ZnO nanorods are passivated with a TiO2 interracial layer and applied in the CH3NH3PbI3 perovskite solar cell, which prepared by the atomic layer deposition method show a positive effect on the tiff factor and power c...ZnO nanorods are passivated with a TiO2 interracial layer and applied in the CH3NH3PbI3 perovskite solar cell, which prepared by the atomic layer deposition method show a positive effect on the tiff factor and power conversion efficiency. With TiO2 interracial passivation, the charge recombination in the ZnO/CH3NH3PbI3 interface is effectively suppressed and the maximum power conversion efficiency is enhanced from 11.9% to 13.4%.展开更多
This paper proposes a new mechanism to explain the performance of thin dye-sensitized solar cells （DSSC）. Near-stoichiometric flower-like Cu2ZnSnS4 （CZTS） microspheres with a high specific surface area was fabri- ...This paper proposes a new mechanism to explain the performance of thin dye-sensitized solar cells （DSSC）. Near-stoichiometric flower-like Cu2ZnSnS4 （CZTS） microspheres with a high specific surface area was fabri- cated for use as the photocathode in a DSSC. To improve the extraction and transfer of electrons, graphene was added to the CZTS. A DSSC with a 10-gin TiO2 pho- toanode layer exhibited a slightly degraded efficiency with a CZTS-graphene photocathode, relative to a Pt counter electrode （CE）. Nevertheless, when the thickness of the TiO2 photoanode was reduced to 2 lam, the efficiency of a DSSC with a CZTS-graphene photocathode was greater than that of a Pt-DSSC. It is speculated that, unlike the Pt CE, a CZTS-graphene photocathode not only collects electrons from an external circuit and catalyzes the reduction of the triiodide ions in the electrolyte, but also utilizes unabsorbed photons to produce photo-excited electrons and suppresses charge recombination, thus enhancing the performance of the cell. The use of narrowband gap p-type semiconductors as photocathodes offers a new means of fabricating thin dye-sensitized solar cells and effectively improving the cell performance.展开更多
This paper deals with the profile measurement of impurity ion temperature and toroidal rotation velocity that can be achieved by using the charge exchange recombination spectrum （CXRS） diagnostics tool built on the ...This paper deals with the profile measurement of impurity ion temperature and toroidal rotation velocity that can be achieved by using the charge exchange recombination spectrum （CXRS） diagnostics tool built on the HL-2A toknmak. By using CXRS, an accurate impurity ion temperature and toroidal plasma rotation velocity profile can be achieved under the condition of neutrM beam injection （NBI） heating. Considering the edge effect of the line of CVI 529.06 nm （n= 8-7）, which contains three lines （active exciting spectral line （ACX）, passivity exciting spectral line （PCX） and electron exciting spectral line （ICE））, and using three Gaussian fitted curves, we obtain the following experimental results： the core ion temperature of HL-2A device is nearly thousands of eV, and the plasma rotation velocity reaches about 104 m· s^-1. At the end of paper, some explanations are presented for the relationship between the curves and the inner physical mechanism.展开更多
Charge exchange recombination spectroscopy （CXRS） based on a diagnostic neutral beam （DNB） installed in the HT-7 tokamak is introduced. DNB can provide a 6 A extracted current at 50 kV for 0.1 s in hydrogen. It ca...Charge exchange recombination spectroscopy （CXRS） based on a diagnostic neutral beam （DNB） installed in the HT-7 tokamak is introduced. DNB can provide a 6 A extracted current at 50 kV for 0.1 s in hydrogen. It can penetrate into the core plasma in HT-7. The CXRS system is designed to observe charge exchange （CX） transitions in the visible spectrum. CX light from the beam is focused onto 10 optical fibers, which view the plasma from -5 cm to 20 cm. The CXRS system can measure the ion temperature as low as 0.1 keV. With CXRS, the local ion temperature profile in HT-7 was obtained for the first time.展开更多
With consideration of the effects of the atomic process and the sight line direction on the charge exchange re-combination spectroscopy （CXRS）, a code used to modify the poloidal CXRS measurement on Tokamak-60 Upgra...With consideration of the effects of the atomic process and the sight line direction on the charge exchange re-combination spectroscopy （CXRS）, a code used to modify the poloidal CXRS measurement on Tokamak-60 Upgrade （JT-60U） in Japan Atomic Energy Research Institute is developed, offering an effective tool to modify the measurement and analyse experimental results further. The results show that the poloidal velocity of ion is overestimated but the ion temperature is underestimated by the poloidal CXRS measurement, and they also indicate that the effect of observation angle on rotation velocity is a dominant one in a core region （r/a 〈 0.65）, whereas in an edge region where the sight line is nearly normal to the neutral beam, the observation angle effect is very small. The difference between the modified velocity and the neoclassical velocity is not larger than the error in measurement. The difference inside the internal transport barrier （ITB） region is 2-3 times larger than that outside the ITB region, and it increases when the effect of excited components in neutral beam is taken into account. The radial electric field profile is affected greatly by the poloidal rotation term, which possibly indicates the correlation between the poloidal rotation and the transport barrier formation.展开更多
