Using time-dependent terahertz spectroscopy, we investigate the role of mixed-cation and mixed-halide on the ultrafast photoconductivity dynamics of two different methylammonium(MA) lead-iodide perovskite thin films. ...Using time-dependent terahertz spectroscopy, we investigate the role of mixed-cation and mixed-halide on the ultrafast photoconductivity dynamics of two different methylammonium(MA) lead-iodide perovskite thin films. It is found that the dynamics of conductivity after photoexcitation reveals significant correlation on the microscopy crystalline features of the samples. Our results show that mixed-cation and lead mixed-halide affect the charge carrier dynamics of the lead-iodide perovskites. In the(5-AVA)_(0.05)(MA)_(0.95) PbI_(2.95) Cl_(0.05)/spiro thin film, we observe a much weaker saturation trend of the initial photoconductivity with high excitation fluence, which is attributed to the combined effect of sequential charge carrier generation, transfer, cooling and polaron formation.展开更多
The metal halide perovskite materials demonstrate outstanding performance in photovoltaics because of their excellent optoelectronic properties (1-7)The perovskite solar cells (PSCs) exhibiting outstanding efficiency ...The metal halide perovskite materials demonstrate outstanding performance in photovoltaics because of their excellent optoelectronic properties (1-7)The perovskite solar cells (PSCs) exhibiting outstanding efficiency [8,9], high power-per-weight [10], and excellent radiation resistance[11-13] are considered to be promising for developing the new-generation energy technology for space application.展开更多
As perovskite solar cells show tremendous potential for widespread applications, we find that adding inorganic thermal-stable cesium ions into MAPbI_3 results in significantly improves thermal stability. For un-encaps...As perovskite solar cells show tremendous potential for widespread applications, we find that adding inorganic thermal-stable cesium ions into MAPbI_3 results in significantly improves thermal stability. For un-encapsulated perovskite devices, the energy conversion efficiency maintains about 75% of its original value(over 15%) in the MA_(0.85)Cs_(0.05)PbI_3 device under 80 min of heating at 140°C in a dry atmosphere(RH ≤ 30%). With significantly improved thermal stability achieved by a convenient process, it is expected that this type of mixed-cation perovskites can further facilitate large scale applications.展开更多
FA-Cs mixed-cation perovskite has been reported as a promising candidate for obtaining highly efficient and stable photovoltaic devices.Phenylethylamine iodide(PEAI)post-treatment is a widely used and effective method...FA-Cs mixed-cation perovskite has been reported as a promising candidate for obtaining highly efficient and stable photovoltaic devices.Phenylethylamine iodide(PEAI)post-treatment is a widely used and effective method for surface passivation of FA-Cs perovskite layer in devices.However,it is still controversial whether the PEAI post-treatment would form two-dimensional(2D)perovskite PEA_(2)PbI_(4) capping layer or just result in PEA+terminated surface.Here in this work,the function of PEAI post-treatment on FA-Cs mixed-cation perovskite FA_(1-x)Cs_(x)PbI_(3)(x=0.1–0.9)with varied Cs contents is elucidated.With increased Cs content,the FA-Cs perovskite shows higher resistance to the cation exchange between FA+and PEA+.This Cs-content-dependent cation exchange results in the different PEAI reaction preferences with FA-Cs mixed-cation perovskites.Furthermore,higher Cs content with stronger resistance to cation exchange reaction leads to a wider processing window for post-treatment and defect passivation,which is beneficial for the fabrication of large-scale photovoltaic devices.展开更多
基金Supported by the National Natural Science Foundation of China under Grant Nos 11604202,11674213,61735010 and 51603119the Young Eastern Scholar under Grant Nos QD2015020 and QD2016027+3 种基金the Shanghai Rising-Star Program under Grant No18QA1401700the ‘Chen Guang’ Project under Grant Nos 16CG45 and 16CG46the Shanghai Municipal Education Commissionthe Shanghai Education Development Foundation
文摘Using time-dependent terahertz spectroscopy, we investigate the role of mixed-cation and mixed-halide on the ultrafast photoconductivity dynamics of two different methylammonium(MA) lead-iodide perovskite thin films. It is found that the dynamics of conductivity after photoexcitation reveals significant correlation on the microscopy crystalline features of the samples. Our results show that mixed-cation and lead mixed-halide affect the charge carrier dynamics of the lead-iodide perovskites. In the(5-AVA)_(0.05)(MA)_(0.95) PbI_(2.95) Cl_(0.05)/spiro thin film, we observe a much weaker saturation trend of the initial photoconductivity with high excitation fluence, which is attributed to the combined effect of sequential charge carrier generation, transfer, cooling and polaron formation.
基金supported by the National Basic Research Program of China(Grant No.2015CB932203)the National Natural Science Foundation of China(Grant Nos.61722501,and 61377025)+2 种基金the Beijing Natural Science Foundation(Grant No.4164106)the Scientific Experimental System in Near Space of Chinese Academy of Sciences(Grant No.XDA17000000)the General Financial Grant from the China Postdoctoral Science Foundation(Grant No.2017M620519)
文摘The metal halide perovskite materials demonstrate outstanding performance in photovoltaics because of their excellent optoelectronic properties (1-7)The perovskite solar cells (PSCs) exhibiting outstanding efficiency [8,9], high power-per-weight [10], and excellent radiation resistance[11-13] are considered to be promising for developing the new-generation energy technology for space application.
基金jointly supported by the State Key Program for Basic Research of China(No.2015CB659300)the National Natural Science Foundation of China(Nos.11621091 and 11574143)+2 种基金the Natural Science Foundation of Jiangsu Province(Nos.BK20150056)the Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)the Fundamental Research Funds for the Central Universities
文摘As perovskite solar cells show tremendous potential for widespread applications, we find that adding inorganic thermal-stable cesium ions into MAPbI_3 results in significantly improves thermal stability. For un-encapsulated perovskite devices, the energy conversion efficiency maintains about 75% of its original value(over 15%) in the MA_(0.85)Cs_(0.05)PbI_3 device under 80 min of heating at 140°C in a dry atmosphere(RH ≤ 30%). With significantly improved thermal stability achieved by a convenient process, it is expected that this type of mixed-cation perovskites can further facilitate large scale applications.
基金supported by the National Key Research and Development Program of China(2017YFE0127100)the National Natural Science Foundation of China(NSFC,Grant 22025505)+1 种基金the Program of Shanghai Academic Technology Research Leader(Grant 20XD1422200)the Key Laboratory of Resource Chemistry,Ministry of Education(KLRC_ME2003)。
文摘FA-Cs mixed-cation perovskite has been reported as a promising candidate for obtaining highly efficient and stable photovoltaic devices.Phenylethylamine iodide(PEAI)post-treatment is a widely used and effective method for surface passivation of FA-Cs perovskite layer in devices.However,it is still controversial whether the PEAI post-treatment would form two-dimensional(2D)perovskite PEA_(2)PbI_(4) capping layer or just result in PEA+terminated surface.Here in this work,the function of PEAI post-treatment on FA-Cs mixed-cation perovskite FA_(1-x)Cs_(x)PbI_(3)(x=0.1–0.9)with varied Cs contents is elucidated.With increased Cs content,the FA-Cs perovskite shows higher resistance to the cation exchange between FA+and PEA+.This Cs-content-dependent cation exchange results in the different PEAI reaction preferences with FA-Cs mixed-cation perovskites.Furthermore,higher Cs content with stronger resistance to cation exchange reaction leads to a wider processing window for post-treatment and defect passivation,which is beneficial for the fabrication of large-scale photovoltaic devices.