The introduction of two-dimensional(2D)perovskite layers on top of three-dimensional(3D)perovskite films enhances the performance and stability of perovskite solar cells(PSCs).However,the electronic effect of the spac...The introduction of two-dimensional(2D)perovskite layers on top of three-dimensional(3D)perovskite films enhances the performance and stability of perovskite solar cells(PSCs).However,the electronic effect of the spacer cation and the quality of the 2D capping layer are critical factors in achieving the required results.In this study,we compared two fluorinated salts:4-(trifluoromethyl)benzamidine hydrochloride(4TF-BA·HCl)and 4-fluorobenzamidine hydrochloride(4F-BA·HCl)to engineer the 3D/2D perovskite films.Surprisingly,4F-BA formed a high-performance 3D/2D heterojunction,while4TF-BA produced an amorphous layer on the perovskite films.Our findings indicate that the balanced intramolecular charge polarization,which leads to effective hydrogen bonding,is more favorable in 4F-BA than in 4TF-BA,promoting the formation of a crystalline 2D perovskite.Nevertheless,4TF-BA managed to improve efficiency to 24%,surpassing the control device,primarily due to the natural passivation capabilities of benzamidine.Interestingly,the devices based on 4F-BA demonstrated an efficiency exceeding 25%with greater longevity under various storage conditions compared to 4TF-BA-based and the control devices.展开更多
In recent years, the research advancements have high-lighted the critical role of the A-site cation in determining the optoelectronic and physicochemical properties of organicinorganic lead halide perovskites. Mixed-c...In recent years, the research advancements have high-lighted the critical role of the A-site cation in determining the optoelectronic and physicochemical properties of organicinorganic lead halide perovskites. Mixed-cation perovskites(MCPs) have been extensively used as absorber thin films in perovskite solar cells(PSCs), achieving high power conversion efficiencies(PCE) over 26%^([1, 2]).展开更多
Halide perovskites have emerged as promising materials for X-ray detection with exceptional properties and reasonable costs.Among them,heterostructures between 3D perovskites and low-dimensional perovskites attract in...Halide perovskites have emerged as promising materials for X-ray detection with exceptional properties and reasonable costs.Among them,heterostructures between 3D perovskites and low-dimensional perovskites attract intensive studies of their advantages due to low-level ion migration and decent stability.However,there is still a lack of methods to precisely construct heterostructures and a fundamental understanding of their structure-dependent optoelectronic properties.Herein,a gas-phase method was developed to grow 2D perovskites directly on 3D perovskites with nanoscale accuracy.In addition,the larger steric hindrance of organic layers of 2D perovskites was proved to enable slower ion migration,which resulted in reduced trap states and better stability.Based on MAPbBr_(3)single crystals with the(PA)_(2)PbBr_(4)capping layer,the X-ray detector achieved a sensitivity of 22,245μC Gy_(air)^(−1)cm^(−2),a response speed of 240μs,and a dark current drift of 1.17.10^(–4)nA cm^(−1)s^(−1)V^(−1),which were among the highest reported for state-of-the-art perovskite-based X-ray detectors.This study presents a precise synthesis method to construct perovskite-based heterostructures.It also brings an in-depth understanding of the relationship between lattice structures and properties,which are beneficial for advancing high-performance and cost-effective X-ray detectors.展开更多
Ambient-air,moisture-assisted annealing is widely used in fabricating perovskite solar cells(PSCs).However,the inherent sensitivity of perovskite intermediate-phase to moisture—due to fast and spontaneous intermolecu...Ambient-air,moisture-assisted annealing is widely used in fabricating perovskite solar cells(PSCs).However,the inherent sensitivity of perovskite intermediate-phase to moisture—due to fast and spontaneous intermolecular exchange reaction—requires strict control of ambient humidity and immediate thermal annealing treatment,raising manufacturing costs and causing fast nucleation of perovskite films.We report herein a self-buffered molecular migration strategy to slow down the intermolecular exchange reaction by introducing a n-butylammonium bromide shielding layer,which limits moisture diffusion into intermediate-phase film.This further endows the notably wide nucleation time and humidity windows for perovskite crystallization in ambient air.Consequently,the optimized 1.68 e V-bandgap n-i-p structured PSC reaches a record-high reverse-scan(RS)PCE of 22.09%.Furthermore,the versatility and applicability of as-proposed self-buffered molecular migration strategy are certified by employing various shielding materials and 1.53 eV-/1.77 eV-bandgap perovskite materials.The n-i-p structured PSCs based on 1.53 eV-and 1.77 eV-bandgap perovskite films achieve outstanding RS PCEs of 25.23%and 19.09%,respectively,both of which are beyond of the state-of-the-art ambient-air processed PSCs.展开更多
Metal halide perovskites(MHPs)with striking electrical and optical properties have appeared at the forefront of semiconductor materials for photocatalytic redox reactions but still suffer from some intrinsic drawbacks...Metal halide perovskites(MHPs)with striking electrical and optical properties have appeared at the forefront of semiconductor materials for photocatalytic redox reactions but still suffer from some intrinsic drawbacks such as inferior stability,severe charge-carrier recombination,and limited active sites.Heterojunctions have recently been widely constructed to improve light absorption,passivate surface for enhanced stability,and promote charge-carrier dynamics of MHPs.However,little attention has been paid to the review of MHPs-based heterojunctions for photocatalytic redox reactions.Here,recent advances of MHPs-based heterojunctions for photocatalytic redox reactions are highlighted.The structure,synthesis,and photophysical properties of MHPs-based heterojunctions are first introduced,including basic principles,categories(such as Schottky junction,type-I,type-II,Z-scheme,and S-scheme junction),and synthesis strategies.MHPs-based heterojunctions for photocatalytic redox reactions are then reviewed in four categories:H2evolution,CO_(2)reduction,pollutant degradation,and organic synthesis.The challenges and prospects in solar-light-driven redox reactions with MHPs-based heterojunctions in the future are finally discussed.展开更多
