Journal
ADVANCED ENERGY MATERIALS
Volume 8, Issue 31, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.201802346
Keywords
all-inorganic perovskite solar cells; cesium lead bromide halides; grain boundary passivation; perovskite films; rare earth ion doping
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Funding
- National Natural Science Foundation of China [61774139, 21503202]
- Fundamental Research Funds for the Central Universities [11618409]
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All-inorganic cesium lead bromide (CsPbBr3) perovskite solar cells have attracted enormous attention owing to their outstanding stability in comparison with organic-inorganic hybrid devices. The greatest weakness for inorganic CsPbBr3 solar cells is their lower power conversion efficiencies, mainly arising from inferior light-absorbance range and serious charge recombination at interfaces or within perovskite films. To address this issue, the lattice doping of lanthanide ions (Ln(3+) = La3+, Ce3+, Nd3+, Sm3+, Eu3+, Gd3+, Tb3+, Ho3+, Er3+, Yb3+, and Lu3+) into CsPbBr3 films for all-inorganic solar cells free of hole-transporting materials and precious metal electrodes is presented. Arising from the enlarged grain size and prolonged carrier lifetimes upon incorporating Ln(3+) ions into perovskite lattice, the performances of these inorganic CsPbBr3 solar cell devices are significantly enhanced, achieving a champion efficiency as high as 10.14% and an ultrahigh open-circuit voltage of 1.594 V under one sun illumination. Meanwhile, the nearly unchanged efficiency upon persistent attack by 80% RH in air atmosphere over 110 d and enhanced thermal stability at 80 degrees C over 60 d provide new opportunities of promoting commercialization of all-inorganic CsPbBr3 perovskite solar cells.
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