The maximum power conversion efficiencies of the top-emitting,oxide-confined,two-dimensional integrated 2×2 and4×4 vertical-cavity surface-emitting laser（VCSEL） arrays with the oxide-apertures of 6 μm,16 ...The maximum power conversion efficiencies of the top-emitting,oxide-confined,two-dimensional integrated 2×2 and4×4 vertical-cavity surface-emitting laser（VCSEL） arrays with the oxide-apertures of 6 μm,16 μm,19 μm,26 μm,29 μm,36 μm,39 μm,and 46 urn are fabricated and characterized,respectively.The maximum power conversion efficiencies increase rapidly with the augment of oxide-aperture at the beginning and then decrease slowly.A maximum value of27.91%at an oxide-aperture of 18.6 μm is achieved by simulation.The experimental data are well consistent with the simulation results,which are analyzed by utilizing an empirical model.展开更多
All polymer solar cells(all-PSCs)promise mechanically-flexible and morphologically-stable organic photovoltaics and have aroused increased interests very recently.However,due to their disorderly conformation structure...All polymer solar cells(all-PSCs)promise mechanically-flexible and morphologically-stable organic photovoltaics and have aroused increased interests very recently.However,due to their disorderly conformation structures within the photoactive film,inefficient charge generation and carrier transport are observed which lead to inferior photovoltaic performance compared to smaller molecular acceptor-based photovoltaics.Here,by diluting PM6 with a cutting-edge polymeric acceptor PY-IT and diluting PY-IT with PM6 or D18,donor-dominating or acceptor-dominating heterojunctions were prepared.Synchrotron X-ray and multiple spectrometer techniques reveal that the diluted heterojunctions receive increased structural order,translating to enhanced carrier mobility,improved exciton diffusion length,and suppressed non-radiative recombination loss during the power conversion.As the results,the corresponding PM6+1%PY-IT/PY-IT+1%D18 and PM6+1%PY-IT/PY-IT+1%PM6 devices fabricated by layer-by-layer deposition received superior power conversion efficiency(PCE)of 19.4%and 18.8%respectively,along with enhanced operational lifetimes in air,outperforming the PCE of 17.5%in the PM6/PY-IT reference device.展开更多
Organic solar cells （OSCs） have advantages like light-weight, flexibility, colorfulness and solution processability [1 ]. The active layer of OSCs generally contains two organic semiconductors： an electron donor an...Organic solar cells （OSCs） have advantages like light-weight, flexibility, colorfulness and solution processability [1 ]. The active layer of OSCs generally contains two organic semiconductors： an electron donor and an electron acceptor. The donor and acceptor make nanoscale phase separation to allow efficient exciton dissociation and also form a three-dimensional （3D） passage to rapidly transfer free charge carriers to respective electrodes.展开更多
Trap-assisted charge recombination is one of the primary limitationsof restricting the performance of organic solar cells. However, effectivelyreducing the presence of traps in the photoactive layer remains challengin...Trap-assisted charge recombination is one of the primary limitationsof restricting the performance of organic solar cells. However, effectivelyreducing the presence of traps in the photoactive layer remains challenging.Herein, wide bandgap polymer donor PTzBI-dF is demonstrated as an effectivemodulator for enhancing the crystallinity of the bulk heterojunction active layerscomposed of D18 derivatives blended with Y6, leading to dense and orderedmolecular packings, and thus, improves photoluminescence quenching properties.As a result, the photovoltaic devices exhibit reduced trap-assisted charge recombinationlosses, achieving an optimized power conversion efficiency of over 19%.Besides the efficiency enhancement, the devices comprised of PTzBI-dF as athird component simultaneously attain decreased current leakage, improved chargecarrier mobilities, and suppressed bimolecular charge recombination, leading toreduced energy losses. The advanced crystalline structures induced by PTzBI-dFand its characteristics, such as well-aligned energy level, and complementaryabsorption spectra, are ascribed to the promising performance improvements.Our findings suggest that donor phase engineering is a feasible approach to tuning the molecular packings in the active layer, providingguidelines for designing effective morphology modulators for high-performance organic solar cells.展开更多
By using two sections of erbium doped fiber and a fiber optical reflector, a novel, highly efficient L-band amplifier is demonstrated with significantly power-conversion-efficiency enhancement and the gain increasing ...By using two sections of erbium doped fiber and a fiber optical reflector, a novel, highly efficient L-band amplifier is demonstrated with significantly power-conversion-efficiency enhancement and the gain increasing of as much as 13 dB.展开更多
All-small organic solar cells(ASM OSCs)inherit the advantages of the distinct merits of small molecules,such as well-defined structures and less batch-to-batch variation.In comparison with the rapid development of pol...All-small organic solar cells(ASM OSCs)inherit the advantages of the distinct merits of small molecules,such as well-defined structures and less batch-to-batch variation.In comparison with the rapid development of polymer-based OSCs,more efforts are needed to devote to improving the performance of ASM OSCs to close the performance gap between ASM and polymer-based OSCs.Herein,a well-known p-dopant named fluoro-7,7,8,8-tetracyano-p-quinodimethane(FTCNQ)was introduced to a highefficiency system of HD-1:BTP-e C9,and a high power conversion efficiency(PCE)of 17.15%was achieved due to the improved electrical properties as well as better morphology of the active layer,supported by the observed higher fill factor(FF)of 79.45%and suppressed non-radiative recombination loss.Furthermore,combining with the further morphology optimization from solvent additive of 1-iodonaphthalene(IN)in the blend film,the HD-1:BTP-e C9-based device with the synergistic effects of both FTCNQ and IN demonstrates a remarkable PCE of 17.73%(certified as 17.49%),representing the best result of binary ASM OSCs to date.展开更多