Ultrafast charge exchange recombination spectroscopy(UF-CXRS)has been developed on the EAST tokamak(Yingying Li et al 2019 Fusion Eng.Des.146522)to measure fast evolutions of ion temperature and toroidal velocity.Here...Ultrafast charge exchange recombination spectroscopy(UF-CXRS)has been developed on the EAST tokamak(Yingying Li et al 2019 Fusion Eng.Des.146522)to measure fast evolutions of ion temperature and toroidal velocity.Here,we report the preliminary diagnostic measurements after relative sensitivity calibration.The measurement results show a much higher temporal resolution compared with conventional CXRS,benefiting from the usage of a prismcoupled,high-dispersion volume-phase holographic transmission grating and a high quantum efficiency,high-gain detector array.Utilizing the UF-CXRS diagnostic,the fast evolutions of the ion temperature and rotation velocity during a set of high-frequency small-amplitude edgelocalized modes(ELMs)are obtained on the EAST tokamak,which are then compared with the case of large-amplitude ELMs.展开更多
Junctions are an important structure that allows charge separation in solar cells and photocatalysts. Here, we studied the charge transfer at an anatase/rutile TiO2 phase junction using time-resolved photoluminescence...Junctions are an important structure that allows charge separation in solar cells and photocatalysts. Here, we studied the charge transfer at an anatase/rutile TiO2 phase junction using time-resolved photoluminescence spectroscopy. Visible （-S00 nm） and near-infrared （NIR, -830 nm） emissions were monitored to give insight into the photoinduced charges of anatase and rutile in the junction, respectively, New fast photoluminescence decay components appeared in the visible emission of futile-phase dominated TiO2 and in the NIR emission of many mixed phase TiO2samples. The fast decays confirmed that the charge separation occurred at the phase junction. The visible emission intensity from the mixed phase TiO2 increased, revealing that charge transfer from rutile to anatase was the main pathway. The charge separation slowed the microsecond time scale photolumines- cence decay rate for charge carriers in both anatase and rutile. However, the millisecond decay of the charge carriers in anatase TiO2 was accelerated, while there was almost no change in the charge carrier dynamics of rutile TiO2. Thus, charge separation at the anatase/rutile phase junction caused an increase in the charge carrier concentration on a microsecond time scale, because of slower electron-hole recombination. The enhanced photocatalytic activity previously observed at ana- tase/rutile phase junctions is likely caused by the improved charge carrier dynamics we report here. These findings may contribute to the development of improved photocatalytic materials.展开更多
Mixed cation and anion based perovskites solar cells exhibited enhanced stability under outdoor conditions,however,it yielded limited power conversion efficiency when TiO_(2) and Spiro-OMeTAD were employed as electron...Mixed cation and anion based perovskites solar cells exhibited enhanced stability under outdoor conditions,however,it yielded limited power conversion efficiency when TiO_(2) and Spiro-OMeTAD were employed as electron and hole transport layer(ETL/HTL)respectively.The inevitable interfacial recombination of charge carriers at ETL/perovskite and perovskite/HTL interface diminished the efficiency in planar(n-i-p)perovskite solar cells.By employing computational approach for uni-dimensional device simulator,the effect of band offset on charge recombination at both interfaces was investigated.We noted that it acquired cliff structure when the conduction band minimum of the ETL was lower than that of the perovskite,and thus maximized interfacial recombination.However,if the conduction band minimum of ETL is higher than perovskite,a spike structure is formed,which improve the performance of solar cell.An optimum value of conduction band offset allows to reach performance of 25.21%,with an open circuit voltage(VOC)of 1231 mV,a current density JSC of 24.57 mA/cm^(2) and a fill factor of 83.28%.Additionally,we found that beyond the optimum offset value,large spike structure could decrease the performance.With an optimized energy level of Spiro-OMeTAD and the thickness of mixed-perovskite layer performance of 26.56% can be attained.Our results demonstrate a detailed understanding about the energy level tuning between the charge selective layers and perovskite and how the improvement in PV performance can be achieved by adjusting the energy level offset.展开更多
Suppressing the nonradiative recombination in the bulk and surface of perovskite film is highly desired to improve the power conversion efficiency(PCE)and stability of halide perovskite solar cells(PSCs).In this study...Suppressing the nonradiative recombination in the bulk and surface of perovskite film is highly desired to improve the power conversion efficiency(PCE)and stability of halide perovskite solar cells(PSCs).In this study,a benzotriazole derivative(6-chloro-1-hydroxybenzotriazole,Cl-HOBT)is applied to improve the crystallinity and reduce the trap density of methylammonium lead iodide(MAPbI3)perovskite film.Meanwhile,incorporation of Cl-HOBT elongates the photoluminescence carrier lifetime and chargerecombination lifetime,implying the trap-assisted nonradiative recombination is greatly suppressed.Besides,the improved energy level alignment and enhanced built-in potential are conducive to the charge carrier separation and transfer process with Cl-HOBT.Consequently,a PCE of 20.27%and an open-circuit voltage(Voc)of 1.09 V are achieved for the inverted MAPbI3 PSCs,along with an 85%maintaining of the initial PCE under stored at relative humidity of 20%for 500 h.Furthermore,the existence of Cl-HOBT could inhibit the formation of Pb0 defect under prolonged UV illumination to retard the degradation of perovskite film.It is believed that this study paves a novel path for the realization of highefficiency PSCs with UV-stability.展开更多
