Organic-inorganic hybrid metal halide perovskite solar cells(PSCs)have attracted much attention due to their high photoelectric conversion efficiency(PCE)and low cost.The certificated PCE of small active area(below 0....Organic-inorganic hybrid metal halide perovskite solar cells(PSCs)have attracted much attention due to their high photoelectric conversion efficiency(PCE)and low cost.The certificated PCE of small active area(below 0.1 cm^(2))device has reached 26.7%[1].However,when considering the scaled-up commercialization of PSCs,an obvious efficiency drop exists for the translation to large-area perovskite submodules(PSMs)with areas more than 200 cm^(2),thus limiting the practical commercialization[2].The major PCE gap between small area cells and large area modules arises the drop of open-circuit voltage(VOC)and fill factor(FF).Formamidinium lead iodide(FAPbI_(3))is now the mostly widely used and highly efficient perovskite composition.However,the photo-active black α-FAPbI_(3) phase will spontaneously transform into photo-inactive yellowδ-FAPbI_(3) phase at room temperature[3].展开更多
Poly(3-hexylthiophene)(P3HT)is one of the most promising hole-transporting materials in the pursuit of efficient and stable perovskite solar cells due to its outstanding stability and low cost.However,the intrinsic lo...Poly(3-hexylthiophene)(P3HT)is one of the most promising hole-transporting materials in the pursuit of efficient and stable perovskite solar cells due to its outstanding stability and low cost.However,the intrinsic low carrier density of P3 HT and poor contact between the P3HT/perovskite interface always lead to a low performance of the solar cell,while conventional chemical doping always makes the films unstable and limits the scalability.In this work,for the first time,we simultaneously enhanced the hole transporting properties of P3HT film and the interface of perovskite by doping it with a judiciously designed oxidized small molecule organic semiconductor.The organic salt not only can promote the lamellar crystallinity of P3HT to obtain better charge transport properties,but also reduce the defects of perovskite.As a result,we achieved champion efficiencies of 23.0%for small-area solar cells and 18.8%for larger-area modules(48.0 cm^(2)).This efficiency is the highest value for P3HT-based perovskite modules.Moreover,the solar cells show excellent operational stability,retaining over 95%of their initial efficiencies after1200 h of continuous operation.展开更多
Back interface passivation reduces the back recombination of photogenerated electrons, whereas aggravates the blocking of hole transport towards back contact, which complicate the back interface engineering for ultrat...Back interface passivation reduces the back recombination of photogenerated electrons, whereas aggravates the blocking of hole transport towards back contact, which complicate the back interface engineering for ultrathin CIGSe solar cells with a Schottky back contact. In this work, theoretical explorations were conducted to study how the two contradictory electrical effects impact cell performance. For ultrathin CIGSe solar cells with a pronounced Schottky potential barrier(E_(h)> 0.2 eV), back interface passivation produces diverse performance evolution trends, which are highly dependent on cell structures and properties. Since a back Ga grading can screen the effect of reduced recombination of photogenerated electrons from back interface passivation, the hole blocking effect predominates and back interface passivation is not desirable. However, when the back Schottky diode merges with the main pn junction due to a reduced absorber thickness,the back potential barrier and the hole blocking effect is much reduced on this occasion. Consequently, cells exhibit the same efficiency evolution trend as ones with an Ohmic contact, where back interface passivation is always advantageous.The discoveries imply the complexity of back interface passivation and provide guidance to manipulate back interface for ultrathin CIGSe solar on TCOs with a pronounced Schottky back contact.展开更多
The allure of high efficiency and low-temperature solution-processed organic-inorganic hybrid perovskite solar cells(PSCs)are inspiring scientists to seek for its commercialization.Interface passivation engineering ha...The allure of high efficiency and low-temperature solution-processed organic-inorganic hybrid perovskite solar cells(PSCs)are inspiring scientists to seek for its commercialization.Interface passivation engineering has become an effective way to further enhance the efficiency and stability of PSCs by defect passivation,reduces the charge recombination and ion migration initiation and hysteresis control,etc.Herein,we have summarized the effects and recent research progress of interface passivation engineering in PSCs.Interface passivation layers can be realized by using the solution and/or vacuum evaporation processes which are very adaptable to varied materials with different properties and fabrication processes for enhanced photovoltaic performance and stability.展开更多
GaAs metal–oxide–semiconductor（MOS） capacitors with HfTiO as the gate dielectric and Al2O3 or ZnO as the interface passivation layer（IPL） are fabricated. X-ray photoelectron spectroscopy reveals that the Al2O3 I...GaAs metal–oxide–semiconductor（MOS） capacitors with HfTiO as the gate dielectric and Al2O3 or ZnO as the interface passivation layer（IPL） are fabricated. X-ray photoelectron spectroscopy reveals that the Al2O3 IPL is more effective in suppressing the formation of native oxides and As diffusion than the ZnO IPL. Consequently, experimental results show that the device with Al2O3 IPL exhibits better interfacial and electrical properties than the device with ZnO IPL： lower interface-state density（7.2×10^12 eV1cm^2/, lower leakage current density（3.60×10^7A/cm^2 at Vg D1 V） and good C–V behavior.展开更多
Tin dioxide(SnO_(2))has been demonstrated as one of the promising electron transport layers for high-efficiency perovskite solar cells(PSCs).However,scalable fabrication of SnO_(2) films with uniform coverage,desirabl...Tin dioxide(SnO_(2))has been demonstrated as one of the promising electron transport layers for high-efficiency perovskite solar cells(PSCs).However,scalable fabrication of SnO_(2) films with uniform coverage,desirable thickness and a low defect density in perovskite solar mod-ules(PSMs)is still challenging.Here,we report preparation of high-quality large-area SnO_(2) films by chemical bath depo-sition(CBD)with the addition of KMnO_(4).The strong oxidiz-ing nature of KMnO_(4) promotes the conversion from Sn(II)to Sn(VI),leading to reduced trap defects and a higher carrier mobility of SnO_(2).In addition,K ions diffuse into the per-ovskite film resulting in larger grain sizes,passivated grain boundaries,and reduced hysteresis of PSCs.Furthermore,Mn ion doping improves both the crystallinity and the phase stability of the perovskite film.Such a multifunctional interface engineering strategy enabled us to achieve a power conversion efficiency(PCE)of 21.70% with less hysteresis for lab-scale PSCs.Using this method,we also fabricated 5×5 and 10×10 cm^(2) PSMs,which showed PCEs of 15.62% and 11.80%(active area PCEs are 17.26%and 13.72%),respectively.For the encapsulated 5×5 cm^(2) PSM,we obtained a T80 operation lifetime(the lifespan during which the solar module PCE drops to 80%of its initial value)exceeding 1000 h in ambient condition.展开更多
