The modification of the perovskite surface using functional additives is one of the most promising strategies to reduce nonradiative recombination and improve the stability of perovskite solar cells(PSCs).In this work...The modification of the perovskite surface using functional additives is one of the most promising strategies to reduce nonradiative recombination and improve the stability of perovskite solar cells(PSCs).In this work,a novel quaternary pyridinium-based halide salt,1-ethyl-4-(methoxycarbonyl)pyridinium iodide(EMCP-I),is introduced as an effective post-treatment molecule to improve the quality of the perovskite film.EMCP-I exhibits dual functionality to passivate both negatively and positively charged defects and improve the film morphology.Furthermore,the treatment fine-tunes energy level alignment between the perovskite layer and the hole transport layer(HTL),facilitating more efficient charge transport.Consequently,EMCP-I-treated devices achieve a remarkable power conversion efficiency(PCE)improvement from 20.5% to 22.6%,driven primarily by an enhanced open-circuit voltage(VOC).Beyond efficiency gains,the treatment significantly enhances the environmental and operational stabilities of solar cells.This work provides a guide for tailoring quaternary pyridinium-based molecules for simultaneous improvement of the efficiency and stability of PSCs.展开更多
The presence of SnZn-related defects in Cu_(2)ZnSn(S,Se)_(4)(CZTSSe)absorber results in large irreversible energy loss and extra irreversible electron-hole non-radiative recombination,thus hindering the efficiency enh...The presence of SnZn-related defects in Cu_(2)ZnSn(S,Se)_(4)(CZTSSe)absorber results in large irreversible energy loss and extra irreversible electron-hole non-radiative recombination,thus hindering the efficiency enhancement of CZTSSe devices.Although the incorporation of Ag in CZTSSe can effectively suppress the SnZn-related defects and significantly improve the resulting cell performance,an excellent efficiency has not been achieved to date primarily owing to the poor electrical-conductivity and the low carrier density of the CZTSSe film induced by Ag substitution.Herein,this study exquisitely devises an Ag/H co-doping strategy in CZTSSe absorber via Ag substitution programs followed by hydrogen-plasma treatment procedure to suppress SnZn defects for achieving efficient CZTSSe devices.In-depth investigation results demonstrate that the incorporation of H in Ag-based CZTSSe absorber is expected to improve the poor electrical-conductivity and the low carrier density caused by Ag substitution.Importantly,the C=O and O-H functional groups induced by hydrogen incorporation,serving as an electron donor,can interact with under-coordinated cations in CZTSSe material,effectively passivating the SnZn-related defects.Consequently,the incorporation of an appropriate amount of Ag/H in CZTSSe mitigates carrier non-radiative recombination,prolongs minority carrier lifetime,and thus yields a champion efficiency of 14.74%,showing its promising application in kesterite-based CZTSSe devices.展开更多
The advantages of the Ge–Pb-based perovskite solar cells(PSCs),such as low bandgap,have made this kind of PSC popular nowadays.Nevertheless,they have adverse properties that need to be fixed,such as short lifetime an...The advantages of the Ge–Pb-based perovskite solar cells(PSCs),such as low bandgap,have made this kind of PSC popular nowadays.Nevertheless,they have adverse properties that need to be fixed,such as short lifetime and fast crystallization process,which causes Ge defects.In this research,the passivation of Ge defects by using pyridinium chlorochromate methylamine iodine(PCCMAI)in the perovskite film(PF)structure is investigated.By using PCCMAI,the PSC's performance enhancement and surface morphology optimization were observed.展开更多
All-inorganic halide perovskite solar cells(PSCs)have acquired great progress,especially CsPbI2Br.However,their photoelectric conversion efficiency(PCE)remains far below the theoretical predictions.Non-radiative recom...All-inorganic halide perovskite solar cells(PSCs)have acquired great progress,especially CsPbI2Br.However,their photoelectric conversion efficiency(PCE)remains far below the theoretical predictions.Non-radiative recombination is one of the important issues affecting the photoelectric performance of the PSCs,and the defective lead ions derived from the evaporation of halide ions in the inorganic perovskite are the principal non-radiative recombination centers.Herein,the non-radiative recombination is effectively suppressed by introducing the N-methyl-2-pyrrolidone(NMP)as a Lewis base molecule to passivate the defective lead ions.Therefore,by adjusting the dosage of NMP,the smooth and pinhole-free CsPbI_(2)Br perovskite film is obtained and the optimized device exhibits a champion PCE of 16.77%with an excellent fill factor(FF)of 0.80.This work proves the effectiveness of passivation using Lewis base molecules to prevent non-radiative recombination defects in inorganic perovskite.展开更多
Defect passivation is one of the most important strategies to boost both the efficiency and stability of perovskite solar cells(PSCs).Here,nontoxic and sustainable forest-based biomaterial,betulin,is first introduced ...Defect passivation is one of the most important strategies to boost both the efficiency and stability of perovskite solar cells(PSCs).Here,nontoxic and sustainable forest-based biomaterial,betulin,is first introduced into perovskites.The experiments and calculations reveal that betulin can effectively passivate the uncoordinated lead ions in perovskites via sharing the lone pair electrons of hydroxyl group,promoting charge transport.As a result,the power conversion efficiencies of the p-i-n planar PSCs remarkably increase from 19.14%to 21.15%,with the improvement of other parameters.The hydrogen bonds of betulin lock methylamine and halogen ions along the grain boundaries and on the film surface and thus suppress ion migration,further stabilizing perovskite crystal structures.These positive effects enable the PSCs to maintain 90%of the initial efficiency after 30 days in ambient air with 60%±5%relative humidity,75%after 300 h aging at 85℃,and 55%after 250 h light soaking,respectively.This work opens a new pathway for using nontoxic and low-cost biomaterials from forest to make highly efficient and stable PSCs.展开更多