Crystal defect is well-known to have a significant effect on the photocatalytic performance of semiconductors. Herein, defect-rich and-poor BaSn(OH)6(BSOH-Sn and BSOH-Ba) photocatalysts were synthesized by exchanging ...Crystal defect is well-known to have a significant effect on the photocatalytic performance of semiconductors. Herein, defect-rich and-poor BaSn(OH)6(BSOH-Sn and BSOH-Ba) photocatalysts were synthesized by exchanging the addition order of Ba and Sn. Results show that the defect-poor BSOH-Ba exhibited more efficient toluene degradation under ultraviolet(UV) light, which could attribute to the great suppression of photogenerated electron-hole(e--h+) pairs recombination by tuning the defect concentration. The low defect concentration in BSOH-Ba finally promotes the charge separation efficiency, the generation of reactive oxygen species(ROS), and the photocatalytic toluene degradation reactions. This work not only provides an effective way to inhibit the recombination of photogenerated carriers and improve the photocatalytic performance, but also promotes the understanding of defective perovskite-type hydroxide for more photoreactions.展开更多
Influence of recombination centers’ changes on the form of phase portraits has been studied. It has been shown that the shape of the phase portraits depends on the concentration of semiconductor materials’ recombina...Influence of recombination centers’ changes on the form of phase portraits has been studied. It has been shown that the shape of the phase portraits depends on the concentration of semiconductor materials’ recombination centers.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
Rare earth element-enhanced TiO2 achieves high-efficiency photocatalytic overall water splitting Photocatalytic water splitting is a clean energy technology that uses sunlight to split water into oxygen and hydrogen i...Rare earth element-enhanced TiO2 achieves high-efficiency photocatalytic overall water splitting Photocatalytic water splitting is a clean energy technology that uses sunlight to split water into oxygen and hydrogen in order to produce green hydrogen,a clean fuel,without relying on fossil fuels.The process is driven by a photocatalyst.While titanium dioxide(TiO2)has long been studied as a promising semiconductor for photocatalytic water splitting,its efficiency has been hindered by rapid charge recombination and insufficient charge separation.展开更多
This study investigates the intersystem crossing(ISC)mechanism in donor-acceptor(D-A)type distyryl-BODIPY photosensitizers,including previously reported M1(benzene donor),M2,M3(phenothiazine donors),and newly predicte...This study investigates the intersystem crossing(ISC)mechanism in donor-acceptor(D-A)type distyryl-BODIPY photosensitizers,including previously reported M1(benzene donor),M2,M3(phenothiazine donors),and newly predicted M4(triphenylamine donor),M5-M7(nitrogen-containing aliphatic rings with thiophene donors).Using computational chemistry,we analyzed their geometric configurations,spectral properties,spin-orbit coupling,and electron-hole orbitals.We found that S_(2) is a charge transfer singlet state(^(1)CT),T2is a locally excited triplet state(^(3)LE),and the S_(2)→T_(2)transition is the main ISC pathway in M2-M7,following the ^(1)CT→^(3)LE mechanism.M5-M7 show near-vertical dihedral angles between donor and acceptor in the S_(2) state relative to M2-M4,facilitating charge transfer.The strain energies in the nitrogen-containing rings of M5-M7 affect oxidation potentials and ISC.M5,with the highest strain energy,shows the lowest oxidation potential,smaller△_(ES2-T2),highest SOC,and fastest kisc,making it the most efficient predicted singlet oxygen producer.This research clarifies the structure-performance relationships of near-infrared D-A type distyryl-BODIPY photosensitizers and provides a theoretical foundation for developing heavy-atom-free photosensitizers with tuned fluorescence quantum yield and singlet oxygen quantum yield.展开更多
2,2',7,7'-Tetrakis(N,N-di(4-methoxyphenyl)amino)-9,9'-spirobifluorene(Spiro)is an essential hole-transport material used in perovskite solar cells(PSCs).However,the redox reaction of Spiro and its impact a...2,2',7,7'-Tetrakis(N,N-di(4-methoxyphenyl)amino)-9,9'-spirobifluorene(Spiro)is an essential hole-transport material used in perovskite solar cells(PSCs).However,the redox reaction of Spiro and its impact at the interface with the metal electrode are not yet fully understood.In this study,we introduced a crystalline additive(CA)to regulate the redox process of Spiro and its interface with an Ag electrode.Our findings indicate that CA functions as a molecular scaffold,improving the crystallinity and stability of radicals in Spiro throughout the entire redox reaction.This enhancement increases the hole mobility of Spiro and strengthens the internal electric field,thereby improving hole extraction and transport efficiency at both interfaces.Moreover,the optimized redox reaction of Spiro reduces energy loss at the Ag electrode,significantly boosting the power conversion efficiency to 25.21%.Furthermore,CA mitigates the aggregation of lithium salt and enhances the stability of the device.Our findings contribute to a deeper understanding of hole-transport mechanisms of Spiro and emphasize the importance of reducing energy loss at the Spiro/Ag electrode interface in PSCs.展开更多
Semiconductor-cocatalyst interfacial electron transfer has widely been considered as a fast step occurring on picosecond-microsecond timescale in photocatalytic reaction.However,the formed potential barriers severely ...Semiconductor-cocatalyst interfacial electron transfer has widely been considered as a fast step occurring on picosecond-microsecond timescale in photocatalytic reaction.However,the formed potential barriers severely slow this interfacial electronic process by thermionic emission.Although trap-assisted charge recombination can transfer electrons from semiconductor to cocatalyst and can even be evident under weak illumination,the parallel connection with thermionic emission makes the photocatalytic photon utilization encounter a minimum along the variation of light intensity.By this cognition,the light-intensity-dependent photocatalytic behaviors can be predicted by simulating the photoinduced semiconductor-cocatalyst interfacial electron transfer that mainly determines the reaction rate.We then propose a(photo)electrochemical method to evaluate the time constants for occurring this interfacial electronic process in actual photocatalytic reaction without relying on extremely high photon flux that is required to generate discernible optical signal in common instrumental methods based on ultrafast pulse laser.The evaluated decisecond-second timescale can accurately guide us to develop certain strategies to facilitate this rate-determining step to improve photon utilization.展开更多