For the global commercialization of highly efficient and stable perovskite solar cells(PSCs),it is necessary to effectively suppress the formation of various defects acting as nonradiative recombination sources in per...For the global commercialization of highly efficient and stable perovskite solar cells(PSCs),it is necessary to effectively suppress the formation of various defects acting as nonradiative recombination sources in perovskite light-harvesting materials.Interfacial defects between the charge-selective layer and the perovskite are easily formed in the solution process used to fabricate perovskite films.In addition,owing to the difference in thermal expansion coefficients between the substrate and the perovskite film,internal residual tensile stress inevitably occurs,resulting in increased nonradiative recombination.Herein,a simple compositional engineering scheme for realizing efficient and stable PSCs,which incorporates acetamidinium bromide(AABr)as an additive into the MAPbI_(3) lattice,is proposed.As an additive,AABr has been found to provide synergistic multiple passivation for both internal and interfacial defects.AABr was found to effectively release the tensile strain of the MAPbI_(3) film by forming a structure stabilized by NH-I hydrogen bonds,as evidenced by calculations based on density functional theory(DFT).Furthermore,the incorporated AABr additives created a charge carrier recombination barrier to enhance charge collection capability by reducing interfacial defects.Accordingly,a power conversion efficiency(PCE)of 20.18%was achieved using a planar device employing AABr-incorporated MAPbI_(3).This was substantially higher than the 18.32% PCE of a pristine MAPbI_(3)-based device.Notably,unencapsulated PSCs using AABr-incorporated MAPbI_(3) absorbers exhibited excellent long-term stability,maintaining>95% of initial PCE up to 1200 hours in ambient air.展开更多
NiO has a perfect-aligned energy level with CH3 NH3 Pb I3 perovskite such that it serves as a hole transport layer(HTL),but Ni O-based perovskite solar cells(PSCs)still suffer from low efficiency due to the poor inter...NiO has a perfect-aligned energy level with CH3 NH3 Pb I3 perovskite such that it serves as a hole transport layer(HTL),but Ni O-based perovskite solar cells(PSCs)still suffer from low efficiency due to the poor interface contact between the perovskite layer and the Ni O HTL,and haphazardly stacked perovskite grains.Herein,poly[(9,9-dioctylfluorenyl-2,7-diyl)-alt-co-(1,4-benzo-{2,1,3}-thiadiazole)](PFBT)is introduced between the Ni O and perovskite layers in the form of a polymer aggregate to enhance perovskite crystallinity and decrease the interface charge recombination between perovskite and Ni O in PSCs,resulting in an improved performance.Moreover,PFBT modified perovskite films showed sharper,smoother,and more compact crystalline grains with fewer grain boundaries,leading to the decreased nonradiative recombination.This study offers a simple strategy to achieve highly efficient PSCs with the incorporation of polymer semiconductor aggregates to passivate the interface between the perovskite and Ni O layers.展开更多
Abundant interfacial defects remain a significant challenge that hampers both the efficiency and stability of perovskite solar cells(PSCs).Herein,an alcohol-dispersed conducting polymer complex,denoted as PEDOT:F(Poly...Abundant interfacial defects remain a significant challenge that hampers both the efficiency and stability of perovskite solar cells(PSCs).Herein,an alcohol-dispersed conducting polymer complex,denoted as PEDOT:F(Poly(3,4-ethylene dioxythiophene):Perfluorinated sulfonic acid ionomers),is introduced into the interface between perovskite and hole transporting layer in regular-structured PSCs.PEDOT:F serves as a multi-functional interface layer(filling grain boundaries and covering perovskite's grain-surface)to achieve a robust interaction with organic groups within perovskites,which could induce a structural transformation of PEDOT to increase its conductivity for the efficient hole-transport.Furthermore,the strong interaction between PEDOT and perovskites could promote an effective coupling of undercoordinated Pb~(2+)ions with the lone electron pairs near O&S atoms in PEDOT molecules,thereby enhancing defect passivation.Additionally,PEDOT:F with inherent hydrophobic properties prevents effectively moisture invasion into perovskites for the improved long-term stability of the PSCs.Consequently,the PEDOT:F-based PSCs achieved a champion efficiency of 24.81%,and maintained ca.92%of their initial efficiency after 7680 h of storage in a dry air environment,accompanied by the enhanced photothermal stability.展开更多
Organic light-emitting transistors(OLETs)are gaining increasing attention as a promising candidate for nextgeneration display technology.However,due to the limited horizontal charge transport capability in OLETs,enhan...Organic light-emitting transistors(OLETs)are gaining increasing attention as a promising candidate for nextgeneration display technology.However,due to the limited horizontal charge transport capability in OLETs,enhancing their optical performance remains greatly challenging.In this work,an effective strategy is employed to achieve highperformance OLETs by constructing a two-dimensional molecular-scale passivation layer at the dielectric/channel interface using a promising solution-processed small-molecule material,tetratetracontane(TTC).By controlling the microscopic flows driven by intermolecular interactions near the solution meniscus,molecular self-assembly dynamics are effectively regulated,contributing to a significant transformation in molecular layer stacking mode and enabling the formation of large-area TTC thin films with two-dimensional molecular-scale surface structure and uniform morphology.The introduction of high-quality TTC passivation layer film into the dielectric/channel interface optimizes the film morphologies of overlying channel layer,effectively shields the electrostatic dipole effects at dielectric/channel interface,leading to the synergistic optoelectronic regulation and enhanced optical properties of OLETs.Consequently,high brightness of 10,077.3 cd·m^(-2),high external quantum efficiency(EQE)of 20.46%,and low voltage of 15 V are achieved in the lateral OLET.This work presents a promising approach for two-dimensional molecular-scale small molecule interfaces,and provides an effective strategy for achieving high-performance OLET devices.展开更多
