (PCE) reaching values of 4.62% and 6.65%, respectively, which are much higher than those of the cells with the pristine ZnO (3.08% and 4.51%). Most significantly, the degradation of non-encapsulated solar cells when exposed to ambient or under prolonged illumination is studied and it is found that devices based on un-doped ZnO showed poor environmental stability and significant photo-degradation while those using hydrogen-doped ZnO interlayers exhibited high long-term ambient stability and maintained nearly 80–90% of their initial PCE values after 40 h of 1.5 AM illumination. All mechanisms responsible for this enhanced stability are elucidated and corresponding models are proposed. This work successfully addresses and tackles the instability problem of polymer solar cells and the key findings pave the way for the upscaling of these and, perhaps, of related devices such as perovskite solar cells. © 2017 Elsevier Ltd
ER -