Developing photosensitizers suitable for the cobalt electrolyte and understanding the structure-property relationship of organic dyes is warranted for the dye-sensitized solar cells （DSSCs）. The DSSCs incorporating ...Developing photosensitizers suitable for the cobalt electrolyte and understanding the structure-property relationship of organic dyes is warranted for the dye-sensitized solar cells （DSSCs）. The DSSCs incorporating tris（1,10-phenanthroline）eobalt（Ⅱ/Ⅲ）-based redox elec- trolyte and four synthesized organic dyes as photosensitizers are described. The photovoltaic performance of these dyes-sensitized solar cells employing the cobalt redox shuttle and the influences of the w-conjugated spacers of organic dyes upon the photovoltage and photocur- rent of mesoscopic titania solar cells are investigated. It is found that organic dyes with thiophene derivates as linkers are suitable for DSSCs employing cobalt electrolytes. DSSCs sensitized with the as-synthesized dyes in combination with the cobalt redox shuttle yield an overall power conversion efficiency of 6.1% under 100 mW/cm2 AM1.5 G illumination.展开更多
Suppressing nonradiative recombination and releasing residual strain areprerequisites to improving the efficiency and stability of perovskite solar cells(PSCs).Here,long-chain polyacrylic acid(PAA)is used to reinforce...Suppressing nonradiative recombination and releasing residual strain areprerequisites to improving the efficiency and stability of perovskite solar cells(PSCs).Here,long-chain polyacrylic acid(PAA)is used to reinforce SnO_(2)film and passivate SnO_(2)defects,forming a structure similar to“reinforcedconcrete”with high tensile strength and fewer microcracks.Simultaneously,PAA is also introduced to the SnO_(2)/perovskite interface as a“buffer spring”torelease residual strain,which also acts as a“dual-side passivation interlayer”to passivate the oxygen vacancies of SnO_(2)and Pb dangling bonds in halideperovskites.As a result,the best inorganic CsPbBr_(3)PSC achieves a championpower conversion efficiency of 10.83%with an ultrahigh open-circuit voltageof 1.674 V.The unencapsulated PSC shows excellent stability under 80%relative humidity and 80℃over 120 days.展开更多
Tin dioxide(SnO2) is generally regarded as a promising electron-transporting layer(ETL) for state-of-theart perovskite solar cells(PSCs), however, the ubiquitous oxygen-vacancy-related defects at SnO2 surface and the ...Tin dioxide(SnO2) is generally regarded as a promising electron-transporting layer(ETL) for state-of-theart perovskite solar cells(PSCs), however, the ubiquitous oxygen-vacancy-related defects at SnO2 surface and the large energy difference between conduction band of SnO2 and perovskite layer undoubtedly cause severe charge carrier recombination, resulting in sluggish charge extraction efficiency and non-negligible open-circuit voltage(Voc) loss. Herein, a chlorine-containing TiOxCl4-2x accessory layer is fabricated by immersing SnO2 layer into the TiCl4 aqueous solution to passivate the surface oxygen-vacancy-related defects of SnO2 layer and to set an intermediate energy level at ETL/perovskite interface in all-inorganic cesium lead tri-bromine(CsPbBr3) PSCs. Furthermore, the TiOxCl4-2x layer also improves the infiltration of SnO2 layer surface toward perovskite precursor for high-quality perovskite film. Finally, the hole-free, allinorganic CsPbBr3PSC with a structure of FTO/SnO2/TiOxCl4-2x/Cs0.91Rb0.09PbBr3/carbon achieves a champion efficiency of 10.44% with a Vocas high as 1.629 V in comparison to 8.31% for control device. Moreover, the optimized solar cell presents good stability in 80% humidity in air.展开更多
In the present investigation,a new composite nanostructured photoanodes were prepared using TiO_2 nanotubes（TNTs） with TiO_2 nanoparticles（TNPs）.TNPs were synthesized by sol-gel method,and TNTs were prepared throu...In the present investigation,a new composite nanostructured photoanodes were prepared using TiO_2 nanotubes（TNTs） with TiO_2 nanoparticles（TNPs）.TNPs were synthesized by sol-gel method,and TNTs were prepared through alkali hydrothermal method.Dye-sensitized solar cells（DSSCs） were fabricated with different photoanodes comprising of various ratios of TNTs ＋ TNPs,synthetic indigo dye as photosensitizer,PMII（l-propyl-3-methylimidazolium iodide） as ionic liquid electrolyte and cobalt sulfide as counter electrode.The structures and morphologies of TNPs and TNTs were analyzed through X-ray diffractometer,transmission electron microscope and scanning electron microscopes.The results of the investigation showed that the DSSC-4 made with composite photoanode structure（TNTs/TNPs）（90% of TNPs ＋ 10% of TNTs） had improved photocurrent efficiency（2.11%） than pure TNPs（1.00%） and TNT film（0.78%）.Electrochemical impedance spectra revealed that the composite TNTs/TNPs film-based DSSCs possessed the lowest charge-transfer resistances and longest electron lifetime.Hence,it could be concluded that the composite TNTs/TNPs photoanode facilitates the charge transport rate and enhances the efficiencies of DSSCs.展开更多
基金Supported by the National Key Basic Research Program of China under Grant Nos 2012CB932903 and 2012CB932904the Beijing Science and Technology Committee under Grant No Z131100006013003+1 种基金the National Natural Science Foundation of China under Grant Nos 51372270,51372272,21173260,11474333,91433205,51421002 and 91233202the Knowledge Innovation Program of Chinese Academy of Sciences
文摘ZnO nanorods are passivated with a TiO2 interracial layer and applied in the CH3NH3PbI3 perovskite solar cell, which prepared by the atomic layer deposition method show a positive effect on the tiff factor and power conversion efficiency. With TiO2 interracial passivation, the charge recombination in the ZnO/CH3NH3PbI3 interface is effectively suppressed and the maximum power conversion efficiency is enhanced from 11.9% to 13.4%.