The grain surfaces(film surface and grain boundary)of polycrystalline perovskite films are vulnerable sites in solar cells since they pose a high defect density and initiate the degradation of perovskite absorber.Achi...The grain surfaces(film surface and grain boundary)of polycrystalline perovskite films are vulnerable sites in solar cells since they pose a high defect density and initiate the degradation of perovskite absorber.Achieving simultaneously defect passivation and grain protection from moisture is crucial for the viability of perovskite solar cells.Here,an in situ cross-linked grain encapsulation(CLGE)strategy that improves both device stability and defect passivation is reported.Cross-linkable semiconducting small molecules are mixed into the antisolvent to uniformly form a compact and conducting cross-linked layer over the grain surfaces.This cross-linked coating layer not only passivates trap states and facilitates hole extraction,but also enhances the device stability by preventing moisture diffusion.Using the CLGE strategy,a high power conversion efficiency(PCE)of 22.7%is obtained in 1.55-eV bandgap planar perovskite solar cells.The unencapsulated devices with CLGE exhibit significantly enhanced device stability again moisture and maintain>90%of their initial PCE after shelf storage under ambient condition for over10,000 h.展开更多
Defects as non-radiative recombination centers hinder the further efficiency improvements of perovskite solar cells(PSCs).Additive engineering has been demonstrated to be an effective method for defect passivation in ...Defects as non-radiative recombination centers hinder the further efficiency improvements of perovskite solar cells(PSCs).Additive engineering has been demonstrated to be an effective method for defect passivation in perovskite films.Here,we employed(4-methoxyphenyl)potassium trifluoroborate(C_(7)H_(7)BF_(3)KO)with and K+functional groups to passivate spray-coated(FAPbI_(3))_(x)(MAPbBr_(3))_(1-x) perovskite and eliminate hysteresis.It is shown that the F of can form hydrogen bonds with the H atom in the amino group of MA+/FA+ions of perovskite,thus reducing the generation of MA+/FA+vacancies and improving device efficiency.Meanwhile,K+and reduced MA+/FA+vacancies can inhibit ion migration,thereby eliminating hysteresis.With the aid of C_(7)H_(7)BF_(3)KO,we obtained hysteresis-free PSCs with the maximum efficiency of 19.5%by spray-coating in air.Our work demonstrates that additive engineering is promising to improve the performance of spray-coated PSCs.展开更多
The light weight,good bending resistance and low production cost make flexible perovskite solar cells(PSCs)good candidates in wearable electronics,portable charger,remote power,and flying objects.High power conversion...The light weight,good bending resistance and low production cost make flexible perovskite solar cells(PSCs)good candidates in wearable electronics,portable charger,remote power,and flying objects.High power conversion efficiency(PCE)plays a crucial role on obtaining the high mass specific power of flexible devices.However,the performance for flexible PSCs is still having a large room to be improved.Here,we added the 2-amino-5-cyanopyridine(ACP)molecule with a polar electron density distribution in the perovskite precursor solution to improve the performance of flexible PSCs.The cyano groups with electron-withdrawing ability are expected to passivate positively charged point defects,while amines with electron donating ability are expected to passivate negatively charged point defects in perovskite films.Thanks to the effective passivation of defects at the grain boundary and surface of perovskite films,the PCE of flexible PSCs is obviously increased from 16.9%to 18.0%.These results provide a universal approach to improve performance of flexible PSCs by healing the defects in perovskite films through electrostatic interactions.展开更多
Rational interface engineering is essential for minimizing interfacial nonradiative recombination losses and enhancing device performance.Herein,we report the use of bidentate diphenoxybenzene(DPOB)isomers as surface ...Rational interface engineering is essential for minimizing interfacial nonradiative recombination losses and enhancing device performance.Herein,we report the use of bidentate diphenoxybenzene(DPOB)isomers as surface modifiers for perovskite films.The DPOB molecules,which contain two oxygen(O)atoms,chemically bond with undercoordinated Pb^(2+) on the surface of perovskite films,resulting in compression of the perovskite lattice.This chemical interaction,along with physical regulations,leads to the formation of high-quality perovskite films with compressive strain and fewer defects.This compressive strain-induced band bending promotes hole extraction and transport,while inhibiting charge recombination at the interfaces.Furthermore,the addition of DPOB will reduce the zero-dimensional(OD) Cs_4PbBr_6 phase and produce the two-dimensional(2D) CsPb_(2)Br_5 phase,which is also conducive to the improvement of device performance.Ultimately,the resulting perovskite films,which are strain-released and defect-passivated,exhibit exceptional device efficiency,reaching 10.87% for carbon-based CsPbBr_(3) device,14.86% for carbon-based CsPbI_(2)Br device,22,02% for FA_(0.97)Cs_(0.03)PbI_(3) device,respectively.Moreover,the unencapsulated CsPbBr_(3) PSC exhibits excellent stability under persistent exposure to humidity(80%) and heat(80℃) for over 50 days.展开更多
Inverted perovskite solar cells have gained prominence in industrial advancement due to their easy fabrication,low hysteresis effects,and high stability.Despite these advantages,their efficiency is currently limited b...Inverted perovskite solar cells have gained prominence in industrial advancement due to their easy fabrication,low hysteresis effects,and high stability.Despite these advantages,their efficiency is currently limited by excessive defects and poor carrier transport at the perovskite-electrode interface,particularly at the buried interface between the perovskite and transparent conductive oxide(TCO).Recent efforts in the perovskite community have focused on designing novel self-assembled molecules(SAMs)to improve the quality of the buried interface.However,a notable gap remains in understanding the regulation of atomic-scale interfacial properties of SAMs between the perovskite and TCO interfaces.This understanding is crucial,particularly in terms of identifying chemically active anchoring groups.In this study,we used the star SAM([2-(9H-carbazol-9-yl)ethyl]phosphonic acid)as the base structure to investigate the defect passivation effects of eight common anchoring groups at the perovskite-TCO interface.Our findings indicate that the phosphonic and boric acid groups exhibit notable advantages.These groups fulfill three key criteria:they provide the greatest potential for defect passivation,exhibit stable adsorption with defects,and exert significant regulatory effects on interface dipoles.Ionized anchoring groups exhibit enhanced passivation capabilities for defect energy levels due to their superior Lewis base properties,which effectively neutralize local charges near defects.Among various defect types,iodine vacancies are the easiest to passivate,whereas iodine-substituted lead defects are the most challenging to passivate.Our study provides comprehensive theoretical insights and inspiration for the design of anchoring groups in SAMs,contributing to the ongoing development of more efficient inverted perovskite solar cells.展开更多