The NiO_(x)/perovskite interface in NiO_(x)-based inverted perovskite solar cells(PSCs)is one of the main issues that restrict device performance and long-term stability,as the unwanted interfacial defects and undesir...The NiO_(x)/perovskite interface in NiO_(x)-based inverted perovskite solar cells(PSCs)is one of the main issues that restrict device performance and long-term stability,as the unwanted interfacial defects and undesirable redox reactions cause severe interfacial non-radiative recombination and open-circuit voltage(Voc)loss.Herein,a series of self-assembled molecules(SAMs)are employed to bind,bridge,and stabilize the NiO_(x)/perovskite interface by regulating the electrostatic potential.Based on systematically theoretical and experimental studies,4-pyrazolecarboxylic acid(4-PCA)is proven as an efficient molecule to simultaneously passivate the NiO_(x)and perovskite surface traps,release the interfacial tensile stress as well as quench the detrimental interface redox reactions,thus effectively suppressing the interfacial non-radiative recombination and enhancing the quality of perovskite crystals.Consequently,the PSCs with 4-PCA treatment exhibited an eminently increased Voc,leading to a significant increase in power conversion efficiency from 21.28%to 23.77%.Furthermore,the unencapsulated devices maintain 92.6%and 81.3%of their initial PCEs after storing in air with a relative humidity of 20%–30%for 1000 h and heating at 65℃for 500 h in a N_(2)-filled glovebox,respectively.展开更多
Perovskite solar cells(PSCs)incorporating 2D/3D heterostructures have exhibited remarkable improvements in both power conversion efficiency and operational stability.Nevertheless,the prevalent spin-coating fabrication...Perovskite solar cells(PSCs)incorporating 2D/3D heterostructures have exhibited remarkable improvements in both power conversion efficiency and operational stability.Nevertheless,the prevalent spin-coating fabrication technique presents formidable challenges for scalable manufacturing processes.Herein,we present a blade-coating compatible methodology for fabricating highperformance 2D/3D PSCs utilizing a low-volatility t-amyl alcohol(t-AmOH)-dimethylformamide(DMF)mixed solvent system.Through systematic materials characterization and comprehensive device performance analysis,we demonstrate that this approach facilitates uniform spatial distribution of butylammonium iodide(BAI)organic spacers,thereby promoting the formation of a high-quality 2D/3D perovskite architecture characterized by enhanced crystallinity and substantially reduced defect density.The optimized device achieves a champion power conversion efficiency of 22.25%while demonstrating exceptional operational stability,retaining 83%of its initial performance after prolonged exposure under ambient conditions(45%relative humidity)for 1000 h.展开更多
Attempts to remove environmentally harmful materials in mass production industries are always a major issue and draw attention if the substitution guarantees a chance to lower fabrication cost and to improve device pe...Attempts to remove environmentally harmful materials in mass production industries are always a major issue and draw attention if the substitution guarantees a chance to lower fabrication cost and to improve device performance,as in a wide bandgap Zn_(1-x)Mg_(x)O(ZMO)to replace the CdS buffer in Cu(In_(1-x),Ga_(x))Se_(2)(CIGSe)thin-film solar cell structure.ZMO is one of the candidates for the buffer material in CIGSe thin-film solar cells with a wide and controllable bandgap depending on the Mg content,which can be helpful in attaining a suitable conduction band offset.Hence,compared to the fixed and limited bandgap of a CdS buffer,a ZMO buffer may provide advantages in V_(oc) and J_(sc) based on its controllable and wide bandgap,even with a relatively wider bandgap CIGSe thin-film solar cell.In addition,to solve problems with the defect sites at the ZMO/CIGSe junction interface,a few-nanometer ZnS layer is employed for heterojunction interface passivation,forming a ZMO/ZnS buffer structure by atomic layer deposition(ALD).Finally,a Cd-free all-dry-processed CIGSe solar cell with a wider bandgap(1.25 eV)and ALD-grown buffer structure exhibited the best power conversion efficiency of 19.1%,which exhibited a higher performance than the CdS counterpart.展开更多
Understanding the role of perovskite surface passivators in hot carriers transfer dynamics is important to develop highly efficient perovskite solar cells(PSCs).In this work,we have designed and synthesized a naphthal...Understanding the role of perovskite surface passivators in hot carriers transfer dynamics is important to develop highly efficient perovskite solar cells(PSCs).In this work,we have designed and synthesized a naphthalimide-based organic small molecule(NCN)for perovskite surface defect passivator.We reveal that the introduction of NCN not only reduces the density of perovskite defect-state,but also promotes hot carriers(HCs)cooling in perovskite through the transient absorption spectroscopy measurements.Fast HCs cooling permits HCs transfer from perovskite layer into NCN layer,thus resulting in the decreased charge-carrier recombination in NCN-treated device.As expected,the power conversion efficiency(PCE)of PSCs with NCN is enhanced to 22.02%from 19.95%for the control device.The findings are relevant for developing highly efficient PSCs.展开更多
The systematic advances in the power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs)have been driven by the developments of perovskite materials,electron transport layer(ETL)materials,and inter...The systematic advances in the power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs)have been driven by the developments of perovskite materials,electron transport layer(ETL)materials,and interfacial passivation between the relevant layers.While zinc oxide(ZnO)is a promising ETL in thin film photovoltaics,it is still highly desirable to develop novel synthetic methods that allow both fine-tuning the versatility of ZnO nanomaterials and improving the ZnO/perovskite interface.Among various inorganic and organic additives,zwitterions have been effectively utilized to passivate the perovskite films.In this vein,we develop novel,well-characterized betaine-coated ZnO QDs and use them as an ETL in the planar n-i-p PSC architecture,combining the ZnO QDs-based ETL with the ZnO/perovskite interface passivation by a series of ammonium halides(NH_(4)X,where X=F,Cl,Br).The champion device with the NH4F passivation achieves one of the highest performances reported for ZnO-based PSCs,exhibiting a maximum PCE of~22%with a high fill factor of 80.3%and competitive stability,retaining~78%of its initial PCE under 1 Sun illumination with maximum power tracking for 250 h.展开更多