Perovskite solar cells(PSCs)have emerged as promising photovoltaic technologies owing to their remarkable power conversion efficiency(PCE).However,heat accumulation under continuous illumination remains a critical bot...Perovskite solar cells(PSCs)have emerged as promising photovoltaic technologies owing to their remarkable power conversion efficiency(PCE).However,heat accumulation under continuous illumination remains a critical bottleneck,severely affecting device stability and long-term operational performance.Herein,we present a multifunctional strategy by incorporating highly thermally conductive Ti_(3)C_(2)T_(X) MXene nanosheets into the perovskite layer to simultaneously enhance thermal management and optoelectronic properties.The Ti_(3)C_(2)T_(X) nanosheets,embedded at perovskite grain boundaries,construct efficient thermal conduction pathways,significantly improving the thermal conductivity and diffusivity of the film.This leads to a notable reduction in the device’s steady-state operating temperature from 42.96 to 39.97 under 100 mW cm^(−2) illumination,thereby alleviating heat-induced performance degradation.Beyond thermal regulation,Ti_(3)C_(2)T_(X),with high conductivity and negatively charged surface terminations,also serves as an effective defect passivation agent,reducing trap-assisted recombination,while simultaneously facilitating charge extraction and transport by optimizing interfacial energy alignment.As a result,the Ti_(3)C_(2)T_(X)-modified PSC achieve a champion PCE of 25.13%and exhibit outstanding thermal stability,retaining 80%of the initial PCE after 500 h of thermal aging at 85 and 30±5%relative humidity.(In contrast,control PSC retain only 58%after 200 h.)Moreover,under continuous maximum power point tracking in N2 atmosphere,Ti_(3)C_(2)T_(X)-modified PSC retained 70%of the initial PCE after 500 h,whereas the control PSC drop sharply to 20%.These findings highlight the synergistic role of Ti_(3)C_(2)T_(X) in thermal management and optoelectronic performance,paving the way for the development of high-efficiency and heat-resistant perovskite photovoltaics.展开更多
Crystalline silicon(c-Si)solar cells,though dominating the photovoltaic market,are nearing their theoretical power conversion efficiencies(PCE)limit of 29.4%,necessitating the adoption of multi-junction technology to ...Crystalline silicon(c-Si)solar cells,though dominating the photovoltaic market,are nearing their theoretical power conversion efficiencies(PCE)limit of 29.4%,necessitating the adoption of multi-junction technology to achieve higher performance.Among these,perovskiteon-silicon-based multi-junction solar cells have emerged as a promising alternative,where the perovskite offering tunable bandgaps,superior optoelectronic properties,and cost-effective manufacturing.Recent announced double-junction solar cells(PSDJSCs)have achieved the PCE of 34.85%,surpassing all other double-junction technologies.Encouragingly,the rapid advancements in PSDJSCs have spurred increased research interest in perovskite/perovskite/silicon triple-junction solar cells(PSTJSCs)in 2024.This triple-junction solar cell configuration demonstrates immense potential due to their optimum balance between achieving a high PCE limit and managing device complexity.This review provides a comprehensive analysis of PSTJSCs,covering fundamental principles,and technological milestones.Current challenges,including current mismatch,open-circuit voltage deficits,phase segregation,and stability issues,and their corresponding strategies are also discussed,alongside future directions to achieve long-term stability and high PCE.This work aims to advance the understanding of the development in PSTJSCs,paving the way for their practical implementation.展开更多
Formamidinium lead iodide(FAPbI_(3))perovskite exhibits an impressive X-ray absorption coefficient and a large carrier mobility-lifetime product(μτ),making it as a highly promising candidate for X-ray detection appl...Formamidinium lead iodide(FAPbI_(3))perovskite exhibits an impressive X-ray absorption coefficient and a large carrier mobility-lifetime product(μτ),making it as a highly promising candidate for X-ray detection application.However,the presence of larger FA^(+)cation induces to an expansion of the Pb-I octahedral framework,which unfortunately affects both the stability and charge carrier mobility of the corresponding devices.To address this challenge,we develop a novel low-dimensional(HtrzT)PbI_(3) perovskite featuring a conjugated organic cation(1H-1,2,4-Triazole-3-thiol,HtrzT^(+))which matches well with theα-FAPbI_(3) lattices in two-dimensional plane.Benefiting from the matched lattice between(HtrzT)PbI_(3) andα-FAPbI_(3),the anchored lattice enhances the Pb-I bond strength and effectively mitigates the inherent tensile strain of theα-FAPbI_(3) crystal lattice.The X-ray detector based on(HtrzT)PbI_(3)(1.0)/FAPbI_(3) device achieves a remarkable sensitivity up to 1.83×10^(5)μC Gy_(air)^(−1) cm^(−2),along with a low detection limit of 27.6 nGy_(air) s^(−1),attributed to the release of residual stress,and the enhancement in carrier mobility-lifetime product.Furthermore,the detector exhibits outstanding stability under X-ray irradiation with tolerating doses equivalent to nearly 1.17×10^(6) chest imaging doses.展开更多
Perovskite solar cells have achieved remarkable progress in photovoltaic efficiency.However,interfacial defects at the buried and upper interfaces of perovskite layer remain a critical challenge,leading to charge reco...Perovskite solar cells have achieved remarkable progress in photovoltaic efficiency.However,interfacial defects at the buried and upper interfaces of perovskite layer remain a critical challenge,leading to charge recombination,ion migration,and iodine oxidation.To address this,we propose a novel all-in-one modification strategy employing ammonia borane(BNH6)as a multifunctional complex.By incorporating BNH6 at both buried and upper interfaces simultaneously,we achieve dualinterfacial defect passivation and iodide oxidation suppression through three key mechanisms:(1)hydrolysis-induced interaction with SnO_(2),(2)coordination with Pb^(2+),and(3)inhibition of I−oxidation.This approach significantly enhances device performance,yielding a champion power conversion efficiency(PCE)of 26.43%(certified 25.98%).Furthermore,the unencapsulated device demonstrates prominent enhanced operation stability,maintaining 90%of its initial PCE after 500 h under continuous illumination.Notably,our strategy eliminates the need for separate interface treatments,streamlining fabrication and offering a scalable route toward high-performance perovskite photovoltaics.展开更多
Soft X-ray detectors play a vital role in materials science,high-energy physics and medical imaging.Cs_(2)AgBiBr_(6),a lead-free double perovskite,has gained attention for its excellent optoelectronic properties,stabi...Soft X-ray detectors play a vital role in materials science,high-energy physics and medical imaging.Cs_(2)AgBiBr_(6),a lead-free double perovskite,has gained attention for its excellent optoelectronic properties,stability,and nontoxicity.However,its fast crystallization and requirement for high-temperature annealing(>250℃)often lead to inferior film quality,limiting its application in flexible devices.This study introduces an alloying strategy that significantly improves the quality of Cs_(2)AgBiBr_(6)thin films annealed at a reduced temperature of 150℃.Devices based on the alloyed thin films exhibit an ultra-low dark current of 0.32 nA·cm^(-2)and a quantum efficiency of 725%.Furthermore,the first successful integration of Cs_(2)AgBiBr_(6)with a thinfilm transistor backplane demonstrates its superior imaging performance,indicating that Cs_(2)AgBiBr_(6)is a promising material for next-generation soft X-ray sensors.展开更多