基金This work was supported by the National Natural Science Foundation of China （51272033, 51572037 and 51335002）, the Priority Academic Program Development of Jiangsu Higher Education Institutions and the Natural Science Foundation of the Jiangsu Higher Education Institutions of China （14KJA430001）.
文摘This paper proposes a new mechanism to explain the performance of thin dye-sensitized solar cells （DSSC）. Near-stoichiometric flower-like Cu2ZnSnS4 （CZTS） microspheres with a high specific surface area was fabri- cated for use as the photocathode in a DSSC. To improve the extraction and transfer of electrons, graphene was added to the CZTS. A DSSC with a 10-gin TiO2 pho- toanode layer exhibited a slightly degraded efficiency with a CZTS-graphene photocathode, relative to a Pt counter electrode （CE）. Nevertheless, when the thickness of the TiO2 photoanode was reduced to 2 lam, the efficiency of a DSSC with a CZTS-graphene photocathode was greater than that of a Pt-DSSC. It is speculated that, unlike the Pt CE, a CZTS-graphene photocathode not only collects electrons from an external circuit and catalyzes the reduction of the triiodide ions in the electrolyte, but also utilizes unabsorbed photons to produce photo-excited electrons and suppresses charge recombination, thus enhancing the performance of the cell. The use of narrowband gap p-type semiconductors as photocathodes offers a new means of fabricating thin dye-sensitized solar cells and effectively improving the cell performance.
基金supported by ITER Research Project of China Matched Program (No.2009GB107004)the Fundamental Research Funds for the Central Universities of China (No.ZYGX2010J056)Natural Natural Science Foundation of China (No.11205027)
文摘This paper deals with the profile measurement of impurity ion temperature and toroidal rotation velocity that can be achieved by using the charge exchange recombination spectrum （CXRS） diagnostics tool built on the HL-2A toknmak. By using CXRS, an accurate impurity ion temperature and toroidal plasma rotation velocity profile can be achieved under the condition of neutrM beam injection （NBI） heating. Considering the edge effect of the line of CVI 529.06 nm （n= 8-7）, which contains three lines （active exciting spectral line （ACX）, passivity exciting spectral line （PCX） and electron exciting spectral line （ICE））, and using three Gaussian fitted curves, we obtain the following experimental results： the core ion temperature of HL-2A device is nearly thousands of eV, and the plasma rotation velocity reaches about 104 m· s^-1. At the end of paper, some explanations are presented for the relationship between the curves and the inner physical mechanism.
基金supported by the Instruments R&D Project of the Chinese Academy of Sciences (title: Active Beam Spectra Diagnostic)partially supported by National Natural Science Foundation of China (Nos. 10725523, 10975155)the U. S. Department of Energy Under Grant No. DE-FG02-03ER54729 to the University of Texas
文摘Charge exchange recombination spectroscopy （CXRS） based on a diagnostic neutral beam （DNB） installed in the HT-7 tokamak is introduced. DNB can provide a 6 A extracted current at 50 kV for 0.1 s in hydrogen. It can penetrate into the core plasma in HT-7. The CXRS system is designed to observe charge exchange （CX） transitions in the visible spectrum. CX light from the beam is focused onto 10 optical fibers, which view the plasma from -5 cm to 20 cm. The CXRS system can measure the ion temperature as low as 0.1 keV. With CXRS, the local ion temperature profile in HT-7 was obtained for the first time.
文摘With consideration of the effects of the atomic process and the sight line direction on the charge exchange re-combination spectroscopy （CXRS）, a code used to modify the poloidal CXRS measurement on Tokamak-60 Upgrade （JT-60U） in Japan Atomic Energy Research Institute is developed, offering an effective tool to modify the measurement and analyse experimental results further. The results show that the poloidal velocity of ion is overestimated but the ion temperature is underestimated by the poloidal CXRS measurement, and they also indicate that the effect of observation angle on rotation velocity is a dominant one in a core region （r/a 〈 0.65）, whereas in an edge region where the sight line is nearly normal to the neutral beam, the observation angle effect is very small. The difference between the modified velocity and the neoclassical velocity is not larger than the error in measurement. The difference inside the internal transport barrier （ITB） region is 2-3 times larger than that outside the ITB region, and it increases when the effect of excited components in neutral beam is taken into account. The radial electric field profile is affected greatly by the poloidal rotation term, which possibly indicates the correlation between the poloidal rotation and the transport barrier formation.