The Shockley-Queisser(S-Q)model sets a theoretical limit on the power conversion efficiency(PCE)of single-junction solar cells at around 33%.Recently,a PCE of 50%-60%was achieved for the first time in n-type singlejun...The Shockley-Queisser(S-Q)model sets a theoretical limit on the power conversion efficiency(PCE)of single-junction solar cells at around 33%.Recently,a PCE of 50%-60%was achieved for the first time in n-type singlejunction Si solar cells by inhibiting light conversion to heat at low temperatures.Understanding these new observations opens tremendous opportunities for designing solar cells with even higher PCE to provide efficient and powerful energy sources for cryogenic devices and outer and deep space explorations.展开更多
Radio-photovoltaic cell is a micro nuclear battery for devices operating in extreme environments,which converts the decay energy of a radioisotope into electric energy by using a phosphor and a photovoltaic converter....Radio-photovoltaic cell is a micro nuclear battery for devices operating in extreme environments,which converts the decay energy of a radioisotope into electric energy by using a phosphor and a photovoltaic converter.Many phosphors with high light yield and good environmental stability have been developed,but the performance of radio-photovoltaic cells remains far behind expectations in terms of power density and power conversion efficiency,because of the poor photoelectric conversion efficiency of traditional photovoltaic converters under low-light conditions.This paper reports an radio-photovoltaic cell based on an intrinsically stable formamidinium-cesium perovskite photovoltaic converter exhibiting a wide light wavelength response from 300 to 800 nm,high open-circuit voltage(V_(oc)),and remarkable efficiency at low-light intensity.When a He ions accelerator is adopted as a mimickedαradioisotope source with an equivalent activity of 0.83 mCi cm^(-2),the formamidinium-cesium perovskite radio-photovoltaic cell achieves a V_(oc)of 0.498 V,a short-circuit current(J_(sc))of 423.94 nA cm^(-2),and a remarkable power conversion efficiency of 0.886%,which is 6.6 times that of the Si reference radio-photovoltaic cell,as well as the highest among all radio-photovoltaic cells reported so far.This work provides a theoretical basis for enhancing the performance of radio-photovoltaic cells.展开更多
Perovskite solar cells(PSCs)have emerged as a promising photovoltaic technology because of their high light absorption coefficient,long carrier diffusion distance,and tunable bandgap.However,PSCs face challenges such ...Perovskite solar cells(PSCs)have emerged as a promising photovoltaic technology because of their high light absorption coefficient,long carrier diffusion distance,and tunable bandgap.However,PSCs face challenges such as hysteresis effects and stability issues.In this study,we introduced a novel approach to improve film crystallization by leveraging 4-tert-butylpyridine(TBP)molecules,thereby enhancing the performance and stability of PSCs.Our findings demonstrate the effective removal of PbI_(2)from the perovskite surface through strong coordination with TBP molecules.Additionally,by carefully adjusting the concentration of the TBP solution,we achieved enhanced film crystallinity without disrupting the perovskite structure.The TBP-treated perovskite films exhibit a low defect density,improved crystallinity,and improved carrier lifetime.As a result,the PSCs manufactured with TBP treatment achieve power conversion efficiency(PCE)exceeding 24%.Moreover,we obtained the PCE of 21.39%for the 12.25 cm^(2)module.展开更多
A polymeric nanopore membrane with selective ionic transport has been proposed as a potential device to convert the chemical potential energy in salinity gradients to electrical power. However, its energy conversion e...A polymeric nanopore membrane with selective ionic transport has been proposed as a potential device to convert the chemical potential energy in salinity gradients to electrical power. However, its energy conversion efficiency and power density are often limited due to the challenge in reliably controlling the size of the nanopores with the conventional chemical etching method. Here we report that without chemical etching, polyimide （PI） membranes irradiated with GeV heavy ions have negatively charged nanopores, showing nearly perfect selectivity for cations over anions, and they can generate electrical power from salinity gradients. We further demonstrate that the power generation efficiency of the PI membrane approaches the theoretical limit, and the maximum power density reaches 130m W/m2 with a modified etching method, outperforming the previous energy conversion device that was made of polymeric nanopore membranes.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
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
With the continuous improvement of photovoltaic efficiency in the organic photovoltaic(OPV),interface engineering has emerged as a pivotal issue in their practical deployment.Currently,the robust crystallinity of smal...With the continuous improvement of photovoltaic efficiency in the organic photovoltaic(OPV),interface engineering has emerged as a pivotal issue in their practical deployment.Currently,the robust crystallinity of small molecule electron transport layers(ETLs)and the poor film-forming abilities of conjugated polymer ETLs are a huge obstacle in this field.Herein,an innovative and efficient nonconjugated polymer ETL,namely PNDI-SO,which contains polar cationic segments for solubility and conjugated units for efficient charge transport in stable OPV cells,is reported.Endowed with suitable energy levels and excellent electron extraction capabilities,PNDI-SO-based OPV cells attain a power conversion efficiency(PCE)of 18.54%.Furthermore,compared with conventional OPV cells utilizing PFN-Br or PDINN,PNDI-SO substantially enhances long-term stability under continuous illumination,evidenced by a T80 lifetime(signifying retention of 80% of initial performance)exceeding 1250 h.Notably,through scanning electron microscope,we verified that PNDI-SO achieves a harmonious balance between film-forming ability and charge transport properties for ETL,enabling the blade-coating OPV based on PBDB-TF:BTP-eC9 to achieve a PCE of 17.47%.These results suggest the potential of PNDI-SO as a promising interface material for industrial printing applications in OPV fabrication.展开更多