Low-dimensional(LD)halide perovskites have attracted considerable attention due to their distinctive structures and exceptional optoelectronic properties,including high absorption coefficients,extended charge carrier ...Low-dimensional(LD)halide perovskites have attracted considerable attention due to their distinctive structures and exceptional optoelectronic properties,including high absorption coefficients,extended charge carrier diffusion lengths,suppressed non-radiative recombination rates,and intense photoluminescence.A key advantage of LD perovskites is the tunability of their optical and electronic properties through the precise optimization of their structural arrangements and dimensionality.This review systematically examines recent progress in the synthesis and optoelectronic characterizations of LD perovskites,focusing on their structural,optical,and photophysical properties that underpin their versatility in diverse applications.The review further summarizes advancements in LD perovskite-based devices,including resistive memory,artificial synapses,photodetectors,light-emitting diodes,and solar cells.Finally,the challenges associated with stability,scalability,and integration,as well as future prospects,are discussed,emphasizing the potential of LD perovskites to drive breakthroughs in device efficiency and industrial applicability.展开更多
The solution processibility of perovskites provides a costeffective and high-throughput route for fabricating state-of-the-art solar cells.However,the fast kinetics of precursor-to-perovskite transformation is suscept...The solution processibility of perovskites provides a costeffective and high-throughput route for fabricating state-of-the-art solar cells.However,the fast kinetics of precursor-to-perovskite transformation is susceptible to processing conditions,resulting in an uncontrollable variance in device performance.Here,we demonstrate a supramolecule confined approach to reproducibly fabricate perovskite films with an ultrasmooth,electronically homogeneous surface.The assembly of a calixarene capping layer on precursor surface can induce host-vip interactions with solvent molecules to tailor the desolvation kinetics,and initiate the perovskite crystallization from the sharp molecule-precursor interface.These combined effects significantly reduced the spatial variance and extended the processing window of perovskite films.As a result,the standard efficiency deviations of device-to-device and batch-to-batch devices were reduced from 0.64-0.26%to 0.67-0.23%,respectively.In addition,the perovskite films with ultrasmooth top surfaces exhibited photoluminescence quantum yield>10%and surface recombination velocities<100 cm s^(-1)for both interfaces that yielded p-i-n structured solar cells with power conversion efficiency over 25%.展开更多
Halide perovskite materials have received considerable attention for solar cells,LEDs,lasers etc.owing to their controllable physicochemical properties and structural advantages.However,little research has focused on ...Halide perovskite materials have received considerable attention for solar cells,LEDs,lasers etc.owing to their controllable physicochemical properties and structural advantages.However,little research has focused on energy storage and conversion applications,such as use as anodes in lithium-ion batteries.In this paper,all-inorganic lead-free halide perovskite Cs_(3)Bi_(2)Cl_(9)powders were synthesized by the grinding method,and the lattice was successfully adjusted via introducing Mn^(2+).The characterization results show that Mn-ion substitution can cause local lattice distortion to restructure the lattice,which will cause a mixed arrangement of[BiCl_(6)]octahedra to improve the performance of the anode material.This new material can provide a feasible solution for solving the problem of low specific capacity anode materials caused by unstable crystal structures,and also indicates that such perovskites with unique crystal structures and lattice tunability have broad application prospects in lithium-ion batteries.展开更多
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
The rapid advancement of metal halide perovskites can be attributed to their exceptional optoelectronic properties and facile solution processing technique.Noteworthy strides have been achieved in the realm of perovsk...The rapid advancement of metal halide perovskites can be attributed to their exceptional optoelectronic properties and facile solution processing technique.Noteworthy strides have been achieved in the realm of perovskite solar cells(PSCs),with a certified power conversion efficiency(PCE)escalating to 26.7%over the course of a decade,positioning them as promising contenders for next-generation photovoltaic technologies[1].However,the formation of crystal defects,including anion/cation vacancies,Pb–I antisite defects,and uncoordinated Pb^(2+),along the surface and grain boundaries(GBs)of perovskite layers during the solution processing stage poses a significant challenge,compromising the photoelectric performance and stability of PSCs.展开更多
Scalable fabrication of efficient wide-bandgap(WBG)perovskite solar cells(PSCs)is crucial to realize the full commercial potential of tandem solar cells.However,there are challenges in fabricating efficient methylammo...Scalable fabrication of efficient wide-bandgap(WBG)perovskite solar cells(PSCs)is crucial to realize the full commercial potential of tandem solar cells.However,there are challenges in fabricating efficient methylammonium-free(MA-free)WBG PSCs by blade coating,especially its phase separation and films stability.In this work,an MA-free WBG perovskite ink is developed for preparing FA_(0.8)Cs_(0.2)Pb(I_(0.75)Br_(0.25))_(3)films by blade coating in ambient air.Among various A-site iodides,RbI is found to be the most effective in suppressing the precipitation of PbI_(2)induced by Pb(SCN)_(2)while keeping the enlarged grains.The distribution of Rb suggested that the Rb ions are kept isolated with the perovskite grains during the crystallization and Ostwald ripening processes,which contributes to the formation of the large-grain WBG perovskite film with minimum non-radiative recombination.As a result,a power conversion efficiency(PCE)of 23.0%was achieved on small-area WBG PSCs,while mini-modules with an aperture area of 10.5 cm^(2)exhibited a PCE of 20.2%,among the highest reported for solar cells prepared with WBG perovskites via blade coating.This work presents a scalable and reproducible fabrication strategy for stable MA-free WBG PSCs under ambient conditions,advancing their path toward commercialization.展开更多
Perovskite solar cells(PSCs),which utilize a hybrid organic–inorganic lead halide perovskite as the light-absorbing semiconductor,have emerged as a highly promising photovoltaic technology over the past decade[1−5].
