The interface defects between the electron transport layer(ETL)and the perovskite layer,as well as the low ultraviolet(UV)light utilization rate of the perovskite absorption layer,pose significant challenges for the c...The interface defects between the electron transport layer(ETL)and the perovskite layer,as well as the low ultraviolet(UV)light utilization rate of the perovskite absorption layer,pose significant challenges for the commercialization of perovskite solar cells(PSCs).To address this issue,this paper proposes an innovative multifunctional interface modulation strategy by introducing aggregation-induced emission(AIE)molecule 5-[4-[1,2,2-tri[4-(3,5-dicarboxyphenyl)phenyl]ethylene]phenyl]benzene-1,3-dicarboxylic acid(H_(8)ETTB)at the SnO_(2)ETL/perovskite interface.Firstly,the interaction of H_(8)ETTB with the SnO_(2)surface,facilitated by its carboxyl groups,is effective in passivating surface defects caused by noncoord inated Sn and O vacancies.This interaction enhances the conductivity of the SnO_(2)film and adjusts energy levels,leading to enhanced charge carrier transport.Simultaneously,H_(8)ETTB can passivate noncoord inated Pb^(2+)ions at the perovskite interface,promoting perovskite crystallization and reducing the interface energy barrier,resulting in a perovskite film with low defects and high crystalline quality.More importantly,the H_(8)ETTB molecule,can convert UV light into light absorbable by the perovskite,thereby reducing damage caused by UV light and improving the device's utilization of UV.Consequently,the champion PSC based on SnO_(2)-H_(8)ETTB achieves an impressing efficiency of 23.32%and significantly improved photostability compared with the control device after continuous exposure to intense UV radiation.In addition,the Cs_(0.05)(FA_(0.95)MA_(0.05))_(0.95)Pb(I_(0.95)Br_(0.05))_(3)based device can achieve maximum efficiency of 24.01%,demonstrating the effectiveness and universality of this strategy.Overall,this innovative interface bridging strategy effectively tackles interface defects and low UV light utilization in PSCs,presenting a promising approach for achieving highly efficient and stable PSCs.展开更多
Double perovskites(DPs)with Cs_(2)AgInCl_(6) composition,as one of the lead-free perovskites,have been in the spotlight owing to their intriguing optical properties,namely,self-trapped exciton(STE)emission and dopant-...Double perovskites(DPs)with Cs_(2)AgInCl_(6) composition,as one of the lead-free perovskites,have been in the spotlight owing to their intriguing optical properties,namely,self-trapped exciton(STE)emission and dopant-induced photoluminescence.However,the current DPs still face the challenge of low photoluminescence efficiency and cannot be applied in practice.Herein,we synthesize the Bi^(3+)and Eu^(3+)codoped Cs_(2)AgInCl_(6) DPs,which displays enhanced STE and Eu^(3+)ions characteristic emissions.Our results indicate that the Eu^(3+)ions mainly substitute the In sites and can increase the radiative recombination rate and exciton binding energy of STEs,which is discovered that Eu^(3+)ions can promote the localization of STEs by breaking the inversion symmetry of the Cs_(2)AgInCl_(6) lattice.The existence of Bi^(3+)ions decreases the excitation(absorption)energy,provides a new absorption channel,and increases the energy transfer rate to Eu^(3+)ions.Through adjusting the Bi^(3+)and Eu^(3+)concentrations,a maximum photoluminescence quantum yield of 80.1%is obtained in 6%Eu^(3+)and 0.5%Bi^(3+)codoped Cs_(2)AgInCl_(6) DPs.Finally,the high-quality single-component white-light-emitting diodes based on Bi^(3+)and Eu^(3+)codoped Cs_(2)AgInCl_(6) DPs and a 410-nm commercial ultraviolet chip are fabricated with the optimum color rendering index of 89,the optimal luminous efficiency of 88.1 lm/W,and a half-lifetime of 1,493 h.This work puts forward an effective lanthanide and transition metals codoping strategy to design single-component white-light emitter,taking a big step forward for the application lead-free DPs.展开更多
基金finically supported by the National Natural Science Foundation of China(62350054,12374379,12174152,12304462)the Foundation of National Key Laboratory(***202302011)。