The recently reported efficient polymerized small-molecule acceptors(PSMAs)usually adopt a regioregular backbone by polymerizing small-molecule acceptors precursors with a low-reactivity 5-brominated 3-(dicyanomethyli...The recently reported efficient polymerized small-molecule acceptors(PSMAs)usually adopt a regioregular backbone by polymerizing small-molecule acceptors precursors with a low-reactivity 5-brominated 3-(dicyanomethylidene)indan-1-one(IC)end group or its derivatives,leading to low molecular weight,and thus reduce active layer mechanical properties.Herein,a series of newly designed chlorinated PSMAs originating from isomeric IC end groups are developed by adjusting chlorinated positions and copolymerized sites on end groups to achieve high molecular weight,favorable intermolecular interaction,and improved physicochemical properties.Compared with regioregular PY2Se-Cl-o and PY2Se-Cl-m,regiorandom PY2Se-Cl-ran has a similar absorption profile,moderate lowest unoccupied molecular orbital level,and favorable intermolecular packing and crystallization properties.Moreover,the binary PM6:PY2Se-Cl-ran blend achieves better ductility with a crack-onset strain of 17.5% and improved power conversion efficiency(PCE)of 16.23% in all-polymer solar cells(all-PSCs)due to the higher molecular weight of PY2Se-Cl-ran and optimized blend morphology,while the ternary PM6:J71:PY2Se-Cl-ran blend offers an impressive PCE approaching 17% and excellent device stability,which are all crucial for potential practical applications of all-PSCs in wearable electronics.To date,the efficiency of 16.86% is the highest value reported for the regiorandom PSMAs-based all-PSCs and is also one of the best values reported for the all-PSCs.Our work provides a new perspective to develop efficient all-PSCs,with all high active layer ductility,impressive PCE,and excellent device stability,towards practical applications.展开更多
Polymer acceptors based on extended fused ring p skeleton has been proven to be promising candidates for all-polymer solar cells(all-PSCs), due to their remarkable improved light absorption than the traditional imide-...Polymer acceptors based on extended fused ring p skeleton has been proven to be promising candidates for all-polymer solar cells(all-PSCs), due to their remarkable improved light absorption than the traditional imide-based polymer acceptors. To expand structural diversity of the polymer acceptors, herein,two polymer acceptors PSF-IDIC and PSi-IDIC with extended fused ring p skeleton are developed by copolymerization of 2,20-((2 Z,20 Z)-((4,4,9,9-tetrahexadecyl-4,9-dihydro-s-indaceno [1,2-b:5,6-b']dithio phene-2,7-diyl)bis(methanylylidene))bis(3-oxo-2,3-dihydro-1 H-indene-2,1-diylidene))dimalononitrile(IDIC-C16) block with sulfur(S) and fluorine(F) functionalized benzodithiophene(BDT) unit and silicon(Si) atom functionalized BDT unit, respectively. Both polymer acceptors exhibit strong light absorption.The PSF-IDIC exhibits similar energy levels and slightly higher absorption coefficient relative to the PSi-IDIC. After blended with the donor polymer PM6, the functional atoms on the polymer acceptors show quite different effect on the device performance. Both of the acceptors deliver a notably high open circuit voltage(V_(OC)) of the devices, but PSi-IDIC achieves higher V OCthan PSF-IDIC. All-PSC based on PM6:PSi-IDIC attains a power conversion efficiency(PCE) of 8.29%, while PM6:PSF-IDIC-based device achieves a much higher PCE of 10.18%, which is one of the highest values for the all-PSCs reported so far. The superior device performance of PM6:PSF-IDIC is attributed to its higher exciton dissociation and charge transport, decreased charge recombination, and optimized morphology than PM6:PSi-IDIC counterpart. These results suggest that optimizing the functional atoms of the side chain provide an effective strategy to develop high performance polymer acceptors for all-PSCs.展开更多
All-inorganic CsPbI_(2)Br perovskite solar cells(PSCs)have received extensive research interests recently.Nevertheless,their low efficiency and poor long-term stability are still obstacles for further commercial appli...All-inorganic CsPbI_(2)Br perovskite solar cells(PSCs)have received extensive research interests recently.Nevertheless,their low efficiency and poor long-term stability are still obstacles for further commercial application.Herein,we demonstrate that high efficiency and exceptional long-term stability are realized by incorporating gadolinium(III)chloride(GdCl_(3))into the CsPbI_(2)Br perovskite film.The incorporation of GdCl_(3) enhances the Goldschmidt tolerance factor of CsPbI_(2)Br perovskite,yielding a dense perovskite film with small grains,thus the a-phase CsPbI_(2)Br is remarkably stabilized.Additionally,it is found that the GdCl_(3)-incorporated perovskite film achieves suppressed charge recombination and appropriate energy level alignment compared with the pristine CsPbI_(2)Br film.The noticeable increment in efficiency from14.01%(control PSC)to 16.24%is achieved for GdCl_(3)-incorporated PSC.Moreover,the nonencapsulated GdCl_(3)-incorporated PSC exhibits excellent environmental and thermal stability,remaining over 91%or90%of the original efficiency after 1200 h aging at 40%relative humidity or 480 h heating at 85℃ in nitrogen glove box respectively.The encapsulated GdCl_(3)-incorporated PSC presents an improved operational stability with over 88%of initial efficiency under maximum power point(MPP)tracking at 45℃ for1000 h.This work presents an effective ion-incorporation approach for boosting efficiency and long-term stability of all-inorganic PSCs.展开更多