The buried interface defects severely affect the further enhancements of efficiency and stability of SnO_(2)-based planar perovskite solar cells(PSCs).To well tackle this problem,we propose a passivation strategy empl...The buried interface defects severely affect the further enhancements of efficiency and stability of SnO_(2)-based planar perovskite solar cells(PSCs).To well tackle this problem,we propose a passivation strategy employing NH_(4)PF_6 to modify the buried interface of perovskite layer((FAPbI_(3))_(0.85)(MAPbBr_(3))_(0.15) composition) in planar PSCs.After introducing NH_(4)PF_(6),the oxygen defects on the surface of SnO_(2) film are greatly restricted due to the coordinate interaction between fluorine atoms(F) in PF_(6)^(-)and undercoordinated Sn^(4+).Meanwhile,the hydrogen bonding interaction(N-H…I) between NH_(4)PF_(6) and PbI_(2) can passivate the non-radiative charge recombination sites,significantly optimizing the quality of perovskite film,as well as the charge transfer process at the SnO_(2)/perovskite interface.As a result,the NH_(4)PF_(6)-modified PSC obtains a champion power conversion efficiency(PCE) of 21.11%superior to the reference device(18.46%),and the device with an active area of 1 cm^(2) achieves a PCE as high as17.38%.Furthermore,the unencapsulated NH_(4)PF_(6)-modified PSCs show good humidity stability and retain about80% of the initial PCE after 1080 h aging at the relative humidity(RH) of 35% ± 5%.展开更多
Although ionic liquids(ILs)have been widely employed to heal the defects in perovskite solar cells(PSCs),the corresponding defect passivation mechanisms are not thoroughly understood up to now.Herein,we first reveal a...Although ionic liquids(ILs)have been widely employed to heal the defects in perovskite solar cells(PSCs),the corresponding defect passivation mechanisms are not thoroughly understood up to now.Herein,we first reveal an abnormal buried interface anion defect passivation mechanism depending on cationinduced steric hindrance.The IL molecules containing the same anion([BF4]^(-))and different sizes of imidazolium cations induced by substituent size are used to manipulate buried interface.It was revealed what passivated interfacial defects is mainly anions instead of cations.Theoretical and experimental results demonstrate that the large-sized cations can weaken the ionic bond strength between anions and cations,and facilitate the interaction between anions and SnO2as well as perovskites,which is conducive to interfacial defect passivation and ameliorating interfacial contact.It can be concluded that interfacial chemical interaction strength and defect passivation effect are positively correlated with the size of cations.The discovery breaks conventional thinking that large-sized modification molecules would weaken their chemical interaction with perovskite.Compared with the control device(21.54%),the device based on 1,3-Bis(1-adamantyl)-imidazolium tetrafluoroborate(BAIMBF4)with maximum size cations achieves a significantly enhanced efficiency of 23.61%along with much increased moisture,thermal and light stabilities.展开更多
Metal halide perovskites,particularly the quasi-two-dimensional perovskite subclass,have exhibited considerable potential for next-generation electroluminescent materials for lighting and display.Nevertheless,the pres...Metal halide perovskites,particularly the quasi-two-dimensional perovskite subclass,have exhibited considerable potential for next-generation electroluminescent materials for lighting and display.Nevertheless,the presence of defects within these perovskites has a substantial influence on the emission efficiency and durability of the devices.In this study,we revealed a synergistic passivation mechanism on perovskite films by using a dual-functional compound of potassium bromide.The dual functional potassium bromide on the one hand can passivate the defects of halide vacancies with bromine anions and,on the other hand,can screen the charged defects at the grain boundaries with potassium cations.This approach effectively reduces the probability of carriers quenching resulting from charged defects capture and consequently enhances the radiative recombination efficiency of perovskite thin films,leading to a significant enhancement of photoluminescence quantum yield to near-unity values(95%).Meanwhile,the potassium bromide treatment promoted the growth of homogeneous and smooth film,facilitating the charge carrier injection in the devices.Consequently,the perovskite light-emitting diodes based on this strategy achieve a maximum external quantum efficiency of~21%and maximum luminance of~60,000 cd m^(-2).This work provides a deeper insight into the passivation mechanism of ionic compound additives in perovskite with the solution method.展开更多
The non-radiative loss in a perovskite,mainly resulting from thermal defects and halogen vacancies,has always been an important factor affecting its luminescence properties.The addition of a lithium ion has been demon...The non-radiative loss in a perovskite,mainly resulting from thermal defects and halogen vacancies,has always been an important factor affecting its luminescence properties.The addition of a lithium ion has been demonstrated to be an effective way to reduce the nonradiative recombination in perovskitefilms,mainly acting on the surface/interface of thefilms.However,few studies have focused on its role in col loidal quantum dots.Herein,we have used LiBr as a new dual-defect passivation agent in colloidal CsPbX_(3)(X=Br andⅠ)quantum dots to reduce the capture ability of the defects for excited electrons,leading to an effective reduction of the non-radiative recombination.The mechanism of LiBr doping in CsPbX_(3)(X=Br andⅠ)quantum dots was studied by exploring its photodynamic process at room temperature and low temperature.Our results show that an appropriate concentration of LiBr can not only passivate the halide vacancy and thermal defect to reduce the nonradiative recombination,but also improve the phase stabi lity caused by halide migration.展开更多
Correction for‘The dual-defect passivation role of lithium bromide doping in reducing the nonradiative loss in CsPbX_(3)(X=Br and I)quantum dots’by Hao Wu et al.,Inorg.Chem.Front.,2020,DOI:10.1039/d0qi01262a.