文摘The interface defects between the electron transport layer(ETL)and the perovskite layer,as well as the low ultraviolet(UV)light utilization rate of the perovskite absorption layer,pose significant challenges for the commercialization of perovskite solar cells(PSCs).To address this issue,this paper proposes an innovative multifunctional interface modulation strategy by introducing aggregation-induced emission(AIE)molecule 5-[4-[1,2,2-tri[4-(3,5-dicarboxyphenyl)phenyl]ethylene]phenyl]benzene-1,3-dicarboxylic acid(H_(8)ETTB)at the SnO_(2)ETL/perovskite interface.Firstly,the interaction of H_(8)ETTB with the SnO_(2)surface,facilitated by its carboxyl groups,is effective in passivating surface defects caused by noncoord inated Sn and O vacancies.This interaction enhances the conductivity of the SnO_(2)film and adjusts energy levels,leading to enhanced charge carrier transport.Simultaneously,H_(8)ETTB can passivate noncoord inated Pb^(2+)ions at the perovskite interface,promoting perovskite crystallization and reducing the interface energy barrier,resulting in a perovskite film with low defects and high crystalline quality.More importantly,the H_(8)ETTB molecule,can convert UV light into light absorbable by the perovskite,thereby reducing damage caused by UV light and improving the device's utilization of UV.Consequently,the champion PSC based on SnO_(2)-H_(8)ETTB achieves an impressing efficiency of 23.32%and significantly improved photostability compared with the control device after continuous exposure to intense UV radiation.In addition,the Cs_(0.05)(FA_(0.95)MA_(0.05))_(0.95)Pb(I_(0.95)Br_(0.05))_(3)based device can achieve maximum efficiency of 24.01%,demonstrating the effectiveness and universality of this strategy.Overall,this innovative interface bridging strategy effectively tackles interface defects and low UV light utilization in PSCs,presenting a promising approach for achieving highly efficient and stable PSCs.
基金National Key R&D Program of China(2021YFB3500400)National Natural Science Foundation of China(Grant No.12174152)+5 种基金Special Project of the Province-University Co-constructing Program of Jilin Province(SXGJXX2017-3)Jilin Province Natural Science Foundation of China(Nos.202513JC010277746 and 20190201307JC)Education Department of Jilin Province Project(JJKH20221004KJ)Interdisciplinary Integration and Innovation Project of JLU(JLUXKJC2021QZ14)China Postdoctoral Science Foundation(2021M701381)Jilin Province Science and Technology Innovation and Entrepreneurship Project for Overseas Students.
文摘Double perovskites(DPs)with Cs_(2)AgInCl_(6) composition,as one of the lead-free perovskites,have been in the spotlight owing to their intriguing optical properties,namely,self-trapped exciton(STE)emission and dopant-induced photoluminescence.However,the current DPs still face the challenge of low photoluminescence efficiency and cannot be applied in practice.Herein,we synthesize the Bi^(3+)and Eu^(3+)codoped Cs_(2)AgInCl_(6) DPs,which displays enhanced STE and Eu^(3+)ions characteristic emissions.Our results indicate that the Eu^(3+)ions mainly substitute the In sites and can increase the radiative recombination rate and exciton binding energy of STEs,which is discovered that Eu^(3+)ions can promote the localization of STEs by breaking the inversion symmetry of the Cs_(2)AgInCl_(6) lattice.The existence of Bi^(3+)ions decreases the excitation(absorption)energy,provides a new absorption channel,and increases the energy transfer rate to Eu^(3+)ions.Through adjusting the Bi^(3+)and Eu^(3+)concentrations,a maximum photoluminescence quantum yield of 80.1%is obtained in 6%Eu^(3+)and 0.5%Bi^(3+)codoped Cs_(2)AgInCl_(6) DPs.Finally,the high-quality single-component white-light-emitting diodes based on Bi^(3+)and Eu^(3+)codoped Cs_(2)AgInCl_(6) DPs and a 410-nm commercial ultraviolet chip are fabricated with the optimum color rendering index of 89,the optimal luminous efficiency of 88.1 lm/W,and a half-lifetime of 1,493 h.This work puts forward an effective lanthanide and transition metals codoping strategy to design single-component white-light emitter,taking a big step forward for the application lead-free DPs.