基金supported by the National Magnetic Confinement Fusion Science Program of China (No. 2019YFE 03030004)National Natural Science Foundation of China (Nos. 11535013 and 11975232)
文摘Ultrafast charge exchange recombination spectroscopy(UF-CXRS)has been developed on the EAST tokamak(Yingying Li et al 2019 Fusion Eng.Des.146522)to measure fast evolutions of ion temperature and toroidal velocity.Here,we report the preliminary diagnostic measurements after relative sensitivity calibration.The measurement results show a much higher temporal resolution compared with conventional CXRS,benefiting from the usage of a prismcoupled,high-dispersion volume-phase holographic transmission grating and a high quantum efficiency,high-gain detector array.Utilizing the UF-CXRS diagnostic,the fast evolutions of the ion temperature and rotation velocity during a set of high-frequency small-amplitude edgelocalized modes(ELMs)are obtained on the EAST tokamak,which are then compared with the case of large-amplitude ELMs.
基金supported by the National Natural Science Foundation of China (21203185, 21373209)the National Basic Research Program of China (2014CB239400)
文摘Junctions are an important structure that allows charge separation in solar cells and photocatalysts. Here, we studied the charge transfer at an anatase/rutile TiO2 phase junction using time-resolved photoluminescence spectroscopy. Visible （-S00 nm） and near-infrared （NIR, -830 nm） emissions were monitored to give insight into the photoinduced charges of anatase and rutile in the junction, respectively, New fast photoluminescence decay components appeared in the visible emission of futile-phase dominated TiO2 and in the NIR emission of many mixed phase TiO2samples. The fast decays confirmed that the charge separation occurred at the phase junction. The visible emission intensity from the mixed phase TiO2 increased, revealing that charge transfer from rutile to anatase was the main pathway. The charge separation slowed the microsecond time scale photolumines- cence decay rate for charge carriers in both anatase and rutile. However, the millisecond decay of the charge carriers in anatase TiO2 was accelerated, while there was almost no change in the charge carrier dynamics of rutile TiO2. Thus, charge separation at the anatase/rutile phase junction caused an increase in the charge carrier concentration on a microsecond time scale, because of slower electron-hole recombination. The enhanced photocatalytic activity previously observed at ana- tase/rutile phase junctions is likely caused by the improved charge carrier dynamics we report here. These findings may contribute to the development of improved photocatalytic materials.
基金funding from the European Union H2020 programme under Excellence research,ERC grant MOLEMAT(726360)PARASOL(RTI2018-102292-B-I00)from Spanish ministry of Science and Innovation。
文摘Mixed cation and anion based perovskites solar cells exhibited enhanced stability under outdoor conditions,however,it yielded limited power conversion efficiency when TiO_(2) and Spiro-OMeTAD were employed as electron and hole transport layer(ETL/HTL)respectively.The inevitable interfacial recombination of charge carriers at ETL/perovskite and perovskite/HTL interface diminished the efficiency in planar(n-i-p)perovskite solar cells.By employing computational approach for uni-dimensional device simulator,the effect of band offset on charge recombination at both interfaces was investigated.We noted that it acquired cliff structure when the conduction band minimum of the ETL was lower than that of the perovskite,and thus maximized interfacial recombination.However,if the conduction band minimum of ETL is higher than perovskite,a spike structure is formed,which improve the performance of solar cell.An optimum value of conduction band offset allows to reach performance of 25.21%,with an open circuit voltage(VOC)of 1231 mV,a current density JSC of 24.57 mA/cm^(2) and a fill factor of 83.28%.Additionally,we found that beyond the optimum offset value,large spike structure could decrease the performance.With an optimized energy level of Spiro-OMeTAD and the thickness of mixed-perovskite layer performance of 26.56% can be attained.Our results demonstrate a detailed understanding about the energy level tuning between the charge selective layers and perovskite and how the improvement in PV performance can be achieved by adjusting the energy level offset.
基金financially supported by the National Natural Science Foundation of China NSFC (No. 51702038)the Sichuan Science & Technology Program (No. 2020YFG0061)the Recruitment Program for Young Professionals。
文摘Suppressing the nonradiative recombination in the bulk and surface of perovskite film is highly desired to improve the power conversion efficiency(PCE)and stability of halide perovskite solar cells(PSCs).In this study,a benzotriazole derivative(6-chloro-1-hydroxybenzotriazole,Cl-HOBT)is applied to improve the crystallinity and reduce the trap density of methylammonium lead iodide(MAPbI3)perovskite film.Meanwhile,incorporation of Cl-HOBT elongates the photoluminescence carrier lifetime and chargerecombination lifetime,implying the trap-assisted nonradiative recombination is greatly suppressed.Besides,the improved energy level alignment and enhanced built-in potential are conducive to the charge carrier separation and transfer process with Cl-HOBT.Consequently,a PCE of 20.27%and an open-circuit voltage(Voc)of 1.09 V are achieved for the inverted MAPbI3 PSCs,along with an 85%maintaining of the initial PCE under stored at relative humidity of 20%for 500 h.Furthermore,the existence of Cl-HOBT could inhibit the formation of Pb0 defect under prolonged UV illumination to retard the degradation of perovskite film.It is believed that this study paves a novel path for the realization of highefficiency PSCs with UV-stability.