Lead-iodine perovskites are emerging as promising candidates for next-generation solar cells,yet a divergence persists between the theoretical and experimental realms regarding the impact of surface iodine vacancies(V...Lead-iodine perovskites are emerging as promising candidates for next-generation solar cells,yet a divergence persists between the theoretical and experimental realms regarding the impact of surface iodine vacancies(V_(I))on device performance.To elevate cell efficiency,a profound understanding and delicate control of V_(I) and their passivation mechanisms are crucial.In this work,we studied various V_(I) defects near the surface of all-inorganic CsPbI3 perovskite using ab initio non-adiabatic molecular dynamics.The results show that the electron-hole(e-h)recombination lifetime highly depends on the defect positions and configurations,as well as the efficacy of Lewis base additives in passivating defects.Despite the outermost layer V_(I) creating no defect state within the band gap,the carrier recombination rate accelerates significantly by a factor of 2 compared to that with the defect-free surface,owing to strong electron-phonon coupling.Subsurface defects create a localized hole trapping state,enabling swift capture of valence band holes,which subsequently accelerate recombination with the conduction band electrons by a factor of 6.5.Remarkably for Pb-dimers,this rate escalates 13-fold.Incorporating the Lewis base molecule HCOO-forms the stable Pb-O bonds with lead ions,preventing surface V_(I) reconstruction(iodine migration),Pb-dimer formation,and an in-band defect state.These effectively reduce the electron-phonon coupling,achieving performance comparable to that of the defect-free surface.This work reconciles contradictory of surface V_(I) on perovskite performance,and enriches our understanding of surface defect properties and their effects on carrier dynamics and device efficiency.展开更多
Cesium lead iodide perovskites offer promising stability and a bandgap near 1.7 eV,making them suitable as the top cell in tandem solar cells.However,the inorganic perovskite films suffer from a high defect density an...Cesium lead iodide perovskites offer promising stability and a bandgap near 1.7 eV,making them suitable as the top cell in tandem solar cells.However,the inorganic perovskite films suffer from a high defect density and substantial recombination losses,undermining their optoelectronic performances.Here,by activating the aromatic system,we develop 4-methoxybenzoylhydrazine(MeOBH)-modified CsPbI_(3) film with regulated crystallinity,suppressed non-radiative recombination,and improved interfacial energetic alignment.The resultant inorganic perovskite solar cells achieved a power conversion efficiency of 20.95%,along with enhanced phase stability owing to the strong coordination interaction between the lead cation and the hydrazide group.Encapsulated devices retain 90.4% of the initial performance after 624 h of maximum power point operation under the ISOS-L-1I protocol.展开更多
Defects at the grain boundaries(GBs)of perovskite film highly restrict both the efficiency and stability of perovskite solar cells(PSCs).Herein,organic small molecules of butanedioic acid(BA)and acetylenedicarboxylic ...Defects at the grain boundaries(GBs)of perovskite film highly restrict both the efficiency and stability of perovskite solar cells(PSCs).Herein,organic small molecules of butanedioic acid(BA)and acetylenedicarboxylic acid(AA),containing two carbonyl(C=O)groups and different core-units,were incorporated into perovskite as additives for PSCs application.Thanks to the strong coordination interaction between C=O group and under-coordinated Pb^(2+),the additives can effectively passivate film defects and regulate the perovskite crystallization,yielding high-quality perovskite films with lower defect densities.More importantly,the additives can efficiently regulate the charge transport behaviors in PSCs.Benefiting from the defects passivation and the regulation of charge carrier dynamics,the BA and AA-treaded PSCs show the power conversion efficiencies of 21.52%and 20.50%,which are higher than that of the control device(19.41%).Besides,the optimal devices exhibit a remarkable enhanced long-term stability and moisture tolerance compared to the pristine devices.Furthermore,the transient absorption spectrum reveals the mechanism of enhanced photovoltaic performances,attributing to the improvement of charge transport capability at the perovskite/Spiro-OMeTAD interfaces.This work affords a promising strategy to improve the efficiency and stability of PSCs through regulating the charge-carrier dynamic process in perovskite film.展开更多
Bulk and interface carrier nonradiative recombination losses impede the further improvement of power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs).It is highly necessary to develop multifunct...Bulk and interface carrier nonradiative recombination losses impede the further improvement of power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs).It is highly necessary to develop multifunctional strategy to minimize surface and interface nonradiative recombination losses.Herein,we report a bulk and interface defect passivation strategy via the synergistic effect of anions and cations,where multifunctional potassium sulphate(K_(2)SO_(4))is incorporated at SnO_(2)/perovskite interface.We find that K^(+)ions in K_(2)SO_(4)diffuse into perovskite layer and suppress the formation of bulk defects in perovskite films,and the SO_(4)^(2-)ions remain located at interface via the strong chemical interaction with SnO_(2)layer and perovskite layer,respectively.Through this synergistic modification strategy,effective defect passivation and improved energy band alignment are achieved simultaneously.These beneficial effects are translated into an efficiency increase from 19.45%to 21.18%with a low voltage deficit of0.53 V mainly as a result of boosted open-circuit voltage(V_(oc))after K_(2)SO_(4)modification.In addition,the K_(2)SO_(4)modification contributes to ameliorated stability.The present work provides a route to minimize bulk and interface nonradiative recombination losses for the simultaneous realization of PCE and stability enhancement by rational anion and cation synergistic engineering.展开更多
Surface and grain boundary defects in halide perovskite solar cells are highly detrimental,reducing efficiencies and stabilities.Widespread halide anion and organic cation defects usually aggravate ion diffusion and m...Surface and grain boundary defects in halide perovskite solar cells are highly detrimental,reducing efficiencies and stabilities.Widespread halide anion and organic cation defects usually aggravate ion diffusion and material degradation on the surfaces and at the grain boundaries of perovskite films.In this study,we employ an in-situ green method utilizing nontoxic cetyltrimethylammonium chloride(CTAC)and isopropanol(IPA)as anti-solvents to effectively passivate both surface and grain boundary defects in hybrid perovskites.Anion vacancies can be readily passivated by the chloride group due to its high electronegativity,and cation defects can be synchronously passivated by the more stable cetyltrimethylammonium group.The results show that the charge trap density was significantly reduced,while the carrier recombination lifetime was markedly extended.As a result,the power conversion efficiency of the cell can reach 23.4%with this in-situ green method.In addition,the device retains 85%of its original power conversion efficiency after 600 h of operation under illumination,showing that the stability of perovskite solar cells is improved with this in-situ passivation strategy.This work may provide a green and effective route to improve both the stability and efficiency of perovskite solar cells.展开更多
基金financially supported by The Scientific and Technological Research Council of Türkiye(TüBITAK)under Project No.119F185the support of the Interdisciplinary Centre for Mathematical and Computational Modelling at the University of Warsaw(ICM UW)under computational allocation no.g93-1617。
文摘The modification of the perovskite surface using functional additives is one of the most promising strategies to reduce nonradiative recombination and improve the stability of perovskite solar cells(PSCs).In this work,a novel quaternary pyridinium-based halide salt,1-ethyl-4-(methoxycarbonyl)pyridinium iodide(EMCP-I),is introduced as an effective post-treatment molecule to improve the quality of the perovskite film.EMCP-I exhibits dual functionality to passivate both negatively and positively charged defects and improve the film morphology.Furthermore,the treatment fine-tunes energy level alignment between the perovskite layer and the hole transport layer(HTL),facilitating more efficient charge transport.Consequently,EMCP-I-treated devices achieve a remarkable power conversion efficiency(PCE)improvement from 20.5% to 22.6%,driven primarily by an enhanced open-circuit voltage(VOC).Beyond efficiency gains,the treatment significantly enhances the environmental and operational stabilities of solar cells.This work provides a guide for tailoring quaternary pyridinium-based molecules for simultaneous improvement of the efficiency and stability of PSCs.