All-perovskite tandem solar cells(TSCs)consist of a wide-bandgap(WBG,1.75-1.8 eV)top subcell and a low-bandgap(LBG,1.2-1.3 eV)bottom subcell,exhibit superior power conversion efficiencies(PCEs)compared to single-junct...All-perovskite tandem solar cells(TSCs)consist of a wide-bandgap(WBG,1.75-1.8 eV)top subcell and a low-bandgap(LBG,1.2-1.3 eV)bottom subcell,exhibit superior power conversion efficiencies(PCEs)compared to single-junction perovskite solar cells(PSCs).In addition,the advantages of lowtemperature solution preparation and low manufactu ring cost make the all-perovskite tandem solar cells widely concerned,and are considered to be one of the most potential next-generation high-performance thin film photovoltaic technologies.In this perspective,we briefly summarize the state-of-the-art advances in monolithic all-perovskite TSCs focusing on the following aspects:LBG perovskite bottom subcells,WBG perovskite top subcells,and interconnecting layers(ICLs).We then discuss the primary strategies to improve their performa nce and finally highlight the perspective regarding the achievement of efficient and stable all-perovskite tandems.展开更多
Achieving high-quality perovskite films without surface defects is regarded as a crucial target for the development of durable high-performance perovskite solar cells.Additive engineering is commonly employed to simul...Achieving high-quality perovskite films without surface defects is regarded as a crucial target for the development of durable high-performance perovskite solar cells.Additive engineering is commonly employed to simultaneously control the growth of perovskite crystals and passivate defects.Here,4-(trifluoromethyl)benzoic anhydride(4-TBA)composed of benzene rings functionalized with carbonyl and trifluoromethyl groups was used as an example additive to study the characteristics of additives used for producing high-quality perovskites and controlling their surface properties.The interaction between4-TBA and perovskite precursor materials was investigated using density functional theory(DFT)simulations.The electron-rich carbonyl group efficiently passivated the under-coordinated lead-ion defects.Additionally,hydrogen bonding between trifluoromethyl and organic cations prevents the generation of cation vacancies.Because of its intrinsic hydrophobicity,the trifluoromethyl group simultaneously improves the moisture and heat stability of the film.4-TBA serves as a universal modifier for various perovskite compositions.The power conversion efficiency(PCE)of inverted perovskite solar cells(PSCs)based on methylammonium(MA)with 4-TBA was improved from 16.15%to 19.28%.Similarly,the PCE of inverted PSCs based on a cesium formamidinium MA(CsFAMA)perovskite film increased from20.72%to 23.58%,upon addition of 4-TBA.Furthermore,the moisture and thermal stability of 4-TBAtreated films and devices was significantly enhanced,along with prolonged device performance.Our work provides guidance on selecting the structure and functional groups that are essential for surface defect passivation and the production of high-quality perovskites.展开更多
Quasi-two-dimensional(2D)perovskite embodies characteristics of both three-dimensional(3D)and 2D perovskites,achieving the superior external environment stability structure of 2D perovskites alongside the high efficie...Quasi-two-dimensional(2D)perovskite embodies characteristics of both three-dimensional(3D)and 2D perovskites,achieving the superior external environment stability structure of 2D perovskites alongside the high efficiency of 3D perovskites.This effect is realized through critical structural modifications in device fabrication.Typically,perovskites have an octahedral structure,generally ABX3,where an organic ammonium cation(A’)participates in forming the perovskite structure,with A’_(n)(n=1 or 2)sandwiched between A_(n-1)B_(n)X_(3n+1)perovskite layers.Depending on whether A’is a monovalent or divalent cation,2D perovskites are classified into Ruddlesden-Popper perovskite or Dion-Jacobson perovskite,each generating different structures.Although each structure achieves similar effects,they incorporate distinct mechanisms in their formation.And according to these different structures,various properties appear,and additive and optimizing methods to increase the efficiency of 3D perovskites also exist in 2D perovskites.In this review,scientific understanding and engineering perspectives of the quasi-2D perovskite is investigated,and the optimal structure quasi-2D and the device optimization is also discussed to provide the insight in the field.展开更多
基金supported by the National Key Research and Development Programs-Intergovernmental International Cooperation in Science and Technology Innovation Project(Grant No.2022YFE0118400)the Natural Science Foundation of Hunan Province(2023JJ50132)+1 种基金Shenzhen Science and Technology Innovation Committee(Grants Nos.JCYJ20220818100211025,and KCXST20221021111616039)Shenzhen Science and Technology Program(No.20231128110928003)。
文摘The introduction of two-dimensional(2D)perovskite layers on top of three-dimensional(3D)perovskite films enhances the performance and stability of perovskite solar cells(PSCs).However,the electronic effect of the spacer cation and the quality of the 2D capping layer are critical factors in achieving the required results.In this study,we compared two fluorinated salts:4-(trifluoromethyl)benzamidine hydrochloride(4TF-BA·HCl)and 4-fluorobenzamidine hydrochloride(4F-BA·HCl)to engineer the 3D/2D perovskite films.Surprisingly,4F-BA formed a high-performance 3D/2D heterojunction,while4TF-BA produced an amorphous layer on the perovskite films.Our findings indicate that the balanced intramolecular charge polarization,which leads to effective hydrogen bonding,is more favorable in 4F-BA than in 4TF-BA,promoting the formation of a crystalline 2D perovskite.Nevertheless,4TF-BA managed to improve efficiency to 24%,surpassing the control device,primarily due to the natural passivation capabilities of benzamidine.Interestingly,the devices based on 4F-BA demonstrated an efficiency exceeding 25%with greater longevity under various storage conditions compared to 4TF-BA-based and the control devices.