CdSe quantum dot sensitized solar cells （QDSCs） modified with graphene quantum dots （GQDs） have been successfully achieved in this work for the first time. Satisfactorily, the optimized photovoltage （Voc） of the...CdSe quantum dot sensitized solar cells （QDSCs） modified with graphene quantum dots （GQDs） have been successfully achieved in this work for the first time. Satisfactorily, the optimized photovoltage （Voc） of the modified QDSCs was approximately 0.04 V higher than that of plain CdSe QDSCs, consequently improving the photovoltaic performance of the resulting QDSCs. Served as a novel coating on the CdSe QD sensitized photoanode, GQDs played a vital role in improving Voc due to the suppressed charge recombination which has been confirmed by electron impedance spectroscopy as well as transient photovoltage decay measure- ments. Moreover, different adsorption sequences, concentration and deposition time of GQDs have also been systematically investigated to boost the power conversion efficiency （PCE） of CdSe QDSCs. After the coating of CdSe with GQDs, the resulting champion CdSe QDSCs exhibited an improved PCE of 6.59% under AM 1.5G full one sun illumination.展开更多
Nanostructured TiO2 with differentiate morphologies has attracted tremendous attention due to its wide band-gap nature as well as outstanding optical and electric properties for solar-driven light-toelectricity conver...Nanostructured TiO2 with differentiate morphologies has attracted tremendous attention due to its wide band-gap nature as well as outstanding optical and electric properties for solar-driven light-toelectricity conversion application. Layered-stacking TiO2 film such as double-layer, tri-layer, quadrupleor quintuplicate-layer, is highly desirable to the design of high-performance semiconductor material photoanodes and the development of advanced photovoltaic devices. In this minireview, we will summarize the recent progress and achievements on proof-of-concept of layered-stacking TiO2 films（LTFs） for solar cells with emphasis on the tailored properties and synergistic functionalization of LTFs, such as optimized sensitizer adsorption, broadened light confinement as well as facilitated electron transport characteristics.Various demonstrations of LTFs photovoltaic systems provide lots of possibilities and flexibilities for more efficient solar energy utilization that a wide variety of TiO2 with distinguished morphologies can be integrated into differently structured photoanodes with synergistic and complementary advantages. This key structure engineering technology will also pave the way for the development of next generation state-ofthe-art electronics and optoelectronics. Finally, from our point of view, we conclude the future research interest and efforts for constructing more efficient LTFs as photoelectrode, which will be highly warranted to advance the solar energy conversion process.展开更多
The application of organic photovoltaic(OPV)cells to drive off-grid microelectronic devices under indoor light has attracted broad attention.As organic semiconductors intrinsically have less ordered intermolecular pac...The application of organic photovoltaic(OPV)cells to drive off-grid microelectronic devices under indoor light has attracted broad attention.As organic semiconductors intrinsically have less ordered intermolecular packing than inorganic materials,the relatively larger energetic disorder is one of the main results that limit the photovoltaic efficiency of the OPV cells at low carrier density.Here,we optimize the alkyl chains of non-fullerene acceptors to get suppressed energetic disorder.We find the optimal acceptor DTz-R1 with the shortest alkyl chain has the strongest crystalline property and lowest energetic disorder.As a result,over 26%efficiency is recorded for the 1 cm^(2) OPV cells under a light-emitting diode illumination of 500 lux.We also fabricate a 100 cm^(2) cell device and get a PCE of 23.0%,which is an outstanding value for large-area OPV cells.These results suggest that modulation of the energetic disorder is of great importance for further improving the efficiency of OPV cells,especially for indoor applications.展开更多
Efficiency enhancement of Cs_(0.1)(CH_(3)NH_(3))_(0.9)PbI_(3) solar cell devices was performed by using iso-butyl ammonium iodide(IBA)passivated on Cs_(0.1)(CH_(3)NH_(3))_(0.9)PbI_(3) films.The n-i-p structure of pero...Efficiency enhancement of Cs_(0.1)(CH_(3)NH_(3))_(0.9)PbI_(3) solar cell devices was performed by using iso-butyl ammonium iodide(IBA)passivated on Cs_(0.1)(CH_(3)NH_(3))_(0.9)PbI_(3) films.The n-i-p structure of perovskite solar cell devices was fabricated with the structure of FTO/SnO_(2)/Cs_(0.1)(CH_(3)NH_(3))_(0.9)PbI_(3)(FTO,i.e.,fluorine doped tin oxide)and IBA/Spiro-OMeTAD/Ag.The effect of different weights of IBA passivated on Cs-doped perovskite solar cells(PSCs)was systematically investigated and compared with non-passivated devices.It was found that the 5-mg IBA-passivated devices exhibited a high power conversion efficiency(PCE)of 15.49%higher than 12.64%of non-IBA-passivated devices.The improvement of photovoltaic parameters of the 5-mg IBA-passivated device can be clearly observed compared to the Cs-doped device.The better performance of the IBA-passivated device can be confirmed by the reduction of PbI_(2) phase in the crystal structure,lower charge recombination rate,lower charge transfer resistance,and improved contact angle of perovskite films.Therefore,IBA passivation on Cs_(0.1)(CH_(3)NH)_(0.9)PbI_(3) is a promising technique to improve the efficiency of Cs-doped perovskite solar cells.展开更多
基金supported by the National Natural Science Foundation of China(Grant Nos.61222501 and 61335004)the Specialized Research Fund for the Doctoral Program of Higher Education of China(Grant No.20111103110019)
文摘The maximum power conversion efficiencies of the top-emitting,oxide-confined,two-dimensional integrated 2×2 and4×4 vertical-cavity surface-emitting laser（VCSEL） arrays with the oxide-apertures of 6 μm,16 μm,19 μm,26 μm,29 μm,36 μm,39 μm,and 46 urn are fabricated and characterized,respectively.The maximum power conversion efficiencies increase rapidly with the augment of oxide-aperture at the beginning and then decrease slowly.A maximum value of27.91%at an oxide-aperture of 18.6 μm is achieved by simulation.The experimental data are well consistent with the simulation results,which are analyzed by utilizing an empirical model.