基金supported by the National Natural Science Foundation of China(51802081,62074052,and 62104061)the Natural Science Foundation of Henan Province(232300420145).
文摘The presence of SnZn-related defects in Cu_(2)ZnSn(S,Se)_(4)(CZTSSe)absorber results in large irreversible energy loss and extra irreversible electron-hole non-radiative recombination,thus hindering the efficiency enhancement of CZTSSe devices.Although the incorporation of Ag in CZTSSe can effectively suppress the SnZn-related defects and significantly improve the resulting cell performance,an excellent efficiency has not been achieved to date primarily owing to the poor electrical-conductivity and the low carrier density of the CZTSSe film induced by Ag substitution.Herein,this study exquisitely devises an Ag/H co-doping strategy in CZTSSe absorber via Ag substitution programs followed by hydrogen-plasma treatment procedure to suppress SnZn defects for achieving efficient CZTSSe devices.In-depth investigation results demonstrate that the incorporation of H in Ag-based CZTSSe absorber is expected to improve the poor electrical-conductivity and the low carrier density caused by Ag substitution.Importantly,the C=O and O-H functional groups induced by hydrogen incorporation,serving as an electron donor,can interact with under-coordinated cations in CZTSSe material,effectively passivating the SnZn-related defects.Consequently,the incorporation of an appropriate amount of Ag/H in CZTSSe mitigates carrier non-radiative recombination,prolongs minority carrier lifetime,and thus yields a champion efficiency of 14.74%,showing its promising application in kesterite-based CZTSSe devices.
基金support(Research University Excel ence Initiative)through Silesian University of Technology grant No.32/014/SDU/10-22-78。
文摘The advantages of the Ge–Pb-based perovskite solar cells(PSCs),such as low bandgap,have made this kind of PSC popular nowadays.Nevertheless,they have adverse properties that need to be fixed,such as short lifetime and fast crystallization process,which causes Ge defects.In this research,the passivation of Ge defects by using pyridinium chlorochromate methylamine iodine(PCCMAI)in the perovskite film(PF)structure is investigated.By using PCCMAI,the PSC's performance enhancement and surface morphology optimization were observed.
基金supported by the National Key R&D Program of China(2016YFB0303602)Sichuan and Technology Program(Grant No.2018JY0015)Yong Science and Technology Innovation Team Project of SWPU(No.2019CXTD04)。
文摘All-inorganic halide perovskite solar cells(PSCs)have acquired great progress,especially CsPbI2Br.However,their photoelectric conversion efficiency(PCE)remains far below the theoretical predictions.Non-radiative recombination is one of the important issues affecting the photoelectric performance of the PSCs,and the defective lead ions derived from the evaporation of halide ions in the inorganic perovskite are the principal non-radiative recombination centers.Herein,the non-radiative recombination is effectively suppressed by introducing the N-methyl-2-pyrrolidone(NMP)as a Lewis base molecule to passivate the defective lead ions.Therefore,by adjusting the dosage of NMP,the smooth and pinhole-free CsPbI_(2)Br perovskite film is obtained and the optimized device exhibits a champion PCE of 16.77%with an excellent fill factor(FF)of 0.80.This work proves the effectiveness of passivation using Lewis base molecules to prevent non-radiative recombination defects in inorganic perovskite.
基金supported by the National Natural Science Foundation of China(21875067,51811530011,11604099)the Fundamental Research Funds for the Central Universities,Shanghai Rising-Star(19QA1403100)+2 种基金ECNU Multifunctional Platform for Innovation(006)the National Key Research and Development Program of China(2017YFA0206600)the National Natural Science Foundation of China(51773045,21772030,51922032,21961160720)for financial support。
文摘Defect passivation is one of the most important strategies to boost both the efficiency and stability of perovskite solar cells(PSCs).Here,nontoxic and sustainable forest-based biomaterial,betulin,is first introduced into perovskites.The experiments and calculations reveal that betulin can effectively passivate the uncoordinated lead ions in perovskites via sharing the lone pair electrons of hydroxyl group,promoting charge transport.As a result,the power conversion efficiencies of the p-i-n planar PSCs remarkably increase from 19.14%to 21.15%,with the improvement of other parameters.The hydrogen bonds of betulin lock methylamine and halogen ions along the grain boundaries and on the film surface and thus suppress ion migration,further stabilizing perovskite crystal structures.These positive effects enable the PSCs to maintain 90%of the initial efficiency after 30 days in ambient air with 60%±5%relative humidity,75%after 300 h aging at 85℃,and 55%after 250 h light soaking,respectively.This work opens a new pathway for using nontoxic and low-cost biomaterials from forest to make highly efficient and stable PSCs.
基金financially supported by the National Key R&D Program of China(2018YFB1500102,2018YFB2200101)the National Natural Science Foundation of China(61974063,61921005)+3 种基金Natural Science Foundation of Jiangsu Province(BK20190315)the Fundamental Research Funds for the Central Universities(14380168)the Thousand Talent Program for Young Outstanding Scientists in ChinaProgram for Innovative Talents and Entrepreneur in Jiangsu。
文摘The grain surfaces(film surface and grain boundary)of polycrystalline perovskite films are vulnerable sites in solar cells since they pose a high defect density and initiate the degradation of perovskite absorber.Achieving simultaneously defect passivation and grain protection from moisture is crucial for the viability of perovskite solar cells.Here,an in situ cross-linked grain encapsulation(CLGE)strategy that improves both device stability and defect passivation is reported.Cross-linkable semiconducting small molecules are mixed into the antisolvent to uniformly form a compact and conducting cross-linked layer over the grain surfaces.This cross-linked coating layer not only passivates trap states and facilitates hole extraction,but also enhances the device stability by preventing moisture diffusion.Using the CLGE strategy,a high power conversion efficiency(PCE)of 22.7%is obtained in 1.55-eV bandgap planar perovskite solar cells.The unencapsulated devices with CLGE exhibit significantly enhanced device stability again moisture and maintain>90%of their initial PCE after shelf storage under ambient condition for over10,000 h.
基金the National Natural Science Foundation of China(51861145101).
