Although tin halide perovskite has shown excellent photoelectric performance, its efficiency of solar cell is low compared with that of lead halide. In order to enhance the efficiency of tin halide perovskite solar ce...Although tin halide perovskite has shown excellent photoelectric performance, its efficiency of solar cell is low compared with that of lead halide. In order to enhance the efficiency of tin halide perovskite solar cell, a deep understanding of the role of the defects in the perovskite absorption layer and at the electron transport layer(ETL)/absorber or absorber/hole transport layer(HTL) interface is very necessary. In this work, the planar heterojunction-based CH_3NH_3SnI_3 perovskite solar cells were simulated with the SCAPS-1D program. Simulation results revealed a great dependence of device efficiency on defect density and interface quality of the perovskite absorber. The defect density at the front interface is critical for high efficiency, and the polarity of the interface charge has a different impact on the device efficiency. Strikingly, an efficiency over 29% was obtained under the moderate simulation conditions.展开更多
Owing to the combined features of sub-1.4 eV bandgap and all-inorganic composition,cesium tin–lead(Sn-Pb)triiodide perovskite is promising for approaching the Shockley-Queisser limit of solar cells while avoiding the...Owing to the combined features of sub-1.4 eV bandgap and all-inorganic composition,cesium tin–lead(Sn-Pb)triiodide perovskite is promising for approaching the Shockley-Queisser limit of solar cells while avoiding the use of volatile organic cations.But the low Sn(Ⅱ)stability in this perovskite remains a hurdle for delivering its theoretically attainable device performance.Herein we present a synthesis method of this perovskite based on an acetylhydrazine-incorporated antioxidative solution system.Mechanistic investigation shows that acetylhydrazine effectively reduces the oxidation of solution-phase Sn(Ⅱ)and meanwhile creates an electron-rich,protective nano-environment for solid-state Sn(Ⅱ)ions.These lead to high oxidation resistance of the final film as well as effective defect inhibition.The resultant solar cells demonstrate power conversion efficiencies up to 15.04%,the highest reported so far for inorganic perovskite devices with sub-1.4 eV bandgaps.Furthermore,the T_(90) lifetime of these devices can exceed 1000 hours upon light soaking in a nitrogen atmosphere,demonstrating the potential advantage when lower-bandgap perovskite solar cells go all-inorganic.展开更多
基金supported by the Zhejiang Provincial Natural Science Foundation of China (No. LY17F040001)the Technology Development Project Program of Hengdian Group DMEGC Magnetics Co., Ltd (No. 2016330001002138)+1 种基金the Open Project Program of Surface Physics Laboratory (National Key Laboratory) of Fudan University (No. KF2015_02)the Open Project Program of National Laboratory for Infrared Physics, Chinese Academy of Sciences (No. M201503)
文摘Although tin halide perovskite has shown excellent photoelectric performance, its efficiency of solar cell is low compared with that of lead halide. In order to enhance the efficiency of tin halide perovskite solar cell, a deep understanding of the role of the defects in the perovskite absorption layer and at the electron transport layer(ETL)/absorber or absorber/hole transport layer(HTL) interface is very necessary. In this work, the planar heterojunction-based CH_3NH_3SnI_3 perovskite solar cells were simulated with the SCAPS-1D program. Simulation results revealed a great dependence of device efficiency on defect density and interface quality of the perovskite absorber. The defect density at the front interface is critical for high efficiency, and the polarity of the interface charge has a different impact on the device efficiency. Strikingly, an efficiency over 29% was obtained under the moderate simulation conditions.
基金supported by the NSFC(U2001217,21972006)the Shenzhen Peacock Plan(KQTD2016053015544057)+4 种基金the Shenzhen-Hong Kong Innovation Circle United Research Project(SGLH20180622092406130)the Shenzhen Fundamental Research Program(JCYJ20190813105205501)the Research Fund Program of Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices(2019B121203003)the Early Career Scheme(22300221)from the Hong Kong Research Grant Council and the start-up grants,Initiation Grant Faculty Niche Research Areas(IG-FNRA)2020/21,Interdisciplinary Matching Scheme 2020/21,startup grants of the Hong Kong Baptist University(HKBU)the China Postdoctoral Science Foundation(2021M690193)。
文摘Owing to the combined features of sub-1.4 eV bandgap and all-inorganic composition,cesium tin–lead(Sn-Pb)triiodide perovskite is promising for approaching the Shockley-Queisser limit of solar cells while avoiding the use of volatile organic cations.But the low Sn(Ⅱ)stability in this perovskite remains a hurdle for delivering its theoretically attainable device performance.Herein we present a synthesis method of this perovskite based on an acetylhydrazine-incorporated antioxidative solution system.Mechanistic investigation shows that acetylhydrazine effectively reduces the oxidation of solution-phase Sn(Ⅱ)and meanwhile creates an electron-rich,protective nano-environment for solid-state Sn(Ⅱ)ions.These lead to high oxidation resistance of the final film as well as effective defect inhibition.The resultant solar cells demonstrate power conversion efficiencies up to 15.04%,the highest reported so far for inorganic perovskite devices with sub-1.4 eV bandgaps.Furthermore,the T_(90) lifetime of these devices can exceed 1000 hours upon light soaking in a nitrogen atmosphere,demonstrating the potential advantage when lower-bandgap perovskite solar cells go all-inorganic.