基金supported by the Key Research and Development Program of Hubei Province(2023BAB116)the National Natural Science Foundation of China(52203238,52273196,52073221)the Fundamental Research Funds for the Central Universities of China(WUT:2021III016JC).
文摘All polymer solar cells(all-PSCs)promise mechanically-flexible and morphologically-stable organic photovoltaics and have aroused increased interests very recently.However,due to their disorderly conformation structures within the photoactive film,inefficient charge generation and carrier transport are observed which lead to inferior photovoltaic performance compared to smaller molecular acceptor-based photovoltaics.Here,by diluting PM6 with a cutting-edge polymeric acceptor PY-IT and diluting PY-IT with PM6 or D18,donor-dominating or acceptor-dominating heterojunctions were prepared.Synchrotron X-ray and multiple spectrometer techniques reveal that the diluted heterojunctions receive increased structural order,translating to enhanced carrier mobility,improved exciton diffusion length,and suppressed non-radiative recombination loss during the power conversion.As the results,the corresponding PM6+1%PY-IT/PY-IT+1%D18 and PM6+1%PY-IT/PY-IT+1%PM6 devices fabricated by layer-by-layer deposition received superior power conversion efficiency(PCE)of 19.4%and 18.8%respectively,along with enhanced operational lifetimes in air,outperforming the PCE of 17.5%in the PM6/PY-IT reference device.
基金supported by the National Natural Science Foundation of China (U1401244, 21374025, 21372053, 21572041, and 51503050)the National Key Research and Development Program of China (2017YFA0206600)+1 种基金State Key Laboratory of Luminescent Materials and Devices (2016-skllmd-05)Youth Association for Promoting Innovation (CAS)
文摘Organic solar cells （OSCs） have advantages like light-weight, flexibility, colorfulness and solution processability [1 ]. The active layer of OSCs generally contains two organic semiconductors： an electron donor and an electron acceptor. The donor and acceptor make nanoscale phase separation to allow efficient exciton dissociation and also form a three-dimensional （3D） passage to rapidly transfer free charge carriers to respective electrodes.
基金support from the National Natural Science Foundation of China(62275057)the Guangxi Natural Science Foundation(2023GXNSFFA026004 and 2022GXNSFDA035066)+2 种基金the Innovation Project of Guangxi Graduate Education(YCBZ2024034)Natural Science Foundation of Ningbo under grant(2022J149)Natural Science Foundation of Ningbo under grant(2022A-230-G)
文摘Trap-assisted charge recombination is one of the primary limitationsof restricting the performance of organic solar cells. However, effectivelyreducing the presence of traps in the photoactive layer remains challenging.Herein, wide bandgap polymer donor PTzBI-dF is demonstrated as an effectivemodulator for enhancing the crystallinity of the bulk heterojunction active layerscomposed of D18 derivatives blended with Y6, leading to dense and orderedmolecular packings, and thus, improves photoluminescence quenching properties.As a result, the photovoltaic devices exhibit reduced trap-assisted charge recombinationlosses, achieving an optimized power conversion efficiency of over 19%.Besides the efficiency enhancement, the devices comprised of PTzBI-dF as athird component simultaneously attain decreased current leakage, improved chargecarrier mobilities, and suppressed bimolecular charge recombination, leading toreduced energy losses. The advanced crystalline structures induced by PTzBI-dFand its characteristics, such as well-aligned energy level, and complementaryabsorption spectra, are ascribed to the promising performance improvements.Our findings suggest that donor phase engineering is a feasible approach to tuning the molecular packings in the active layer, providingguidelines for designing effective morphology modulators for high-performance organic solar cells.
文摘By using two sections of erbium doped fiber and a fiber optical reflector, a novel, highly efficient L-band amplifier is demonstrated with significantly power-conversion-efficiency enhancement and the gain increasing of as much as 13 dB.
基金supported by the Ministry of Science and Technology of the People’s Republic of China(Mo ST,2022YFB4200400,2019YFA0705900)the National Natural Science Foundation of China(21935007,52025033,51873089)+3 种基金Tianjin city(20JCZDJC00740,22JCQNJC00530)111 Project(B12015)the Fundamental Research Funds for the Central Universities,Nankai University(023-ZB22000105,020-ZB22000110,020-92220002)Haihe Laboratory of Sustainable Chemical Transformations。
文摘All-small organic solar cells(ASM OSCs)inherit the advantages of the distinct merits of small molecules,such as well-defined structures and less batch-to-batch variation.In comparison with the rapid development of polymer-based OSCs,more efforts are needed to devote to improving the performance of ASM OSCs to close the performance gap between ASM and polymer-based OSCs.Herein,a well-known p-dopant named fluoro-7,7,8,8-tetracyano-p-quinodimethane(FTCNQ)was introduced to a highefficiency system of HD-1:BTP-e C9,and a high power conversion efficiency(PCE)of 17.15%was achieved due to the improved electrical properties as well as better morphology of the active layer,supported by the observed higher fill factor(FF)of 79.45%and suppressed non-radiative recombination loss.Furthermore,combining with the further morphology optimization from solvent additive of 1-iodonaphthalene(IN)in the blend film,the HD-1:BTP-e C9-based device with the synergistic effects of both FTCNQ and IN demonstrates a remarkable PCE of 17.73%(certified as 17.49%),representing the best result of binary ASM OSCs to date.