文摘Defects as non-radiative recombination centers hinder the further efficiency improvements of perovskite solar cells(PSCs).Additive engineering has been demonstrated to be an effective method for defect passivation in perovskite films.Here,we employed(4-methoxyphenyl)potassium trifluoroborate(C_(7)H_(7)BF_(3)KO)with and K+functional groups to passivate spray-coated(FAPbI_(3))_(x)(MAPbBr_(3))_(1-x) perovskite and eliminate hysteresis.It is shown that the F of can form hydrogen bonds with the H atom in the amino group of MA+/FA+ions of perovskite,thus reducing the generation of MA+/FA+vacancies and improving device efficiency.Meanwhile,K+and reduced MA+/FA+vacancies can inhibit ion migration,thereby eliminating hysteresis.With the aid of C_(7)H_(7)BF_(3)KO,we obtained hysteresis-free PSCs with the maximum efficiency of 19.5%by spray-coating in air.Our work demonstrates that additive engineering is promising to improve the performance of spray-coated PSCs.
基金financial support from the National Natural Science Foundation of China(No.NSFC21773218)。
文摘The light weight,good bending resistance and low production cost make flexible perovskite solar cells(PSCs)good candidates in wearable electronics,portable charger,remote power,and flying objects.High power conversion efficiency(PCE)plays a crucial role on obtaining the high mass specific power of flexible devices.However,the performance for flexible PSCs is still having a large room to be improved.Here,we added the 2-amino-5-cyanopyridine(ACP)molecule with a polar electron density distribution in the perovskite precursor solution to improve the performance of flexible PSCs.The cyano groups with electron-withdrawing ability are expected to passivate positively charged point defects,while amines with electron donating ability are expected to passivate negatively charged point defects in perovskite films.Thanks to the effective passivation of defects at the grain boundary and surface of perovskite films,the PCE of flexible PSCs is obviously increased from 16.9%to 18.0%.These results provide a universal approach to improve performance of flexible PSCs by healing the defects in perovskite films through electrostatic interactions.
基金National Natural Science Foundation of China (62104136, 22179051, 62204098, 52104258)Project of Shandong Province Higher Educational Young Innovative Team (2022KJ218)+3 种基金China Postdoctoral Science Foundation (2023M732104)Qingdao Postdoctoral Funding Program (QDBSH20220201002)Postdoctoral Innovation Project of Shandong Province (SDCX-ZG-202303032)Shandong Provincial Natural Science Foundation (ZR2021ME016)。
文摘Rational interface engineering is essential for minimizing interfacial nonradiative recombination losses and enhancing device performance.Herein,we report the use of bidentate diphenoxybenzene(DPOB)isomers as surface modifiers for perovskite films.The DPOB molecules,which contain two oxygen(O)atoms,chemically bond with undercoordinated Pb^(2+) on the surface of perovskite films,resulting in compression of the perovskite lattice.This chemical interaction,along with physical regulations,leads to the formation of high-quality perovskite films with compressive strain and fewer defects.This compressive strain-induced band bending promotes hole extraction and transport,while inhibiting charge recombination at the interfaces.Furthermore,the addition of DPOB will reduce the zero-dimensional(OD) Cs_4PbBr_6 phase and produce the two-dimensional(2D) CsPb_(2)Br_5 phase,which is also conducive to the improvement of device performance.Ultimately,the resulting perovskite films,which are strain-released and defect-passivated,exhibit exceptional device efficiency,reaching 10.87% for carbon-based CsPbBr_(3) device,14.86% for carbon-based CsPbI_(2)Br device,22,02% for FA_(0.97)Cs_(0.03)PbI_(3) device,respectively.Moreover,the unencapsulated CsPbBr_(3) PSC exhibits excellent stability under persistent exposure to humidity(80%) and heat(80℃) for over 50 days.
基金supported by the National Natural Science Foundation of China(Grant Nos.62321166653,22090044,and 12350410372).Calculations were performed in part at the high-performance computing center of Jilin University.
文摘Inverted perovskite solar cells have gained prominence in industrial advancement due to their easy fabrication,low hysteresis effects,and high stability.Despite these advantages,their efficiency is currently limited by excessive defects and poor carrier transport at the perovskite-electrode interface,particularly at the buried interface between the perovskite and transparent conductive oxide(TCO).Recent efforts in the perovskite community have focused on designing novel self-assembled molecules(SAMs)to improve the quality of the buried interface.However,a notable gap remains in understanding the regulation of atomic-scale interfacial properties of SAMs between the perovskite and TCO interfaces.This understanding is crucial,particularly in terms of identifying chemically active anchoring groups.In this study,we used the star SAM([2-(9H-carbazol-9-yl)ethyl]phosphonic acid)as the base structure to investigate the defect passivation effects of eight common anchoring groups at the perovskite-TCO interface.Our findings indicate that the phosphonic and boric acid groups exhibit notable advantages.These groups fulfill three key criteria:they provide the greatest potential for defect passivation,exhibit stable adsorption with defects,and exert significant regulatory effects on interface dipoles.Ionized anchoring groups exhibit enhanced passivation capabilities for defect energy levels due to their superior Lewis base properties,which effectively neutralize local charges near defects.Among various defect types,iodine vacancies are the easiest to passivate,whereas iodine-substituted lead defects are the most challenging to passivate.Our study provides comprehensive theoretical insights and inspiration for the design of anchoring groups in SAMs,contributing to the ongoing development of more efficient inverted perovskite solar cells.
基金financially supported by the National Natural Science Foundation of China (Nos. 22179053, 22279046 and 21905119)the Natural Science Excellent Youth Foundation of Jiangsu Provincial (No. BK20220112)the Six-Peak Top Talents in Jiangsu province (No. XNY066)。
文摘The buried interface defects severely affect the further enhancements of efficiency and stability of SnO_(2)-based planar perovskite solar cells(PSCs).To well tackle this problem,we propose a passivation strategy employing NH_(4)PF_6 to modify the buried interface of perovskite layer((FAPbI_(3))_(0.85)(MAPbBr_(3))_(0.15) composition) in planar PSCs.After introducing NH_(4)PF_(6),the oxygen defects on the surface of SnO_(2) film are greatly restricted due to the coordinate interaction between fluorine atoms(F) in PF_(6)^(-)and undercoordinated Sn^(4+).Meanwhile,the hydrogen bonding interaction(N-H…I) between NH_(4)PF_(6) and PbI_(2) can passivate the non-radiative charge recombination sites,significantly optimizing the quality of perovskite film,as well as the charge transfer process at the SnO_(2)/perovskite interface.As a result,the NH_(4)PF_(6)-modified PSC obtains a champion power conversion efficiency(PCE) of 21.11%superior to the reference device(18.46%),and the device with an active area of 1 cm^(2) achieves a PCE as high as17.38%.Furthermore,the unencapsulated NH_(4)PF_(6)-modified PSCs show good humidity stability and retain about80% of the initial PCE after 1080 h aging at the relative humidity(RH) of 35% ± 5%.