基金financially supported by the National Natural Science Foundation of China (52462032, 62274018, 52462031)Natural Science Foundation of Yunnan Province (202501AT070353, 202101BE070001-049)+2 种基金the Xinjiang Construction Corps Key Areas of Science and Technology Research Project (2023AB029)the Tianchi Talent Program of Xinjiang Uygur Autonomous Region (2024, Jiangzhao Chen)the Key Project of Chongqing Overseas Students Returning to China Entrepreneurship and Innovation Support Plan (cx2023006)。
文摘In recent years, the research advancements have high-lighted the critical role of the A-site cation in determining the optoelectronic and physicochemical properties of organicinorganic lead halide perovskites. Mixed-cation perovskites(MCPs) have been extensively used as absorber thin films in perovskite solar cells(PSCs), achieving high power conversion efficiencies(PCE) over 26%^([1, 2]).
基金support from National Key Research and Development Program of China(2024YFE0217100)the National Natural Science Foundation of China(21905006,22261160370,and 62105075)+7 种基金the Guangdong Provincial Science and Technology Plan(2021A0505110003)the Natural Science Foundation of Hunan Province,China(2023JJ50132)Guangxi Department of Science and Technology(2020GXNSFBA159049 and AD19110030)the Shenzhen Science and Technology Program(SGDX20230116093205009,JCYJ20220818100211025 and 2022378670)the Natural Science Foundation of Top Talent of SZTU(GDRC202343)financial support of Innovation and Technology Fund(#GHP/245/22SZ)The University Grant Council of the University of Hong Kong(grant No.2302101786)General Research Fund(grant Nos.17200823 and 17310624)from the Research Grants Council.
文摘Halide perovskites have emerged as promising materials for X-ray detection with exceptional properties and reasonable costs.Among them,heterostructures between 3D perovskites and low-dimensional perovskites attract intensive studies of their advantages due to low-level ion migration and decent stability.However,there is still a lack of methods to precisely construct heterostructures and a fundamental understanding of their structure-dependent optoelectronic properties.Herein,a gas-phase method was developed to grow 2D perovskites directly on 3D perovskites with nanoscale accuracy.In addition,the larger steric hindrance of organic layers of 2D perovskites was proved to enable slower ion migration,which resulted in reduced trap states and better stability.Based on MAPbBr_(3)single crystals with the(PA)_(2)PbBr_(4)capping layer,the X-ray detector achieved a sensitivity of 22,245μC Gy_(air)^(−1)cm^(−2),a response speed of 240μs,and a dark current drift of 1.17.10^(–4)nA cm^(−1)s^(−1)V^(−1),which were among the highest reported for state-of-the-art perovskite-based X-ray detectors.This study presents a precise synthesis method to construct perovskite-based heterostructures.It also brings an in-depth understanding of the relationship between lattice structures and properties,which are beneficial for advancing high-performance and cost-effective X-ray detectors.
基金the financial support from the National Key R&D Program of China(2021YFF0500500)the National Natural Science Foundation of China(62474131,62274132,and 62204189)。
文摘Ambient-air,moisture-assisted annealing is widely used in fabricating perovskite solar cells(PSCs).However,the inherent sensitivity of perovskite intermediate-phase to moisture—due to fast and spontaneous intermolecular exchange reaction—requires strict control of ambient humidity and immediate thermal annealing treatment,raising manufacturing costs and causing fast nucleation of perovskite films.We report herein a self-buffered molecular migration strategy to slow down the intermolecular exchange reaction by introducing a n-butylammonium bromide shielding layer,which limits moisture diffusion into intermediate-phase film.This further endows the notably wide nucleation time and humidity windows for perovskite crystallization in ambient air.Consequently,the optimized 1.68 e V-bandgap n-i-p structured PSC reaches a record-high reverse-scan(RS)PCE of 22.09%.Furthermore,the versatility and applicability of as-proposed self-buffered molecular migration strategy are certified by employing various shielding materials and 1.53 eV-/1.77 eV-bandgap perovskite materials.The n-i-p structured PSCs based on 1.53 eV-and 1.77 eV-bandgap perovskite films achieve outstanding RS PCEs of 25.23%and 19.09%,respectively,both of which are beyond of the state-of-the-art ambient-air processed PSCs.
基金financially supported by National Natural Science Foundation of China(No.22302155)the Fundamental Research Funds of the Center Universities(No.D5000240188)the research program of ZJUT(YJY-ZS-20240001)。
文摘Metal halide perovskites(MHPs)with striking electrical and optical properties have appeared at the forefront of semiconductor materials for photocatalytic redox reactions but still suffer from some intrinsic drawbacks such as inferior stability,severe charge-carrier recombination,and limited active sites.Heterojunctions have recently been widely constructed to improve light absorption,passivate surface for enhanced stability,and promote charge-carrier dynamics of MHPs.However,little attention has been paid to the review of MHPs-based heterojunctions for photocatalytic redox reactions.Here,recent advances of MHPs-based heterojunctions for photocatalytic redox reactions are highlighted.The structure,synthesis,and photophysical properties of MHPs-based heterojunctions are first introduced,including basic principles,categories(such as Schottky junction,type-I,type-II,Z-scheme,and S-scheme junction),and synthesis strategies.MHPs-based heterojunctions for photocatalytic redox reactions are then reviewed in four categories:H2evolution,CO_(2)reduction,pollutant degradation,and organic synthesis.The challenges and prospects in solar-light-driven redox reactions with MHPs-based heterojunctions in the future are finally discussed.
基金the National Natural Science Foundation of China(Nos.62374029,22175029,62474033,and W2433038)the Young Elite Scientists Sponsorship Program by CAST(No.YESS20220550)+2 种基金the Sichuan Science and Technology Program(No.2024NSFSC0250)the Natural Science Foundation of Shenzhen Innovation Committee(JCYJ20210324135614040)the Fundamental Research Funds for the Central Universities of China(No.ZYGX2022J032).