基金support from the National Natural Science Foundation of China(Grant Nos.52371197,51671139).
文摘The Shockley-Queisser(S-Q)model sets a theoretical limit on the power conversion efficiency(PCE)of single-junction solar cells at around 33%.Recently,a PCE of 50%-60%was achieved for the first time in n-type singlejunction Si solar cells by inhibiting light conversion to heat at low temperatures.Understanding these new observations opens tremendous opportunities for designing solar cells with even higher PCE to provide efficient and powerful energy sources for cryogenic devices and outer and deep space explorations.
基金the financial support from the National Natural Science Foundation of China(grant numbers 11922507,12050005,52002140)Fundamental Research Funds for the Central Universities(2020kfyXJJS008)+1 种基金Major State Basic Research Development Program of China(2021YFB3201000)Young Elite Scientists Sponsorship Program by CAST
文摘Radio-photovoltaic cell is a micro nuclear battery for devices operating in extreme environments,which converts the decay energy of a radioisotope into electric energy by using a phosphor and a photovoltaic converter.Many phosphors with high light yield and good environmental stability have been developed,but the performance of radio-photovoltaic cells remains far behind expectations in terms of power density and power conversion efficiency,because of the poor photoelectric conversion efficiency of traditional photovoltaic converters under low-light conditions.This paper reports an radio-photovoltaic cell based on an intrinsically stable formamidinium-cesium perovskite photovoltaic converter exhibiting a wide light wavelength response from 300 to 800 nm,high open-circuit voltage(V_(oc)),and remarkable efficiency at low-light intensity.When a He ions accelerator is adopted as a mimickedαradioisotope source with an equivalent activity of 0.83 mCi cm^(-2),the formamidinium-cesium perovskite radio-photovoltaic cell achieves a V_(oc)of 0.498 V,a short-circuit current(J_(sc))of 423.94 nA cm^(-2),and a remarkable power conversion efficiency of 0.886%,which is 6.6 times that of the Si reference radio-photovoltaic cell,as well as the highest among all radio-photovoltaic cells reported so far.This work provides a theoretical basis for enhancing the performance of radio-photovoltaic cells.
基金financial support from various entities,including the Foundation of Anhui Science and Technology University[HCYJ202201]the Anhui Science and Technology University’s Student Innovation and Entrepreneurship Training Program[S202310879115,202310879053]+4 种基金the Key Project of Natural Science Research in Anhui Science and Technology University[2021ZRZD07]the Chuzhou Science and Technology Project[2021GJ002]the Anhui Province Key Research and Development Program[202304a05020085]the Natural Science Research Project of Anhui Educational Committee[2023AH051877]The Opening Project of State Key Laboratory of Advanced Technology for Float Glass[2020KF06,2022KF06]。
文摘Perovskite solar cells(PSCs)have emerged as a promising photovoltaic technology because of their high light absorption coefficient,long carrier diffusion distance,and tunable bandgap.However,PSCs face challenges such as hysteresis effects and stability issues.In this study,we introduced a novel approach to improve film crystallization by leveraging 4-tert-butylpyridine(TBP)molecules,thereby enhancing the performance and stability of PSCs.Our findings demonstrate the effective removal of PbI_(2)from the perovskite surface through strong coordination with TBP molecules.Additionally,by carefully adjusting the concentration of the TBP solution,we achieved enhanced film crystallinity without disrupting the perovskite structure.The TBP-treated perovskite films exhibit a low defect density,improved crystallinity,and improved carrier lifetime.As a result,the PSCs manufactured with TBP treatment achieve power conversion efficiency(PCE)exceeding 24%.Moreover,we obtained the PCE of 21.39%for the 12.25 cm^(2)module.
基金Supported by the National Natural Science Foundation of China under Grant No 11335003
文摘A polymeric nanopore membrane with selective ionic transport has been proposed as a potential device to convert the chemical potential energy in salinity gradients to electrical power. However, its energy conversion efficiency and power density are often limited due to the challenge in reliably controlling the size of the nanopores with the conventional chemical etching method. Here we report that without chemical etching, polyimide （PI） membranes irradiated with GeV heavy ions have negatively charged nanopores, showing nearly perfect selectivity for cations over anions, and they can generate electrical power from salinity gradients. We further demonstrate that the power generation efficiency of the PI membrane approaches the theoretical limit, and the maximum power density reaches 130m W/m2 with a modified etching method, outperforming the previous energy conversion device that was made of polymeric nanopore membranes.
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the National Natural Science Foundation of China(52303218 and 52303222)the China Postdoctoral Science Foundation(2022M720314)+1 种基金the Natural Science Foundation of Fujian Province(2023J01403)the Beijing Postdoctoral Science Foundation(2023-zz-101)for funding。
文摘With the continuous improvement of photovoltaic efficiency in the organic photovoltaic(OPV),interface engineering has emerged as a pivotal issue in their practical deployment.Currently,the robust crystallinity of small molecule electron transport layers(ETLs)and the poor film-forming abilities of conjugated polymer ETLs are a huge obstacle in this field.Herein,an innovative and efficient nonconjugated polymer ETL,namely PNDI-SO,which contains polar cationic segments for solubility and conjugated units for efficient charge transport in stable OPV cells,is reported.Endowed with suitable energy levels and excellent electron extraction capabilities,PNDI-SO-based OPV cells attain a power conversion efficiency(PCE)of 18.54%.Furthermore,compared with conventional OPV cells utilizing PFN-Br or PDINN,PNDI-SO substantially enhances long-term stability under continuous illumination,evidenced by a T80 lifetime(signifying retention of 80% of initial performance)exceeding 1250 h.Notably,through scanning electron microscope,we verified that PNDI-SO achieves a harmonious balance between film-forming ability and charge transport properties for ETL,enabling the blade-coating OPV based on PBDB-TF:BTP-eC9 to achieve a PCE of 17.47%.These results suggest the potential of PNDI-SO as a promising interface material for industrial printing applications in OPV fabrication.