ABSTRACT:The severe back interface recombination remains a major performance limiting factor in Cu_(2)ZnSn(S,Se)_(4)(CZTSSe)solar cells.In this work,SiO_(2) nanoparticles deposited on Mo substrate by spin-coating were...ABSTRACT:The severe back interface recombination remains a major performance limiting factor in Cu_(2)ZnSn(S,Se)_(4)(CZTSSe)solar cells.In this work,SiO_(2) nanoparticles deposited on Mo substrate by spin-coating were used to create discrete local contact points to passivate the back interface.Systematic investigation of nanoparticle size reveals that optimized SiO_(2) incorporation enhances absorber crystallinity,reduces interfacial defect density,and suppresses detrimental[2Cu_(Zn)+Sn_(Zn)]deep-level clusters.Meanwhile,it can effectively inhibit nanoparticle agglomeration while maintaining optimal hole-transport distances,thereby obtaining a more efficient porous insulator contact(PIC)passivation structure.We propose that the passivation mechanism involves carrier recombination suppression through minimized defective contact area,thus improving the back contact quality.Consequently,the power conversion efficiency of the ultrathin CZTSSe solar cells increases from 9.03%to 10.72%,offering a viable approach for back-contact engineering.展开更多
Two-terminal(2T)tandem solar cells(TSCs)are optically and electrically connected by two subcells with complementary bandgaps,which are designed to overcome the Shockley-Queisser(S-Q)limit of singlejunction solar cells...Two-terminal(2T)tandem solar cells(TSCs)are optically and electrically connected by two subcells with complementary bandgaps,which are designed to overcome the Shockley-Queisser(S-Q)limit of singlejunction solar cells.Organic-inorganic hybrid perovskites are ideal light-absorbing materials for 2T TSCs due to their tunable bandgaps,low-temperature solution-based processing,and excellent light absorption coefficient.Thus,2T perovskite-based TSCs(PTSCs)have aroused widespread interest among the photovoltaic community.At present,the key to obtaining efficient and stable 2T PTSCs is establishing efficient interfaces and layers with good photoelectric properties and high compatibility of subcells.In particular,interfacial engineering based on effective recombination layers(RCLs)and buffers has a prominent effect on achieving enhanced power conversion efficiency(PCE)of 2T PTSCs with improved operational stability.In this article,the current frontier issues of 2T PTSCs including different device structures and properties are reviewed in detail to analyze their merits,demerits and solutions to overcome bottlenecks.Subsequently,the component engineering,interface engineering and theoretical PCE analysis for designing 2T PTSCs proposed by material simulations are discussed.Furthermore,the scalability of interfacial passivation from single-junction perovskite solar cells to 2T PTSCs is evaluated,and the function mechanisms of RCLs and buffers are also summarized and analyzed carefully.Finally,the challenges faced by 2T PTSCs are pointed out,and their developme nt directions are suggested.This article aims to provide viable guidance for realizing practical manufacturing technologies for the commercialization of 2T PTSCs.展开更多
The interface properties of organic–inorganic mixed halide perovskite solar cells play a significant role in their photovoltaic performance.Defect states at the interface can decrease the power conversion efficiency ...The interface properties of organic–inorganic mixed halide perovskite solar cells play a significant role in their photovoltaic performance.Defect states at the interface can decrease the power conversion efficiency through defect-assisted charge recombination and degrade the long-term stability.Low-dimensional perovskites exhibit excellent stabilities.They can be combined with three dimensional(3D)perovskites to utilize their advantages for fabrication of highperformance devices.In this study,we successfully construct a robust interface for perovskite films through mixed-dimensional engineering.After the introduction of a one dimensional(1D)-structured capping layer on the 3D perovskite through post-treatment,the number of defect states in the perovskite film is significantly decreased,while the lifetime of the photocarriers is increased.In addition,the 1D capping layer can serve as a diffusion barrier to reduce the ion migration and protect the vulnerable 3D perovskite against moisture.Perovskite solar cells based on stacked 1D/3D structures exhibit a power conversion efficiency of 23.3%and maintain 80%of the initial efficiency after storage for over 800 h under ambient conditions with a humidity of 50%.Their performances are superior to those of the 3D devices.This study provides a simple approach to simultaneously enhance the efficiency and stability of perovskite solar cells and may guide the development of other solar cells.展开更多
Despite demonstrating remarkable power conversion efficiencies(PCEs), perovskite solar cells(PSCs) have not yet achieved their full potential. In particular, the interfaces between the perovskite and charge transport ...Despite demonstrating remarkable power conversion efficiencies(PCEs), perovskite solar cells(PSCs) have not yet achieved their full potential. In particular, the interfaces between the perovskite and charge transport layers account for the vast majority of the recombination losses.Interfacial contact and band alignment between the lowtemperature-processed TiO_(2) electron transport layer(ETL)and the perovskite are essential to minimize nonradiative recombination losses. In this study, a CeOx interlayer is employed to modify the perovskite/TiO_(2) interface, and the charge transport properties of the devices are investigated. The bilayer-structured TiO_(2)/CeOx ETL leads to the modification of the interface energetics, resulting in improved electron extraction and reduced nonradiative recombination in the PSCs.Devices based on TiO_(2)/CeOx ETL exhibit a high open-circuit voltage(Voc) of 1.13 V and an enhanced PCE of more than 20%as compared with Vocof 1.08 V and a PCE of approximately 18% for TiO^(2-)based devices. Moreover, PSCs based on TiO_(2)/CeOx ETL maintain over 88% of their initial PCEs after light illumination for 300 min, whereas PSCs based on TiO_(2) ETL almost failed. This study provides an efficient strategy to enhance the PCE and stability of PSCs based on a lowtemperature-processed TiO_(2) ETL.展开更多
基金support from open fund of Fujian Provincial Key Laboratory of Functional Materials and Applications(Xiamen University of Technology,fma2024003)the National Key R&D Program of China(No.2021YFB3500400)the National Natural Science Foundation of China(Nos.52073286 and 22275185).
文摘Organic-inorganic hybrid metal halide perovskite solar cells(PSCs)have attracted much attention due to their high photoelectric conversion efficiency(PCE)and low cost.The certificated PCE of small active area(below 0.1 cm^(2))device has reached 26.7%[1].However,when considering the scaled-up commercialization of PSCs,an obvious efficiency drop exists for the translation to large-area perovskite submodules(PSMs)with areas more than 200 cm^(2),thus limiting the practical commercialization[2].The major PCE gap between small area cells and large area modules arises the drop of open-circuit voltage(VOC)and fill factor(FF).Formamidinium lead iodide(FAPbI_(3))is now the mostly widely used and highly efficient perovskite composition.However,the photo-active black α-FAPbI_(3) phase will spontaneously transform into photo-inactive yellowδ-FAPbI_(3) phase at room temperature[3].