文摘Perovskite solar cells(PSCs)have emerged as promising photovoltaic technologies owing to their remarkable power conversion efficiency(PCE).However,heat accumulation under continuous illumination remains a critical bottleneck,severely affecting device stability and long-term operational performance.Herein,we present a multifunctional strategy by incorporating highly thermally conductive Ti_(3)C_(2)T_(X) MXene nanosheets into the perovskite layer to simultaneously enhance thermal management and optoelectronic properties.The Ti_(3)C_(2)T_(X) nanosheets,embedded at perovskite grain boundaries,construct efficient thermal conduction pathways,significantly improving the thermal conductivity and diffusivity of the film.This leads to a notable reduction in the device’s steady-state operating temperature from 42.96 to 39.97 under 100 mW cm^(−2) illumination,thereby alleviating heat-induced performance degradation.Beyond thermal regulation,Ti_(3)C_(2)T_(X),with high conductivity and negatively charged surface terminations,also serves as an effective defect passivation agent,reducing trap-assisted recombination,while simultaneously facilitating charge extraction and transport by optimizing interfacial energy alignment.As a result,the Ti_(3)C_(2)T_(X)-modified PSC achieve a champion PCE of 25.13%and exhibit outstanding thermal stability,retaining 80%of the initial PCE after 500 h of thermal aging at 85 and 30±5%relative humidity.(In contrast,control PSC retain only 58%after 200 h.)Moreover,under continuous maximum power point tracking in N2 atmosphere,Ti_(3)C_(2)T_(X)-modified PSC retained 70%of the initial PCE after 500 h,whereas the control PSC drop sharply to 20%.These findings highlight the synergistic role of Ti_(3)C_(2)T_(X) in thermal management and optoelectronic performance,paving the way for the development of high-efficiency and heat-resistant perovskite photovoltaics.
基金supported by the National Natural Science Foundation of China under Grants 62404185the industry-academia joint laboratory collaboration between Hiking PV and Xiamen University(20243160C0010)J.Z.is supported by Nanqiang Outstanding Young Talents Program X2450215 of Xiamen University.
文摘Crystalline silicon(c-Si)solar cells,though dominating the photovoltaic market,are nearing their theoretical power conversion efficiencies(PCE)limit of 29.4%,necessitating the adoption of multi-junction technology to achieve higher performance.Among these,perovskiteon-silicon-based multi-junction solar cells have emerged as a promising alternative,where the perovskite offering tunable bandgaps,superior optoelectronic properties,and cost-effective manufacturing.Recent announced double-junction solar cells(PSDJSCs)have achieved the PCE of 34.85%,surpassing all other double-junction technologies.Encouragingly,the rapid advancements in PSDJSCs have spurred increased research interest in perovskite/perovskite/silicon triple-junction solar cells(PSTJSCs)in 2024.This triple-junction solar cell configuration demonstrates immense potential due to their optimum balance between achieving a high PCE limit and managing device complexity.This review provides a comprehensive analysis of PSTJSCs,covering fundamental principles,and technological milestones.Current challenges,including current mismatch,open-circuit voltage deficits,phase segregation,and stability issues,and their corresponding strategies are also discussed,alongside future directions to achieve long-term stability and high PCE.This work aims to advance the understanding of the development in PSTJSCs,paving the way for their practical implementation.
基金supports from the National Natural Science Foundation of China(22375220,U2001214,22471302)the Guangdong Basic and Applied Basic Research Foundation(2024B1515020101)Open Project Fund from State Key Laboratory of Optoelectronic Materials and Technologies(OEMT-2024-KF-08).
文摘Formamidinium lead iodide(FAPbI_(3))perovskite exhibits an impressive X-ray absorption coefficient and a large carrier mobility-lifetime product(μτ),making it as a highly promising candidate for X-ray detection application.However,the presence of larger FA^(+)cation induces to an expansion of the Pb-I octahedral framework,which unfortunately affects both the stability and charge carrier mobility of the corresponding devices.To address this challenge,we develop a novel low-dimensional(HtrzT)PbI_(3) perovskite featuring a conjugated organic cation(1H-1,2,4-Triazole-3-thiol,HtrzT^(+))which matches well with theα-FAPbI_(3) lattices in two-dimensional plane.Benefiting from the matched lattice between(HtrzT)PbI_(3) andα-FAPbI_(3),the anchored lattice enhances the Pb-I bond strength and effectively mitigates the inherent tensile strain of theα-FAPbI_(3) crystal lattice.The X-ray detector based on(HtrzT)PbI_(3)(1.0)/FAPbI_(3) device achieves a remarkable sensitivity up to 1.83×10^(5)μC Gy_(air)^(−1) cm^(−2),along with a low detection limit of 27.6 nGy_(air) s^(−1),attributed to the release of residual stress,and the enhancement in carrier mobility-lifetime product.Furthermore,the detector exhibits outstanding stability under X-ray irradiation with tolerating doses equivalent to nearly 1.17×10^(6) chest imaging doses.
基金supported by grants from the National Natural Science Foundation of China(Grant Nos.22334007).
文摘Perovskite solar cells have achieved remarkable progress in photovoltaic efficiency.However,interfacial defects at the buried and upper interfaces of perovskite layer remain a critical challenge,leading to charge recombination,ion migration,and iodine oxidation.To address this,we propose a novel all-in-one modification strategy employing ammonia borane(BNH6)as a multifunctional complex.By incorporating BNH6 at both buried and upper interfaces simultaneously,we achieve dualinterfacial defect passivation and iodide oxidation suppression through three key mechanisms:(1)hydrolysis-induced interaction with SnO_(2),(2)coordination with Pb^(2+),and(3)inhibition of I−oxidation.This approach significantly enhances device performance,yielding a champion power conversion efficiency(PCE)of 26.43%(certified 25.98%).Furthermore,the unencapsulated device demonstrates prominent enhanced operation stability,maintaining 90%of its initial PCE after 500 h under continuous illumination.Notably,our strategy eliminates the need for separate interface treatments,streamlining fabrication and offering a scalable route toward high-performance perovskite photovoltaics.