基金financially supported by the Support Plan for Overseas Students to Return to China for Entrepreneurship and Innovation(cx2020003)the Fundamental Research Funds for the Central Universities(2020CDJ-LHZZ-074 and 2021CDJQY-022)Natural Science Foundation of Chongqing(cstc2020jcyjmsxmX0629)。
文摘Although ionic liquids(ILs)have been widely employed to heal the defects in perovskite solar cells(PSCs),the corresponding defect passivation mechanisms are not thoroughly understood up to now.Herein,we first reveal an abnormal buried interface anion defect passivation mechanism depending on cationinduced steric hindrance.The IL molecules containing the same anion([BF4]^(-))and different sizes of imidazolium cations induced by substituent size are used to manipulate buried interface.It was revealed what passivated interfacial defects is mainly anions instead of cations.Theoretical and experimental results demonstrate that the large-sized cations can weaken the ionic bond strength between anions and cations,and facilitate the interaction between anions and SnO2as well as perovskites,which is conducive to interfacial defect passivation and ameliorating interfacial contact.It can be concluded that interfacial chemical interaction strength and defect passivation effect are positively correlated with the size of cations.The discovery breaks conventional thinking that large-sized modification molecules would weaken their chemical interaction with perovskite.Compared with the control device(21.54%),the device based on 1,3-Bis(1-adamantyl)-imidazolium tetrafluoroborate(BAIMBF4)with maximum size cations achieves a significantly enhanced efficiency of 23.61%along with much increased moisture,thermal and light stabilities.
基金supported by the Science and Technology Development Fund,Macao SAR(File no.FDCT-0082/2021/A2,0010/2022/AMJ,006/2022/ALC)UM's research fund(File no.MYRG2022-00241-IAPME,MYRGCRG2022-00009-FHS)+2 种基金the research fund from Wuyi University(EF38/IAPME-XGC/2022/WYU)the Natural Science Foundation of China(61935017,62175268)Science,Technology and Innovation Commission of Shenzhen Municipality(Project Nos.JCYJ20220530113015035,JCYJ20210324120204011,and KQTD2015071710313656).
文摘Metal halide perovskites,particularly the quasi-two-dimensional perovskite subclass,have exhibited considerable potential for next-generation electroluminescent materials for lighting and display.Nevertheless,the presence of defects within these perovskites has a substantial influence on the emission efficiency and durability of the devices.In this study,we revealed a synergistic passivation mechanism on perovskite films by using a dual-functional compound of potassium bromide.The dual functional potassium bromide on the one hand can passivate the defects of halide vacancies with bromine anions and,on the other hand,can screen the charged defects at the grain boundaries with potassium cations.This approach effectively reduces the probability of carriers quenching resulting from charged defects capture and consequently enhances the radiative recombination efficiency of perovskite thin films,leading to a significant enhancement of photoluminescence quantum yield to near-unity values(95%).Meanwhile,the potassium bromide treatment promoted the growth of homogeneous and smooth film,facilitating the charge carrier injection in the devices.Consequently,the perovskite light-emitting diodes based on this strategy achieve a maximum external quantum efficiency of~21%and maximum luminance of~60,000 cd m^(-2).This work provides a deeper insight into the passivation mechanism of ionic compound additives in perovskite with the solution method.
基金supported by the National Natural Science Foundation of China-Yunnan Joint Fund(U1902222)the National Natural Science Foundation of China(11774138,11664022,51862020 and 11804255)+1 种基金the Foundation of Yunnan Province(2019HC016)the project for personal training fund supported by Kunming University of Science and Technology(KKSY201632046).
文摘The non-radiative loss in a perovskite,mainly resulting from thermal defects and halogen vacancies,has always been an important factor affecting its luminescence properties.The addition of a lithium ion has been demonstrated to be an effective way to reduce the nonradiative recombination in perovskitefilms,mainly acting on the surface/interface of thefilms.However,few studies have focused on its role in col loidal quantum dots.Herein,we have used LiBr as a new dual-defect passivation agent in colloidal CsPbX_(3)(X=Br andⅠ)quantum dots to reduce the capture ability of the defects for excited electrons,leading to an effective reduction of the non-radiative recombination.The mechanism of LiBr doping in CsPbX_(3)(X=Br andⅠ)quantum dots was studied by exploring its photodynamic process at room temperature and low temperature.Our results show that an appropriate concentration of LiBr can not only passivate the halide vacancy and thermal defect to reduce the nonradiative recombination,but also improve the phase stabi lity caused by halide migration.
文摘Correction for‘The dual-defect passivation role of lithium bromide doping in reducing the nonradiative loss in CsPbX_(3)(X=Br and I)quantum dots’by Hao Wu et al.,Inorg.Chem.Front.,2020,DOI:10.1039/d0qi01262a.
基金funded by the National Natural Science Foundation of China(Grant No.12204256 and 12147121)supported by the Ningbo Yongjiang Talent Programme of China(2023A-156-G).DFT simulations were carried out at the Supercomputer Center of NBU.
文摘Lead-iodine perovskites are emerging as promising candidates for next-generation solar cells,yet a divergence persists between the theoretical and experimental realms regarding the impact of surface iodine vacancies(V_(I))on device performance.To elevate cell efficiency,a profound understanding and delicate control of V_(I) and their passivation mechanisms are crucial.In this work,we studied various V_(I) defects near the surface of all-inorganic CsPbI3 perovskite using ab initio non-adiabatic molecular dynamics.The results show that the electron-hole(e-h)recombination lifetime highly depends on the defect positions and configurations,as well as the efficacy of Lewis base additives in passivating defects.Despite the outermost layer V_(I) creating no defect state within the band gap,the carrier recombination rate accelerates significantly by a factor of 2 compared to that with the defect-free surface,owing to strong electron-phonon coupling.Subsurface defects create a localized hole trapping state,enabling swift capture of valence band holes,which subsequently accelerate recombination with the conduction band electrons by a factor of 6.5.Remarkably for Pb-dimers,this rate escalates 13-fold.Incorporating the Lewis base molecule HCOO-forms the stable Pb-O bonds with lead ions,preventing surface V_(I) reconstruction(iodine migration),Pb-dimer formation,and an in-band defect state.These effectively reduce the electron-phonon coupling,achieving performance comparable to that of the defect-free surface.This work reconciles contradictory of surface V_(I) on perovskite performance,and enriches our understanding of surface defect properties and their effects on carrier dynamics and device efficiency.