基金financially supported by the National Natural Science Foundation of China(52472248 and 22075221)the Key Research and Development Project of Shanxi Province(202202060301003 and 202202060301015)the Innovation Program of Wuhan-Shuguang Project(2023010201020367)。
文摘Poly(3-hexylthiophene)(P3HT)is one of the most promising hole-transporting materials in the pursuit of efficient and stable perovskite solar cells due to its outstanding stability and low cost.However,the intrinsic low carrier density of P3 HT and poor contact between the P3HT/perovskite interface always lead to a low performance of the solar cell,while conventional chemical doping always makes the films unstable and limits the scalability.In this work,for the first time,we simultaneously enhanced the hole transporting properties of P3HT film and the interface of perovskite by doping it with a judiciously designed oxidized small molecule organic semiconductor.The organic salt not only can promote the lamellar crystallinity of P3HT to obtain better charge transport properties,but also reduce the defects of perovskite.As a result,we achieved champion efficiencies of 23.0%for small-area solar cells and 18.8%for larger-area modules(48.0 cm^(2)).This efficiency is the highest value for P3HT-based perovskite modules.Moreover,the solar cells show excellent operational stability,retaining over 95%of their initial efficiencies after1200 h of continuous operation.
基金Project supported by the National Natural Science Foundation of China (Grant No. 51802240)。
文摘Back interface passivation reduces the back recombination of photogenerated electrons, whereas aggravates the blocking of hole transport towards back contact, which complicate the back interface engineering for ultrathin CIGSe solar cells with a Schottky back contact. In this work, theoretical explorations were conducted to study how the two contradictory electrical effects impact cell performance. For ultrathin CIGSe solar cells with a pronounced Schottky potential barrier(E_(h)> 0.2 eV), back interface passivation produces diverse performance evolution trends, which are highly dependent on cell structures and properties. Since a back Ga grading can screen the effect of reduced recombination of photogenerated electrons from back interface passivation, the hole blocking effect predominates and back interface passivation is not desirable. However, when the back Schottky diode merges with the main pn junction due to a reduced absorber thickness,the back potential barrier and the hole blocking effect is much reduced on this occasion. Consequently, cells exhibit the same efficiency evolution trend as ones with an Ohmic contact, where back interface passivation is always advantageous.The discoveries imply the complexity of back interface passivation and provide guidance to manipulate back interface for ultrathin CIGSe solar on TCOs with a pronounced Schottky back contact.
基金the National Key Research and Development Plan(2017YFE0131900,2019YFE0107200)National Natural Science Foundation of China(52072284)+2 种基金the Fundamental Research Funds for the Central Universities(WUT:202443004)the Technological Innovation Key Project of Hubei Province(2018AAA048).J.Z.thanks the support the“Chutian Scholar Program”of Hubei Province,China.
文摘The allure of high efficiency and low-temperature solution-processed organic-inorganic hybrid perovskite solar cells(PSCs)are inspiring scientists to seek for its commercialization.Interface passivation engineering has become an effective way to further enhance the efficiency and stability of PSCs by defect passivation,reduces the charge recombination and ion migration initiation and hysteresis control,etc.Herein,we have summarized the effects and recent research progress of interface passivation engineering in PSCs.Interface passivation layers can be realized by using the solution and/or vacuum evaporation processes which are very adaptable to varied materials with different properties and fabrication processes for enhanced photovoltaic performance and stability.
基金Project supported by the National Natural Science Foundation of China(Nos.61176100,61274112)
文摘GaAs metal–oxide–semiconductor（MOS） capacitors with HfTiO as the gate dielectric and Al2O3 or ZnO as the interface passivation layer（IPL） are fabricated. X-ray photoelectron spectroscopy reveals that the Al2O3 IPL is more effective in suppressing the formation of native oxides and As diffusion than the ZnO IPL. Consequently, experimental results show that the device with Al2O3 IPL exhibits better interfacial and electrical properties than the device with ZnO IPL： lower interface-state density（7.2×10^12 eV1cm^2/, lower leakage current density（3.60×10^7A/cm^2 at Vg D1 V） and good C–V behavior.
基金supported by funding from the Energy Materials and Surface Sciences Unit of the Okinawa Institute of Science and Technology Graduate Universitythe OIST R&D Cluster Research Program,the OIST Proof of Concept(POC)ProgramJST A-STEP Grant Number JPMJTM20HS,Japan。
文摘Tin dioxide(SnO_(2))has been demonstrated as one of the promising electron transport layers for high-efficiency perovskite solar cells(PSCs).However,scalable fabrication of SnO_(2) films with uniform coverage,desirable thickness and a low defect density in perovskite solar mod-ules(PSMs)is still challenging.Here,we report preparation of high-quality large-area SnO_(2) films by chemical bath depo-sition(CBD)with the addition of KMnO_(4).The strong oxidiz-ing nature of KMnO_(4) promotes the conversion from Sn(II)to Sn(VI),leading to reduced trap defects and a higher carrier mobility of SnO_(2).In addition,K ions diffuse into the per-ovskite film resulting in larger grain sizes,passivated grain boundaries,and reduced hysteresis of PSCs.Furthermore,Mn ion doping improves both the crystallinity and the phase stability of the perovskite film.Such a multifunctional interface engineering strategy enabled us to achieve a power conversion efficiency(PCE)of 21.70% with less hysteresis for lab-scale PSCs.Using this method,we also fabricated 5×5 and 10×10 cm^(2) PSMs,which showed PCEs of 15.62% and 11.80%(active area PCEs are 17.26%and 13.72%),respectively.For the encapsulated 5×5 cm^(2) PSM,we obtained a T80 operation lifetime(the lifespan during which the solar module PCE drops to 80%of its initial value)exceeding 1000 h in ambient condition.
基金supported by the Basic Science Research Program through the National Research Foundation of Korea(NRF)funded by the Ministry of Science and ICT(2020R1F1A1068664)。
文摘For the global commercialization of highly efficient and stable perovskite solar cells(PSCs),it is necessary to effectively suppress the formation of various defects acting as nonradiative recombination sources in perovskite light-harvesting materials.Interfacial defects between the charge-selective layer and the perovskite are easily formed in the solution process used to fabricate perovskite films.In addition,owing to the difference in thermal expansion coefficients between the substrate and the perovskite film,internal residual tensile stress inevitably occurs,resulting in increased nonradiative recombination.Herein,a simple compositional engineering scheme for realizing efficient and stable PSCs,which incorporates acetamidinium bromide(AABr)as an additive into the MAPbI_(3) lattice,is proposed.As an additive,AABr has been found to provide synergistic multiple passivation for both internal and interfacial defects.AABr was found to effectively release the tensile strain of the MAPbI_(3) film by forming a structure stabilized by NH-I hydrogen bonds,as evidenced by calculations based on density functional theory(DFT).Furthermore,the incorporated AABr additives created a charge carrier recombination barrier to enhance charge collection capability by reducing interfacial defects.Accordingly,a power conversion efficiency(PCE)of 20.18%was achieved using a planar device employing AABr-incorporated MAPbI_(3).This was substantially higher than the 18.32% PCE of a pristine MAPbI_(3)-based device.Notably,unencapsulated PSCs using AABr-incorporated MAPbI_(3) absorbers exhibited excellent long-term stability,maintaining>95% of initial PCE up to 1200 hours in ambient air.