基金supported by the NSFC under Grant No.62474169the National Key Research and Development Program of China under Grant No.2024YFB3212200the funding from USTC under Grant Nos.WK2100000025,KY2190000003,and KY2190000006。
文摘Soft X-ray detectors play a vital role in materials science,high-energy physics and medical imaging.Cs_(2)AgBiBr_(6),a lead-free double perovskite,has gained attention for its excellent optoelectronic properties,stability,and nontoxicity.However,its fast crystallization and requirement for high-temperature annealing(>250℃)often lead to inferior film quality,limiting its application in flexible devices.This study introduces an alloying strategy that significantly improves the quality of Cs_(2)AgBiBr_(6)thin films annealed at a reduced temperature of 150℃.Devices based on the alloyed thin films exhibit an ultra-low dark current of 0.32 nA·cm^(-2)and a quantum efficiency of 725%.Furthermore,the first successful integration of Cs_(2)AgBiBr_(6)with a thinfilm transistor backplane demonstrates its superior imaging performance,indicating that Cs_(2)AgBiBr_(6)is a promising material for next-generation soft X-ray sensors.
基金funding from FCT(Fundagao para a Ciencia e Tecnologia,I.P.)under the projects LA/P/0037/2020,UIDP/50025/2020 and UIDB/50025/2020 of the Associate Laboratory Institute of Nanostructures,Nanomodelling and Nanofabrication-i3Nby the projects FlexSolar(PTDC/CTM-REF/1008/2020),and SpaceFlex(2022.01610.PTDC,DOI:10.54499/2022.01610.PTDC)+1 种基金supported by the project M-ECO2-Industrial Cluster for advanced biofuel production,Ref.C644930471-00000041,R2U Technologies and Befunding from the European Union via the project X-STREAM(Horizon EU,ERC CoG,No 101124803)the support of a fellowship from the"la Caixa"Foundation(ID 100010434)。
文摘Low-dimensional(LD)halide perovskites have attracted considerable attention due to their distinctive structures and exceptional optoelectronic properties,including high absorption coefficients,extended charge carrier diffusion lengths,suppressed non-radiative recombination rates,and intense photoluminescence.A key advantage of LD perovskites is the tunability of their optical and electronic properties through the precise optimization of their structural arrangements and dimensionality.This review systematically examines recent progress in the synthesis and optoelectronic characterizations of LD perovskites,focusing on their structural,optical,and photophysical properties that underpin their versatility in diverse applications.The review further summarizes advancements in LD perovskite-based devices,including resistive memory,artificial synapses,photodetectors,light-emitting diodes,and solar cells.Finally,the challenges associated with stability,scalability,and integration,as well as future prospects,are discussed,emphasizing the potential of LD perovskites to drive breakthroughs in device efficiency and industrial applicability.
基金financially supported by the National Natural Science Foundation of China(22379044,22472053)the Science and Technology Commission of Shanghai Municipality(23520710700)+6 种基金the Key Program of the National Natural Science Foundation of China(22239001)the Shanghai Pilot Program for Basic Research(22TQ1400100-5)the ShanghaiMunicipal Natural Science Foundation(25ZR1401081)the Fundamental Research Funds for the Central Universities(JKD01251505,JKVD1251041)the Postdoctoral Fellowship Program of CPSF(GZC20250071)the Shanghai Engineering Research Center of Hierarchical Nanomaterials(18DZ2252400)the Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism(Shanghai Municipal Education Commission)。
文摘The solution processibility of perovskites provides a costeffective and high-throughput route for fabricating state-of-the-art solar cells.However,the fast kinetics of precursor-to-perovskite transformation is susceptible to processing conditions,resulting in an uncontrollable variance in device performance.Here,we demonstrate a supramolecule confined approach to reproducibly fabricate perovskite films with an ultrasmooth,electronically homogeneous surface.The assembly of a calixarene capping layer on precursor surface can induce host-vip interactions with solvent molecules to tailor the desolvation kinetics,and initiate the perovskite crystallization from the sharp molecule-precursor interface.These combined effects significantly reduced the spatial variance and extended the processing window of perovskite films.As a result,the standard efficiency deviations of device-to-device and batch-to-batch devices were reduced from 0.64-0.26%to 0.67-0.23%,respectively.In addition,the perovskite films with ultrasmooth top surfaces exhibited photoluminescence quantum yield>10%and surface recombination velocities<100 cm s^(-1)for both interfaces that yielded p-i-n structured solar cells with power conversion efficiency over 25%.
基金supported by the Foundation of Yunnan Province(Nos.202301AU070021,202201BE070001-027)the Test Foundation of KUST(No.2022T20210208).
文摘Halide perovskite materials have received considerable attention for solar cells,LEDs,lasers etc.owing to their controllable physicochemical properties and structural advantages.However,little research has focused on energy storage and conversion applications,such as use as anodes in lithium-ion batteries.In this paper,all-inorganic lead-free halide perovskite Cs_(3)Bi_(2)Cl_(9)powders were synthesized by the grinding method,and the lattice was successfully adjusted via introducing Mn^(2+).The characterization results show that Mn-ion substitution can cause local lattice distortion to restructure the lattice,which will cause a mixed arrangement of[BiCl_(6)]octahedra to improve the performance of the anode material.This new material can provide a feasible solution for solving the problem of low specific capacity anode materials caused by unstable crystal structures,and also indicates that such perovskites with unique crystal structures and lattice tunability have broad application prospects in lithium-ion batteries.
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supported by the Science,Technology,Innovation Commission of Shenzhen Municipality(GJHZ20220913143204008)Postdoctoral Research Project Funding in Shaanxi Province.
文摘The rapid advancement of metal halide perovskites can be attributed to their exceptional optoelectronic properties and facile solution processing technique.Noteworthy strides have been achieved in the realm of perovskite solar cells(PSCs),with a certified power conversion efficiency(PCE)escalating to 26.7%over the course of a decade,positioning them as promising contenders for next-generation photovoltaic technologies[1].However,the formation of crystal defects,including anion/cation vacancies,Pb–I antisite defects,and uncoordinated Pb^(2+),along the surface and grain boundaries(GBs)of perovskite layers during the solution processing stage poses a significant challenge,compromising the photoelectric performance and stability of PSCs.