基金supported by the National Natural Science Foundation of China (Nos. 22176029, 21822601, 51908091, and 52200122)the Natural Science Foundation of Chongqing (No. cstc2019jcyj-msxm X0213)+1 种基金the Science and Technology Research Project of Chongqing Education Commission (No. KJQN202200806)the Start-up Foundation of High-level Talents in Chongqing Technology and Business University (Nos. 2256006 and 1856044)。
文摘Crystal defect is well-known to have a significant effect on the photocatalytic performance of semiconductors. Herein, defect-rich and-poor BaSn(OH)6(BSOH-Sn and BSOH-Ba) photocatalysts were synthesized by exchanging the addition order of Ba and Sn. Results show that the defect-poor BSOH-Ba exhibited more efficient toluene degradation under ultraviolet(UV) light, which could attribute to the great suppression of photogenerated electron-hole(e--h+) pairs recombination by tuning the defect concentration. The low defect concentration in BSOH-Ba finally promotes the charge separation efficiency, the generation of reactive oxygen species(ROS), and the photocatalytic toluene degradation reactions. This work not only provides an effective way to inhibit the recombination of photogenerated carriers and improve the photocatalytic performance, but also promotes the understanding of defective perovskite-type hydroxide for more photoreactions.
文摘Influence of recombination centers’ changes on the form of phase portraits has been studied. It has been shown that the shape of the phase portraits depends on the concentration of semiconductor materials’ recombination centers.
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Rare earth element-enhanced TiO2 achieves high-efficiency photocatalytic overall water splitting Photocatalytic water splitting is a clean energy technology that uses sunlight to split water into oxygen and hydrogen in order to produce green hydrogen,a clean fuel,without relying on fossil fuels.The process is driven by a photocatalyst.While titanium dioxide(TiO2)has long been studied as a promising semiconductor for photocatalytic water splitting,its efficiency has been hindered by rapid charge recombination and insufficient charge separation.
基金financially supported by the Fundamental Research Funds for the Central Universities(No.DUT20RC(3)076)Natural Science Foundation of Liaoning Province(No.2020-MS293)。
文摘This study investigates the intersystem crossing(ISC)mechanism in donor-acceptor(D-A)type distyryl-BODIPY photosensitizers,including previously reported M1(benzene donor),M2,M3(phenothiazine donors),and newly predicted M4(triphenylamine donor),M5-M7(nitrogen-containing aliphatic rings with thiophene donors).Using computational chemistry,we analyzed their geometric configurations,spectral properties,spin-orbit coupling,and electron-hole orbitals.We found that S_(2) is a charge transfer singlet state(^(1)CT),T2is a locally excited triplet state(^(3)LE),and the S_(2)→T_(2)transition is the main ISC pathway in M2-M7,following the ^(1)CT→^(3)LE mechanism.M5-M7 show near-vertical dihedral angles between donor and acceptor in the S_(2) state relative to M2-M4,facilitating charge transfer.The strain energies in the nitrogen-containing rings of M5-M7 affect oxidation potentials and ISC.M5,with the highest strain energy,shows the lowest oxidation potential,smaller△_(ES2-T2),highest SOC,and fastest kisc,making it the most efficient predicted singlet oxygen producer.This research clarifies the structure-performance relationships of near-infrared D-A type distyryl-BODIPY photosensitizers and provides a theoretical foundation for developing heavy-atom-free photosensitizers with tuned fluorescence quantum yield and singlet oxygen quantum yield.
基金the National Natural Science Foundation of China(22209144)the Project of the Natural Science Foundation of Yunnan+4 种基金the Yunnan Revitalization Talent Support Program(202201AU070030 and 202201AT070114)the support from the National Natural Science Foundation of China(22065038)the High-Level Talents Introduction in Yunnan Province(C619300A010)the Fund for Excellent Young Scholars of Yunnan(202001AW070008)financial support from the National Research Foundation of Korea(NRF)grant funded by the Korea government(MSIT)under grant number RS-2024-00444389。
文摘2,2',7,7'-Tetrakis(N,N-di(4-methoxyphenyl)amino)-9,9'-spirobifluorene(Spiro)is an essential hole-transport material used in perovskite solar cells(PSCs).However,the redox reaction of Spiro and its impact at the interface with the metal electrode are not yet fully understood.In this study,we introduced a crystalline additive(CA)to regulate the redox process of Spiro and its interface with an Ag electrode.Our findings indicate that CA functions as a molecular scaffold,improving the crystallinity and stability of radicals in Spiro throughout the entire redox reaction.This enhancement increases the hole mobility of Spiro and strengthens the internal electric field,thereby improving hole extraction and transport efficiency at both interfaces.Moreover,the optimized redox reaction of Spiro reduces energy loss at the Ag electrode,significantly boosting the power conversion efficiency to 25.21%.Furthermore,CA mitigates the aggregation of lithium salt and enhances the stability of the device.Our findings contribute to a deeper understanding of hole-transport mechanisms of Spiro and emphasize the importance of reducing energy loss at the Spiro/Ag electrode interface in PSCs.
文摘Semiconductor-cocatalyst interfacial electron transfer has widely been considered as a fast step occurring on picosecond-microsecond timescale in photocatalytic reaction.However,the formed potential barriers severely slow this interfacial electronic process by thermionic emission.Although trap-assisted charge recombination can transfer electrons from semiconductor to cocatalyst and can even be evident under weak illumination,the parallel connection with thermionic emission makes the photocatalytic photon utilization encounter a minimum along the variation of light intensity.By this cognition,the light-intensity-dependent photocatalytic behaviors can be predicted by simulating the photoinduced semiconductor-cocatalyst interfacial electron transfer that mainly determines the reaction rate.We then propose a(photo)electrochemical method to evaluate the time constants for occurring this interfacial electronic process in actual photocatalytic reaction without relying on extremely high photon flux that is required to generate discernible optical signal in common instrumental methods based on ultrafast pulse laser.The evaluated decisecond-second timescale can accurately guide us to develop certain strategies to facilitate this rate-determining step to improve photon utilization.