基金National Natural Science Foundation of China(61875072)National Postdoctoral Program for Innovative Talents(BX20190135)+2 种基金the Special Project of the Province-University Co-constructing Program of Jilin Province(SXGJXX2017-3)Project of Graduate Innovation Fund of Jilin University(101832018C018)International Cooperation and Exchange Project of Jilin Province(20170414002GH,20180414001GH)for the support to the work。
文摘NiO has a perfect-aligned energy level with CH3 NH3 Pb I3 perovskite such that it serves as a hole transport layer(HTL),but Ni O-based perovskite solar cells(PSCs)still suffer from low efficiency due to the poor interface contact between the perovskite layer and the Ni O HTL,and haphazardly stacked perovskite grains.Herein,poly[(9,9-dioctylfluorenyl-2,7-diyl)-alt-co-(1,4-benzo-{2,1,3}-thiadiazole)](PFBT)is introduced between the Ni O and perovskite layers in the form of a polymer aggregate to enhance perovskite crystallinity and decrease the interface charge recombination between perovskite and Ni O in PSCs,resulting in an improved performance.Moreover,PFBT modified perovskite films showed sharper,smoother,and more compact crystalline grains with fewer grain boundaries,leading to the decreased nonradiative recombination.This study offers a simple strategy to achieve highly efficient PSCs with the incorporation of polymer semiconductor aggregates to passivate the interface between the perovskite and Ni O layers.
基金supported by the Science Foundation(K201827)the Open Foundation of Hubei Key Laboratory of Optical Information and Pattern Recognition(202103,202206)the Graduate Education Innovation Fund of Wuhan Institute of Technology(CX2023279,CX2023277,CX2023272)。
文摘Abundant interfacial defects remain a significant challenge that hampers both the efficiency and stability of perovskite solar cells(PSCs).Herein,an alcohol-dispersed conducting polymer complex,denoted as PEDOT:F(Poly(3,4-ethylene dioxythiophene):Perfluorinated sulfonic acid ionomers),is introduced into the interface between perovskite and hole transporting layer in regular-structured PSCs.PEDOT:F serves as a multi-functional interface layer(filling grain boundaries and covering perovskite's grain-surface)to achieve a robust interaction with organic groups within perovskites,which could induce a structural transformation of PEDOT to increase its conductivity for the efficient hole-transport.Furthermore,the strong interaction between PEDOT and perovskites could promote an effective coupling of undercoordinated Pb~(2+)ions with the lone electron pairs near O&S atoms in PEDOT molecules,thereby enhancing defect passivation.Additionally,PEDOT:F with inherent hydrophobic properties prevents effectively moisture invasion into perovskites for the improved long-term stability of the PSCs.Consequently,the PEDOT:F-based PSCs achieved a champion efficiency of 24.81%,and maintained ca.92%of their initial efficiency after 7680 h of storage in a dry air environment,accompanied by the enhanced photothermal stability.
基金supported by the National Natural Science Foundation of China(Nos.62474011 and 62204006)Shenzhen Science and Technology Program(No.RCBS20231211090701006)+2 种基金Development and Reform Commission of Shenzhen Municipality(No.XMHT20220106002)Guangdong Key Laboratory of Flexible Optoelectronic Materials and Devices,Guangdong International Science Collaboration Base(No.2019A050505003)Shenzhen Key Laboratory of Organic Opto-electromagnetic Functional Materials of Shenzhen Science and Technology Plan(No.ZDSYS20140509094114164).
文摘Organic light-emitting transistors(OLETs)are gaining increasing attention as a promising candidate for nextgeneration display technology.However,due to the limited horizontal charge transport capability in OLETs,enhancing their optical performance remains greatly challenging.In this work,an effective strategy is employed to achieve highperformance OLETs by constructing a two-dimensional molecular-scale passivation layer at the dielectric/channel interface using a promising solution-processed small-molecule material,tetratetracontane(TTC).By controlling the microscopic flows driven by intermolecular interactions near the solution meniscus,molecular self-assembly dynamics are effectively regulated,contributing to a significant transformation in molecular layer stacking mode and enabling the formation of large-area TTC thin films with two-dimensional molecular-scale surface structure and uniform morphology.The introduction of high-quality TTC passivation layer film into the dielectric/channel interface optimizes the film morphologies of overlying channel layer,effectively shields the electrostatic dipole effects at dielectric/channel interface,leading to the synergistic optoelectronic regulation and enhanced optical properties of OLETs.Consequently,high brightness of 10,077.3 cd·m^(-2),high external quantum efficiency(EQE)of 20.46%,and low voltage of 15 V are achieved in the lateral OLET.This work presents a promising approach for two-dimensional molecular-scale small molecule interfaces,and provides an effective strategy for achieving high-performance OLET devices.
基金financially supported by the National Natural Science Foundation of China (U22A2078)Fundamental Research Funds for the Central Universities (2022CDJQY-007)
文摘The NiO_(x)/perovskite interface in NiO_(x)-based inverted perovskite solar cells(PSCs)is one of the main issues that restrict device performance and long-term stability,as the unwanted interfacial defects and undesirable redox reactions cause severe interfacial non-radiative recombination and open-circuit voltage(Voc)loss.Herein,a series of self-assembled molecules(SAMs)are employed to bind,bridge,and stabilize the NiO_(x)/perovskite interface by regulating the electrostatic potential.Based on systematically theoretical and experimental studies,4-pyrazolecarboxylic acid(4-PCA)is proven as an efficient molecule to simultaneously passivate the NiO_(x)and perovskite surface traps,release the interfacial tensile stress as well as quench the detrimental interface redox reactions,thus effectively suppressing the interfacial non-radiative recombination and enhancing the quality of perovskite crystals.Consequently,the PSCs with 4-PCA treatment exhibited an eminently increased Voc,leading to a significant increase in power conversion efficiency from 21.28%to 23.77%.Furthermore,the unencapsulated devices maintain 92.6%and 81.3%of their initial PCEs after storing in air with a relative humidity of 20%–30%for 1000 h and heating at 65℃for 500 h in a N_(2)-filled glovebox,respectively.