基金National Natural Science Foundation of China,Grant/Award Numbers:21704082,21875182,22005121Key Scientific and Technological Innovation Team Project of Shaanxi Province,Grant/Award Number:2020TD‐002111 project 2.0,Grant/Award Number:BP2018008。
文摘The recently reported efficient polymerized small-molecule acceptors(PSMAs)usually adopt a regioregular backbone by polymerizing small-molecule acceptors precursors with a low-reactivity 5-brominated 3-(dicyanomethylidene)indan-1-one(IC)end group or its derivatives,leading to low molecular weight,and thus reduce active layer mechanical properties.Herein,a series of newly designed chlorinated PSMAs originating from isomeric IC end groups are developed by adjusting chlorinated positions and copolymerized sites on end groups to achieve high molecular weight,favorable intermolecular interaction,and improved physicochemical properties.Compared with regioregular PY2Se-Cl-o and PY2Se-Cl-m,regiorandom PY2Se-Cl-ran has a similar absorption profile,moderate lowest unoccupied molecular orbital level,and favorable intermolecular packing and crystallization properties.Moreover,the binary PM6:PY2Se-Cl-ran blend achieves better ductility with a crack-onset strain of 17.5% and improved power conversion efficiency(PCE)of 16.23% in all-polymer solar cells(all-PSCs)due to the higher molecular weight of PY2Se-Cl-ran and optimized blend morphology,while the ternary PM6:J71:PY2Se-Cl-ran blend offers an impressive PCE approaching 17% and excellent device stability,which are all crucial for potential practical applications of all-PSCs in wearable electronics.To date,the efficiency of 16.86% is the highest value reported for the regiorandom PSMAs-based all-PSCs and is also one of the best values reported for the all-PSCs.Our work provides a new perspective to develop efficient all-PSCs,with all high active layer ductility,impressive PCE,and excellent device stability,towards practical applications.
基金the National Natural Science Foundation of China (NSFC) (51673092, 51973087 and 21762029) for financial support。
文摘Polymer acceptors based on extended fused ring p skeleton has been proven to be promising candidates for all-polymer solar cells(all-PSCs), due to their remarkable improved light absorption than the traditional imide-based polymer acceptors. To expand structural diversity of the polymer acceptors, herein,two polymer acceptors PSF-IDIC and PSi-IDIC with extended fused ring p skeleton are developed by copolymerization of 2,20-((2 Z,20 Z)-((4,4,9,9-tetrahexadecyl-4,9-dihydro-s-indaceno [1,2-b:5,6-b']dithio phene-2,7-diyl)bis(methanylylidene))bis(3-oxo-2,3-dihydro-1 H-indene-2,1-diylidene))dimalononitrile(IDIC-C16) block with sulfur(S) and fluorine(F) functionalized benzodithiophene(BDT) unit and silicon(Si) atom functionalized BDT unit, respectively. Both polymer acceptors exhibit strong light absorption.The PSF-IDIC exhibits similar energy levels and slightly higher absorption coefficient relative to the PSi-IDIC. After blended with the donor polymer PM6, the functional atoms on the polymer acceptors show quite different effect on the device performance. Both of the acceptors deliver a notably high open circuit voltage(V_(OC)) of the devices, but PSi-IDIC achieves higher V OCthan PSF-IDIC. All-PSC based on PM6:PSi-IDIC attains a power conversion efficiency(PCE) of 8.29%, while PM6:PSF-IDIC-based device achieves a much higher PCE of 10.18%, which is one of the highest values for the all-PSCs reported so far. The superior device performance of PM6:PSF-IDIC is attributed to its higher exciton dissociation and charge transport, decreased charge recombination, and optimized morphology than PM6:PSi-IDIC counterpart. These results suggest that optimizing the functional atoms of the side chain provide an effective strategy to develop high performance polymer acceptors for all-PSCs.
基金supported by the National Natural Science Foundation of China(52172237,52072228)the Shaanxi International Cooperational Project(2020KWZ-018)+1 种基金the Research Fund of the State Key Laboratory of Solidification Processing(NPU),China(Grant No.2021-QZ-02)the Fundamental Research Funds for the Central Universities(3102019JC005)。
文摘All-inorganic CsPbI_(2)Br perovskite solar cells(PSCs)have received extensive research interests recently.Nevertheless,their low efficiency and poor long-term stability are still obstacles for further commercial application.Herein,we demonstrate that high efficiency and exceptional long-term stability are realized by incorporating gadolinium(III)chloride(GdCl_(3))into the CsPbI_(2)Br perovskite film.The incorporation of GdCl_(3) enhances the Goldschmidt tolerance factor of CsPbI_(2)Br perovskite,yielding a dense perovskite film with small grains,thus the a-phase CsPbI_(2)Br is remarkably stabilized.Additionally,it is found that the GdCl_(3)-incorporated perovskite film achieves suppressed charge recombination and appropriate energy level alignment compared with the pristine CsPbI_(2)Br film.The noticeable increment in efficiency from14.01%(control PSC)to 16.24%is achieved for GdCl_(3)-incorporated PSC.Moreover,the nonencapsulated GdCl_(3)-incorporated PSC exhibits excellent environmental and thermal stability,remaining over 91%or90%of the original efficiency after 1200 h aging at 40%relative humidity or 480 h heating at 85℃ in nitrogen glove box respectively.The encapsulated GdCl_(3)-incorporated PSC presents an improved operational stability with over 88%of initial efficiency under maximum power point(MPP)tracking at 45℃ for1000 h.This work presents an effective ion-incorporation approach for boosting efficiency and long-term stability of all-inorganic PSCs.