基金supported by the National Natural Science Foundation of China(No.62204211)the Australian Research Council(ARC)Discovery Early Career Researcher Award Fellowship(DE230100163)+1 种基金support of the Henry Royce Institute for Advanced Materials through the Industrial Collaboration Programme and MATcelerateZero(EPSRC Grant EP/X527257/1)support for the NEXTCCUS project(Project ID:327327)from the Department for Energy Security and Net Zero,the ACT program,and Horizon 2020(Project No.691712).
文摘Scalable fabrication of efficient wide-bandgap(WBG)perovskite solar cells(PSCs)is crucial to realize the full commercial potential of tandem solar cells.However,there are challenges in fabricating efficient methylammonium-free(MA-free)WBG PSCs by blade coating,especially its phase separation and films stability.In this work,an MA-free WBG perovskite ink is developed for preparing FA_(0.8)Cs_(0.2)Pb(I_(0.75)Br_(0.25))_(3)films by blade coating in ambient air.Among various A-site iodides,RbI is found to be the most effective in suppressing the precipitation of PbI_(2)induced by Pb(SCN)_(2)while keeping the enlarged grains.The distribution of Rb suggested that the Rb ions are kept isolated with the perovskite grains during the crystallization and Ostwald ripening processes,which contributes to the formation of the large-grain WBG perovskite film with minimum non-radiative recombination.As a result,a power conversion efficiency(PCE)of 23.0%was achieved on small-area WBG PSCs,while mini-modules with an aperture area of 10.5 cm^(2)exhibited a PCE of 20.2%,among the highest reported for solar cells prepared with WBG perovskites via blade coating.This work presents a scalable and reproducible fabrication strategy for stable MA-free WBG PSCs under ambient conditions,advancing their path toward commercialization.
文摘Perovskite solar cells(PSCs),which utilize a hybrid organic–inorganic lead halide perovskite as the light-absorbing semiconductor,have emerged as a highly promising photovoltaic technology over the past decade[1−5].
基金financially supported by the National Key R&D Program of China(no.2022YFB4200303)the National Natural Science Foundation of China(no.62174112)+2 种基金the Engineering Featured Team Fund of Sichuan University(no.2020SCUNG102)the Technical Application-Oriented Research Projects for Liaoning Provincial College of Communications(no.xyfzx202305)the Basic Research Projects for the Educational Department of Liaoning Province(LJ212411500014)。
文摘All-perovskite tandem solar cells(TSCs)consist of a wide-bandgap(WBG,1.75-1.8 eV)top subcell and a low-bandgap(LBG,1.2-1.3 eV)bottom subcell,exhibit superior power conversion efficiencies(PCEs)compared to single-junction perovskite solar cells(PSCs).In addition,the advantages of lowtemperature solution preparation and low manufactu ring cost make the all-perovskite tandem solar cells widely concerned,and are considered to be one of the most potential next-generation high-performance thin film photovoltaic technologies.In this perspective,we briefly summarize the state-of-the-art advances in monolithic all-perovskite TSCs focusing on the following aspects:LBG perovskite bottom subcells,WBG perovskite top subcells,and interconnecting layers(ICLs).We then discuss the primary strategies to improve their performa nce and finally highlight the perspective regarding the achievement of efficient and stable all-perovskite tandems.
基金supported by a Research Grant of Pukyong National University(2023)。
文摘Achieving high-quality perovskite films without surface defects is regarded as a crucial target for the development of durable high-performance perovskite solar cells.Additive engineering is commonly employed to simultaneously control the growth of perovskite crystals and passivate defects.Here,4-(trifluoromethyl)benzoic anhydride(4-TBA)composed of benzene rings functionalized with carbonyl and trifluoromethyl groups was used as an example additive to study the characteristics of additives used for producing high-quality perovskites and controlling their surface properties.The interaction between4-TBA and perovskite precursor materials was investigated using density functional theory(DFT)simulations.The electron-rich carbonyl group efficiently passivated the under-coordinated lead-ion defects.Additionally,hydrogen bonding between trifluoromethyl and organic cations prevents the generation of cation vacancies.Because of its intrinsic hydrophobicity,the trifluoromethyl group simultaneously improves the moisture and heat stability of the film.4-TBA serves as a universal modifier for various perovskite compositions.The power conversion efficiency(PCE)of inverted perovskite solar cells(PSCs)based on methylammonium(MA)with 4-TBA was improved from 16.15%to 19.28%.Similarly,the PCE of inverted PSCs based on a cesium formamidinium MA(CsFAMA)perovskite film increased from20.72%to 23.58%,upon addition of 4-TBA.Furthermore,the moisture and thermal stability of 4-TBAtreated films and devices was significantly enhanced,along with prolonged device performance.Our work provides guidance on selecting the structure and functional groups that are essential for surface defect passivation and the production of high-quality perovskites.
基金the Research Grant of Kwangwoon University in 2024 and the National Research Foundation of Korea(RS-2023-00236572 and RS-2023-00212110)funded by the Korea government(MSIT)the project for Collabo R&D between Industry,University,and Research Institute(RS-2024-00414524)funded by Korea Ministry of SMEs and Startups.
文摘Quasi-two-dimensional(2D)perovskite embodies characteristics of both three-dimensional(3D)and 2D perovskites,achieving the superior external environment stability structure of 2D perovskites alongside the high efficiency of 3D perovskites.This effect is realized through critical structural modifications in device fabrication.Typically,perovskites have an octahedral structure,generally ABX3,where an organic ammonium cation(A’)participates in forming the perovskite structure,with A’_(n)(n=1 or 2)sandwiched between A_(n-1)B_(n)X_(3n+1)perovskite layers.Depending on whether A’is a monovalent or divalent cation,2D perovskites are classified into Ruddlesden-Popper perovskite or Dion-Jacobson perovskite,each generating different structures.Although each structure achieves similar effects,they incorporate distinct mechanisms in their formation.And according to these different structures,various properties appear,and additive and optimizing methods to increase the efficiency of 3D perovskites also exist in 2D perovskites.In this review,scientific understanding and engineering perspectives of the quasi-2D perovskite is investigated,and the optimal structure quasi-2D and the device optimization is also discussed to provide the insight in the field.