基金supported by ational Natural Science Foundation of China(Nos.62405293,62301509,62304209)Key Research and Development Program of Shanxi Province(No.202302030201001)Fundamental Research Program of Shanxi Province(Nos.202303021212191,202203021222079,20210302123203,202103021223185).
文摘Perovskite solar cells(PSCs)incorporating 2D/3D heterostructures have exhibited remarkable improvements in both power conversion efficiency and operational stability.Nevertheless,the prevalent spin-coating fabrication technique presents formidable challenges for scalable manufacturing processes.Herein,we present a blade-coating compatible methodology for fabricating highperformance 2D/3D PSCs utilizing a low-volatility t-amyl alcohol(t-AmOH)-dimethylformamide(DMF)mixed solvent system.Through systematic materials characterization and comprehensive device performance analysis,we demonstrate that this approach facilitates uniform spatial distribution of butylammonium iodide(BAI)organic spacers,thereby promoting the formation of a high-quality 2D/3D perovskite architecture characterized by enhanced crystallinity and substantially reduced defect density.The optimized device achieves a champion power conversion efficiency of 22.25%while demonstrating exceptional operational stability,retaining 83%of its initial performance after prolonged exposure under ambient conditions(45%relative humidity)for 1000 h.
基金conducted under the framework of the research and development program of the Korea Institute of Energy Research(C4-2412 and C4-2413)supported by the National Research Foundation of Korea(grant number 2022M3J1A1063019)funded by the Ministry of Science and ICT.
文摘Attempts to remove environmentally harmful materials in mass production industries are always a major issue and draw attention if the substitution guarantees a chance to lower fabrication cost and to improve device performance,as in a wide bandgap Zn_(1-x)Mg_(x)O(ZMO)to replace the CdS buffer in Cu(In_(1-x),Ga_(x))Se_(2)(CIGSe)thin-film solar cell structure.ZMO is one of the candidates for the buffer material in CIGSe thin-film solar cells with a wide and controllable bandgap depending on the Mg content,which can be helpful in attaining a suitable conduction band offset.Hence,compared to the fixed and limited bandgap of a CdS buffer,a ZMO buffer may provide advantages in V_(oc) and J_(sc) based on its controllable and wide bandgap,even with a relatively wider bandgap CIGSe thin-film solar cell.In addition,to solve problems with the defect sites at the ZMO/CIGSe junction interface,a few-nanometer ZnS layer is employed for heterojunction interface passivation,forming a ZMO/ZnS buffer structure by atomic layer deposition(ALD).Finally,a Cd-free all-dry-processed CIGSe solar cell with a wider bandgap(1.25 eV)and ALD-grown buffer structure exhibited the best power conversion efficiency of 19.1%,which exhibited a higher performance than the CdS counterpart.
基金High-Level Talents Introduction in Yunnan Province(No.C619300A010)the Fund for Excellent Young Scholars of Yunnan(No.202001AW070008)+5 种基金Spring City Plan:the High-level Talent Promotion and Training Project of Kunming(No.2022SCP005)for financial supportsupport from the Postdoctoral Foundation of Department of Human Resources and Social Security of Yunnan Province(No.C615300504046)Postdoctoral Research Foundation of Yunnan University(No.W8223004)the National Natural Science Foundation of China(No.22209144)the Project of Natural Science Foundation of Yunnan(Nos.202101AU070034 and 202101AT070337)the Innovation and Entrepreneurship Training Program for college students(No.202110673032)。
文摘Understanding the role of perovskite surface passivators in hot carriers transfer dynamics is important to develop highly efficient perovskite solar cells(PSCs).In this work,we have designed and synthesized a naphthalimide-based organic small molecule(NCN)for perovskite surface defect passivator.We reveal that the introduction of NCN not only reduces the density of perovskite defect-state,but also promotes hot carriers(HCs)cooling in perovskite through the transient absorption spectroscopy measurements.Fast HCs cooling permits HCs transfer from perovskite layer into NCN layer,thus resulting in the decreased charge-carrier recombination in NCN-treated device.As expected,the power conversion efficiency(PCE)of PSCs with NCN is enhanced to 22.02%from 19.95%for the control device.The findings are relevant for developing highly efficient PSCs.
基金the support from the European Union’s Horizon 2020 research and innovation program under the Marie Sk■odowska-Curie[Grant agreement No.711859]the Polish Ministry of Science and Higher Education from the co-funded project[Grant agreement no.3549/H2020/COFUND2016/2]+4 种基金the support of King Abdulaziz City for Science and Technology(KACST),Saudi Arabiathe financial support by the National Science Centre[Grant MAESTRO 11 No.2019/34/A/ST5/00416]the European Union’s Horizon 2020 Research and Innovation program under the Marie Sk■odowska-Curie[Grant agreement No.843453]the European Union’s Horizon 2020 research and innovation program under Grant Agreement 884444financial support by the Marie Sk■odowska-Curie Action(H2020MSCA-IF-2020,[Project No.101024237])
文摘The systematic advances in the power conversion efficiency(PCE)and stability of perovskite solar cells(PSCs)have been driven by the developments of perovskite materials,electron transport layer(ETL)materials,and interfacial passivation between the relevant layers.While zinc oxide(ZnO)is a promising ETL in thin film photovoltaics,it is still highly desirable to develop novel synthetic methods that allow both fine-tuning the versatility of ZnO nanomaterials and improving the ZnO/perovskite interface.Among various inorganic and organic additives,zwitterions have been effectively utilized to passivate the perovskite films.In this vein,we develop novel,well-characterized betaine-coated ZnO QDs and use them as an ETL in the planar n-i-p PSC architecture,combining the ZnO QDs-based ETL with the ZnO/perovskite interface passivation by a series of ammonium halides(NH_(4)X,where X=F,Cl,Br).The champion device with the NH4F passivation achieves one of the highest performances reported for ZnO-based PSCs,exhibiting a maximum PCE of~22%with a high fill factor of 80.3%and competitive stability,retaining~78%of its initial PCE under 1 Sun illumination with maximum power tracking for 250 h.