基金supported by the National Natural Science Foundation of China (21175043,91233102)the Fundamental Research Funds for the Central Universities for financial support
文摘CdSe quantum dot sensitized solar cells （QDSCs） modified with graphene quantum dots （GQDs） have been successfully achieved in this work for the first time. Satisfactorily, the optimized photovoltage （Voc） of the modified QDSCs was approximately 0.04 V higher than that of plain CdSe QDSCs, consequently improving the photovoltaic performance of the resulting QDSCs. Served as a novel coating on the CdSe QD sensitized photoanode, GQDs played a vital role in improving Voc due to the suppressed charge recombination which has been confirmed by electron impedance spectroscopy as well as transient photovoltage decay measure- ments. Moreover, different adsorption sequences, concentration and deposition time of GQDs have also been systematically investigated to boost the power conversion efficiency （PCE） of CdSe QDSCs. After the coating of CdSe with GQDs, the resulting champion CdSe QDSCs exhibited an improved PCE of 6.59% under AM 1.5G full one sun illumination.
基金the financial supports from the NSFC(51472274)the GDUPS(2016)+2 种基金the program of Guangzhou Science and Technology Project(201504010031)the NSF of Guangdong Province(S2013030013474)the Fundamental Research Funds for the Central Universities
文摘Nanostructured TiO2 with differentiate morphologies has attracted tremendous attention due to its wide band-gap nature as well as outstanding optical and electric properties for solar-driven light-toelectricity conversion application. Layered-stacking TiO2 film such as double-layer, tri-layer, quadrupleor quintuplicate-layer, is highly desirable to the design of high-performance semiconductor material photoanodes and the development of advanced photovoltaic devices. In this minireview, we will summarize the recent progress and achievements on proof-of-concept of layered-stacking TiO2 films（LTFs） for solar cells with emphasis on the tailored properties and synergistic functionalization of LTFs, such as optimized sensitizer adsorption, broadened light confinement as well as facilitated electron transport characteristics.Various demonstrations of LTFs photovoltaic systems provide lots of possibilities and flexibilities for more efficient solar energy utilization that a wide variety of TiO2 with distinguished morphologies can be integrated into differently structured photoanodes with synergistic and complementary advantages. This key structure engineering technology will also pave the way for the development of next generation state-ofthe-art electronics and optoelectronics. Finally, from our point of view, we conclude the future research interest and efforts for constructing more efficient LTFs as photoelectrode, which will be highly warranted to advance the solar energy conversion process.
基金This work was financially supported by the National Natural Science Foundation of China(Nos.52003275,22075301,22122905 and 52120105005)J.H.Hou was supported by the Key Research Program of the Chinese Academy of Sciences(No.XDPB13)the Bureau of International Cooperation Chinese Academy of Sciences(No.121111KYSB20200043).
文摘The application of organic photovoltaic(OPV)cells to drive off-grid microelectronic devices under indoor light has attracted broad attention.As organic semiconductors intrinsically have less ordered intermolecular packing than inorganic materials,the relatively larger energetic disorder is one of the main results that limit the photovoltaic efficiency of the OPV cells at low carrier density.Here,we optimize the alkyl chains of non-fullerene acceptors to get suppressed energetic disorder.We find the optimal acceptor DTz-R1 with the shortest alkyl chain has the strongest crystalline property and lowest energetic disorder.As a result,over 26%efficiency is recorded for the 1 cm^(2) OPV cells under a light-emitting diode illumination of 500 lux.We also fabricate a 100 cm^(2) cell device and get a PCE of 23.0%,which is an outstanding value for large-area OPV cells.These results suggest that modulation of the energetic disorder is of great importance for further improving the efficiency of OPV cells,especially for indoor applications.
基金financial support from the Development and Promotion of Science and Technology Talent Project(DPST) and Graduate School,Chiang Mai University
文摘Efficiency enhancement of Cs_(0.1)(CH_(3)NH_(3))_(0.9)PbI_(3) solar cell devices was performed by using iso-butyl ammonium iodide(IBA)passivated on Cs_(0.1)(CH_(3)NH_(3))_(0.9)PbI_(3) films.The n-i-p structure of perovskite solar cell devices was fabricated with the structure of FTO/SnO_(2)/Cs_(0.1)(CH_(3)NH_(3))_(0.9)PbI_(3)(FTO,i.e.,fluorine doped tin oxide)and IBA/Spiro-OMeTAD/Ag.The effect of different weights of IBA passivated on Cs-doped perovskite solar cells(PSCs)was systematically investigated and compared with non-passivated devices.It was found that the 5-mg IBA-passivated devices exhibited a high power conversion efficiency(PCE)of 15.49%higher than 12.64%of non-IBA-passivated devices.The improvement of photovoltaic parameters of the 5-mg IBA-passivated device can be clearly observed compared to the Cs-doped device.The better performance of the IBA-passivated device can be confirmed by the reduction of PbI_(2) phase in the crystal structure,lower charge recombination rate,lower charge transfer resistance,and improved contact angle of perovskite films.Therefore,IBA passivation on Cs_(0.1)(CH_(3)NH)_(0.9)PbI_(3) is a promising technique to improve the efficiency of Cs-doped perovskite solar cells.