基金This work was supported by the National Natu- ral Science Foundation of China （No.21072152 and No.21101115）.
文摘Developing photosensitizers suitable for the cobalt electrolyte and understanding the structure-property relationship of organic dyes is warranted for the dye-sensitized solar cells （DSSCs）. The DSSCs incorporating tris（1,10-phenanthroline）eobalt（Ⅱ/Ⅲ）-based redox elec- trolyte and four synthesized organic dyes as photosensitizers are described. The photovoltaic performance of these dyes-sensitized solar cells employing the cobalt redox shuttle and the influences of the w-conjugated spacers of organic dyes upon the photovoltage and photocur- rent of mesoscopic titania solar cells are investigated. It is found that organic dyes with thiophene derivates as linkers are suitable for DSSCs employing cobalt electrolytes. DSSCs sensitized with the as-synthesized dyes in combination with the cobalt redox shuttle yield an overall power conversion efficiency of 6.1% under 100 mW/cm2 AM1.5 G illumination.
基金Qingdao Postdoctoral Funding Program,Grant/Award Number:QDBSH20220201002National Key Research and Development Program of China,Grant/Award Number:2021YFE0111000+1 种基金Project of Shandong Province Higher Educational Young Innovative Team,Grant/Award Number:2022KJ218National Natural Science Foundation of China,Grant/Award Numbers:62104136,22179051,22109053。
文摘Suppressing nonradiative recombination and releasing residual strain areprerequisites to improving the efficiency and stability of perovskite solar cells(PSCs).Here,long-chain polyacrylic acid(PAA)is used to reinforce SnO_(2)film and passivate SnO_(2)defects,forming a structure similar to“reinforcedconcrete”with high tensile strength and fewer microcracks.Simultaneously,PAA is also introduced to the SnO_(2)/perovskite interface as a“buffer spring”torelease residual strain,which also acts as a“dual-side passivation interlayer”to passivate the oxygen vacancies of SnO_(2)and Pb dangling bonds in halideperovskites.As a result,the best inorganic CsPbBr_(3)PSC achieves a championpower conversion efficiency of 10.83%with an ultrahigh open-circuit voltageof 1.674 V.The unencapsulated PSC shows excellent stability under 80%relative humidity and 80℃over 120 days.
基金the National Natural Science Foundation of China(61774139,U1802257)Director Foundation from Qingdao National Laboratory for Marine Science and Technology(QNLM201702)+2 种基金Postdoctoral Research Foundation of China(2019M650231,2019M663379)the Natural Science Foundation of Guangdong Province(2019B151502061)the Fundamental Research Funds for the Central Universities(11618409,11619311)。
文摘Tin dioxide(SnO2) is generally regarded as a promising electron-transporting layer(ETL) for state-of-theart perovskite solar cells(PSCs), however, the ubiquitous oxygen-vacancy-related defects at SnO2 surface and the large energy difference between conduction band of SnO2 and perovskite layer undoubtedly cause severe charge carrier recombination, resulting in sluggish charge extraction efficiency and non-negligible open-circuit voltage(Voc) loss. Herein, a chlorine-containing TiOxCl4-2x accessory layer is fabricated by immersing SnO2 layer into the TiCl4 aqueous solution to passivate the surface oxygen-vacancy-related defects of SnO2 layer and to set an intermediate energy level at ETL/perovskite interface in all-inorganic cesium lead tri-bromine(CsPbBr3) PSCs. Furthermore, the TiOxCl4-2x layer also improves the infiltration of SnO2 layer surface toward perovskite precursor for high-quality perovskite film. Finally, the hole-free, allinorganic CsPbBr3PSC with a structure of FTO/SnO2/TiOxCl4-2x/Cs0.91Rb0.09PbBr3/carbon achieves a champion efficiency of 10.44% with a Vocas high as 1.629 V in comparison to 8.31% for control device. Moreover, the optimized solar cell presents good stability in 80% humidity in air.
文摘In the present investigation,a new composite nanostructured photoanodes were prepared using TiO_2 nanotubes（TNTs） with TiO_2 nanoparticles（TNPs）.TNPs were synthesized by sol-gel method,and TNTs were prepared through alkali hydrothermal method.Dye-sensitized solar cells（DSSCs） were fabricated with different photoanodes comprising of various ratios of TNTs ＋ TNPs,synthetic indigo dye as photosensitizer,PMII（l-propyl-3-methylimidazolium iodide） as ionic liquid electrolyte and cobalt sulfide as counter electrode.The structures and morphologies of TNPs and TNTs were analyzed through X-ray diffractometer,transmission electron microscope and scanning electron microscopes.The results of the investigation showed that the DSSC-4 made with composite photoanode structure（TNTs/TNPs）（90% of TNPs ＋ 10% of TNTs） had improved photocurrent efficiency（2.11%） than pure TNPs（1.00%） and TNT film（0.78%）.Electrochemical impedance spectra revealed that the composite TNTs/TNPs film-based DSSCs possessed the lowest charge-transfer resistances and longest electron lifetime.Hence,it could be concluded that the composite TNTs/TNPs photoanode facilitates the charge transport rate and enhances the efficiencies of DSSCs.