基金financial support from the National Natural Science Foundation of China(No.62074168)the Guangdong Basic and Applied Basic Research Foundation(No.2024A1515140104)the funding from the State Key Laboratory of Optoelectronic Materials and Technologies at Sun Yat-Sen University(No.OEMT-2022-ZTS-08).
文摘ABSTRACT:The severe back interface recombination remains a major performance limiting factor in Cu_(2)ZnSn(S,Se)_(4)(CZTSSe)solar cells.In this work,SiO_(2) nanoparticles deposited on Mo substrate by spin-coating were used to create discrete local contact points to passivate the back interface.Systematic investigation of nanoparticle size reveals that optimized SiO_(2) incorporation enhances absorber crystallinity,reduces interfacial defect density,and suppresses detrimental[2Cu_(Zn)+Sn_(Zn)]deep-level clusters.Meanwhile,it can effectively inhibit nanoparticle agglomeration while maintaining optimal hole-transport distances,thereby obtaining a more efficient porous insulator contact(PIC)passivation structure.We propose that the passivation mechanism involves carrier recombination suppression through minimized defective contact area,thus improving the back contact quality.Consequently,the power conversion efficiency of the ultrathin CZTSSe solar cells increases from 9.03%to 10.72%,offering a viable approach for back-contact engineering.
基金financially supported by Guangxi Natural Science Foundation(No.2022GXNSFBA035601)Guangxi Research Foundation for Science and Technology Base and Talent Special(No.AD21220055)+1 种基金the Open Fund from the Key Lab of New Processing Technology for Nonferrous Metals and Materials Ministry of Education/Guangxi Key Laboratory of Optical and Electronic Materials and Devices(No.RZ230000636)the National Natural Science Foundation of China(No.U20A20245)。
文摘Two-terminal(2T)tandem solar cells(TSCs)are optically and electrically connected by two subcells with complementary bandgaps,which are designed to overcome the Shockley-Queisser(S-Q)limit of singlejunction solar cells.Organic-inorganic hybrid perovskites are ideal light-absorbing materials for 2T TSCs due to their tunable bandgaps,low-temperature solution-based processing,and excellent light absorption coefficient.Thus,2T perovskite-based TSCs(PTSCs)have aroused widespread interest among the photovoltaic community.At present,the key to obtaining efficient and stable 2T PTSCs is establishing efficient interfaces and layers with good photoelectric properties and high compatibility of subcells.In particular,interfacial engineering based on effective recombination layers(RCLs)and buffers has a prominent effect on achieving enhanced power conversion efficiency(PCE)of 2T PTSCs with improved operational stability.In this article,the current frontier issues of 2T PTSCs including different device structures and properties are reviewed in detail to analyze their merits,demerits and solutions to overcome bottlenecks.Subsequently,the component engineering,interface engineering and theoretical PCE analysis for designing 2T PTSCs proposed by material simulations are discussed.Furthermore,the scalability of interfacial passivation from single-junction perovskite solar cells to 2T PTSCs is evaluated,and the function mechanisms of RCLs and buffers are also summarized and analyzed carefully.Finally,the challenges faced by 2T PTSCs are pointed out,and their developme nt directions are suggested.This article aims to provide viable guidance for realizing practical manufacturing technologies for the commercialization of 2T PTSCs.
基金National Natural Science Foundation of China,Grant/Award Numbers:51972218,52025028,52172220Priority Academic Program Development(PAPD)of Jiangsu Higher Education Institutions+2 种基金Six Talents Peak Project of Jiangsu Province333 High-level Talents Cultivation Project of Jiangsu Province1000 Youth Talents Plan。
文摘The interface properties of organic–inorganic mixed halide perovskite solar cells play a significant role in their photovoltaic performance.Defect states at the interface can decrease the power conversion efficiency through defect-assisted charge recombination and degrade the long-term stability.Low-dimensional perovskites exhibit excellent stabilities.They can be combined with three dimensional(3D)perovskites to utilize their advantages for fabrication of highperformance devices.In this study,we successfully construct a robust interface for perovskite films through mixed-dimensional engineering.After the introduction of a one dimensional(1D)-structured capping layer on the 3D perovskite through post-treatment,the number of defect states in the perovskite film is significantly decreased,while the lifetime of the photocarriers is increased.In addition,the 1D capping layer can serve as a diffusion barrier to reduce the ion migration and protect the vulnerable 3D perovskite against moisture.Perovskite solar cells based on stacked 1D/3D structures exhibit a power conversion efficiency of 23.3%and maintain 80%of the initial efficiency after storage for over 800 h under ambient conditions with a humidity of 50%.Their performances are superior to those of the 3D devices.This study provides a simple approach to simultaneously enhance the efficiency and stability of perovskite solar cells and may guide the development of other solar cells.
基金supported by the National Key Research and Development Program of China (2018YFB1500101)the 111 Project (B16016)+1 种基金the National Natural Science Foundation of China (U1705256,51702096 and 61904053)the Fundamental Research Funds for the Central Universities (2019MS026,2019MS027 and 2020MS080)。
文摘Despite demonstrating remarkable power conversion efficiencies(PCEs), perovskite solar cells(PSCs) have not yet achieved their full potential. In particular, the interfaces between the perovskite and charge transport layers account for the vast majority of the recombination losses.Interfacial contact and band alignment between the lowtemperature-processed TiO_(2) electron transport layer(ETL)and the perovskite are essential to minimize nonradiative recombination losses. In this study, a CeOx interlayer is employed to modify the perovskite/TiO_(2) interface, and the charge transport properties of the devices are investigated. The bilayer-structured TiO_(2)/CeOx ETL leads to the modification of the interface energetics, resulting in improved electron extraction and reduced nonradiative recombination in the PSCs.Devices based on TiO_(2)/CeOx ETL exhibit a high open-circuit voltage(Voc) of 1.13 V and an enhanced PCE of more than 20%as compared with Vocof 1.08 V and a PCE of approximately 18% for TiO^(2-)based devices. Moreover, PSCs based on TiO_(2)/CeOx ETL maintain over 88% of their initial PCEs after light illumination for 300 min, whereas PSCs based on TiO_(2) ETL almost failed. This study provides an efficient strategy to enhance the PCE and stability of PSCs based on a lowtemperature-processed TiO_(2) ETL.