基金financially supported by the National Ten Thousand Talent Program (H.C.)。
文摘Cesium lead iodide perovskites offer promising stability and a bandgap near 1.7 eV,making them suitable as the top cell in tandem solar cells.However,the inorganic perovskite films suffer from a high defect density and substantial recombination losses,undermining their optoelectronic performances.Here,by activating the aromatic system,we develop 4-methoxybenzoylhydrazine(MeOBH)-modified CsPbI_(3) film with regulated crystallinity,suppressed non-radiative recombination,and improved interfacial energetic alignment.The resultant inorganic perovskite solar cells achieved a power conversion efficiency of 20.95%,along with enhanced phase stability owing to the strong coordination interaction between the lead cation and the hydrazide group.Encapsulated devices retain 90.4% of the initial performance after 624 h of maximum power point operation under the ISOS-L-1I protocol.
基金National Natural Science Foundation of China(No.22065038)High-Level Talents Introduction in Yunnan Province(No.C619300A010)+3 种基金the Fund for Excellent Young Scholars of Yunnan(No.202001AW070008)Spring City Plan:the Highlevel Talent Promotion and Training Project of Kunming(No.2022SCP005)for financial supportthe support from the Postdoctoral Research Foundation of Yunnan University(No.W8223004)the Postdoctoral Foundation of Department of Human Resources and Social Security of Yunnan Province(No.C615300504046)。
文摘Defects at the grain boundaries(GBs)of perovskite film highly restrict both the efficiency and stability of perovskite solar cells(PSCs).Herein,organic small molecules of butanedioic acid(BA)and acetylenedicarboxylic acid(AA),containing two carbonyl(C=O)groups and different core-units,were incorporated into perovskite as additives for PSCs application.Thanks to the strong coordination interaction between C=O group and under-coordinated Pb^(2+),the additives can effectively passivate film defects and regulate the perovskite crystallization,yielding high-quality perovskite films with lower defect densities.More importantly,the additives can efficiently regulate the charge transport behaviors in PSCs.Benefiting from the defects passivation and the regulation of charge carrier dynamics,the BA and AA-treaded PSCs show the power conversion efficiencies of 21.52%and 20.50%,which are higher than that of the control device(19.41%).Besides,the optimal devices exhibit a remarkable enhanced long-term stability and moisture tolerance compared to the pristine devices.Furthermore,the transient absorption spectrum reveals the mechanism of enhanced photovoltaic performances,attributing to the improvement of charge transport capability at the perovskite/Spiro-OMeTAD interfaces.This work affords a promising strategy to improve the efficiency and stability of PSCs through regulating the charge-carrier dynamic process in perovskite film.
基金financially supported by the Defense Industrial Technology Development Program(JCKY2017110C0654)the National Natural Science Foundation of China(11974063,61904023)the Chongqing Special Postdoctoral Science Foundation(cstc2019jcyj-bsh0026)。
文摘Bulk and interface carrier nonradiative recombination losses impede the further improvement of power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs).It is highly necessary to develop multifunctional strategy to minimize surface and interface nonradiative recombination losses.Herein,we report a bulk and interface defect passivation strategy via the synergistic effect of anions and cations,where multifunctional potassium sulphate(K_(2)SO_(4))is incorporated at SnO_(2)/perovskite interface.We find that K^(+)ions in K_(2)SO_(4)diffuse into perovskite layer and suppress the formation of bulk defects in perovskite films,and the SO_(4)^(2-)ions remain located at interface via the strong chemical interaction with SnO_(2)layer and perovskite layer,respectively.Through this synergistic modification strategy,effective defect passivation and improved energy band alignment are achieved simultaneously.These beneficial effects are translated into an efficiency increase from 19.45%to 21.18%with a low voltage deficit of0.53 V mainly as a result of boosted open-circuit voltage(V_(oc))after K_(2)SO_(4)modification.In addition,the K_(2)SO_(4)modification contributes to ameliorated stability.The present work provides a route to minimize bulk and interface nonradiative recombination losses for the simultaneous realization of PCE and stability enhancement by rational anion and cation synergistic engineering.
基金the National Key Research and Development Program of China(2016YFA0202400 and 2016YFA0202404)the National Natural Science Foundation of China(61904076 and U19A2089)+3 种基金the Natural Science Foundation of Guangdong Province(2020A1515010980 and 2019B1515120083)the Peacock Team Project funding from the Shenzhen Science and Technology Innovation Committee(KQTD2015033110182370)the Shenzhen Engineering R&D Center for Flexible Solar Cells Project funding from Shenzhen Development and Reform Committee(2019-126)the GuangdongHong Kong-Macao Joint Laboratory(2019B121205001)。
文摘Surface and grain boundary defects in halide perovskite solar cells are highly detrimental,reducing efficiencies and stabilities.Widespread halide anion and organic cation defects usually aggravate ion diffusion and material degradation on the surfaces and at the grain boundaries of perovskite films.In this study,we employ an in-situ green method utilizing nontoxic cetyltrimethylammonium chloride(CTAC)and isopropanol(IPA)as anti-solvents to effectively passivate both surface and grain boundary defects in hybrid perovskites.Anion vacancies can be readily passivated by the chloride group due to its high electronegativity,and cation defects can be synchronously passivated by the more stable cetyltrimethylammonium group.The results show that the charge trap density was significantly reduced,while the carrier recombination lifetime was markedly extended.As a result,the power conversion efficiency of the cell can reach 23.4%with this in-situ green method.In addition,the device retains 85%of its original power conversion efficiency after 600 h of operation under illumination,showing that the stability of perovskite solar cells is improved with this in-situ passivation strategy.This work may provide a green and effective route to improve both the stability and efficiency of perovskite solar cells.
