Epitaxial YBCO films were deposited on (100) LaAlO3 single-crystal substrates by metalorganic deposition of metal trifluoroacetate precursors with different concentrations. All the YBCO films have Tc around 91 K and...Epitaxial YBCO films were deposited on (100) LaAlO3 single-crystal substrates by metalorganic deposition of metal trifluoroacetate precursors with different concentrations. All the YBCO films have Tc around 91 K and Jc excess 2 MA/cm^2 at 77 K in zero field. XRD θ-2θscans show all the films have c-axis normal orientation. The FWHM (full width at half-maximum intensity) values of X-ray ω-scans of (005) reflection are 0.379°, 0.283°, and 0.543° for the YBCO thin films deposited with precursor solution concentrations of 1.52, 1.0, and 0.75 mol/L, respectively. With the concentration of the precursors decreasing, the thickness of the films decreases linearly. SEM micrographs show that porosities in the films become bigger with the precursor solution concentration decreasing. The big porosities in the film with the lowest concentration precursor deteriorate the superconducting property and make it have a wider superconducting transition and a lower Jc.展开更多
Formamidinium lead triiodide(FAPbI_(3))is a research hotspot in perovskite photovoltaics due to its broad light absorption and proper thermal stability.However,quite a few researches focused on the stability of the FA...Formamidinium lead triiodide(FAPbI_(3))is a research hotspot in perovskite photovoltaics due to its broad light absorption and proper thermal stability.However,quite a few researches focused on the stability of the FAPbI_(3) perovskite precursor solutions.Besides,the most efficient FAPbI_(3) layers are prepared by the spin-coating method,which is limited to the size of the device.Herein,the stability of FAPbI_(3) perovskite solution with methylammonium chloride(MACl)or cesium chloride(CsCl)additive is studied for preparing perovskite film through an upscalable blade-coating method.Each additive works well for achieving a high-quality FAPbI_(3) film,resulting in efficient carbon electrode perovskite solar cells(pero-SCs)in the ambient condition.However,the perovskite solution with MACl additive shows poor aging stability that noα-FAPbI_(3) phase is observed when the solution is aged over one week.While the perovskite solution with CsCl additive shows promising aging stability that it still forms high-quality pureα-FAPbI_(3) perovskite film even the solution is aged over one month.During the solution aging process,the MACl could be decomposed into methylamine which will form some unfavored intermediated phase inducingδ-phase FAPbI_(3).Whereas,replacing MACl with CsCl could effectively solve this issue.Our founding shows that there is a great need to develop a non-MACl FAPbI_(3) perovskite precursor solution for cost-effective preparation of pero-SCs.展开更多
Pb0.97La0.02Zr0.95Ti0.05O3(PLZT)antiferroelectric thick films derived from different precursor solution concentrations are prepared on platinized silicon substrates by sol-gel processing.The films present polycrystall...Pb0.97La0.02Zr0.95Ti0.05O3(PLZT)antiferroelectric thick films derived from different precursor solution concentrations are prepared on platinized silicon substrates by sol-gel processing.The films present polycrystalline perovskite structure with a(100)preferred orientation by X-ray diffraction(XRD)analysis.The antiferroelectricity of the films is confirmed by the double hysteresis behaviors of polarization and double-bufferfly response of dielectric constant under the applied electrical field.Antiferroelectric properties and dielectric constant are improved while the polarization characteristic values are reduced with the increase of precursor solution concentration.The films at higher precursor solution concentration exhibit excellent dielectric properties.展开更多
Recently,perovskite solar cells(PSCs) have flourished,and their power conversion efficiency(PCE) has increased from the initial 3.8% to 25.2% in 2019,which is an unprecedented advance.However,usually high-efficiency a...Recently,perovskite solar cells(PSCs) have flourished,and their power conversion efficiency(PCE) has increased from the initial 3.8% to 25.2% in 2019,which is an unprecedented advance.However,usually high-efficiency and stable PSCs are small-area devices prepared by spin coating.This method is not suitable for the preparation of large-area devices in commercialization.Therefore,there is an urgent need to develop new materials and methods for the scalable fabrication of PSCs.In this review,we first describe the common small-area PSCs preparation methods,understand the nucleation and crystal growth kinetics of perovskite,and analyze the reasons that hinder the development of small-area devices to large-area devices.Next,in order to meet the challenges of PSC’s scalable fabrication,we summarize and analyze four strategies:scaling up precursor solutions,scalable deposition methods for large-area films,scaling up charge-transport layers and back electrodes,developing solar modules.Finally,challenges and prospects are proposed to help researchers prepare high-efficiency large-area PSCs.展开更多
Perovskite solar cells(PSCs)are promising next-generation photovoltaics due to their unique optoelectronic properties and rapid rise in power conversion efficiency.However,the instability of perovskite materials and d...Perovskite solar cells(PSCs)are promising next-generation photovoltaics due to their unique optoelectronic properties and rapid rise in power conversion efficiency.However,the instability of perovskite materials and devices is a serious obstacle hindering technology commercialization.The quality of perovskite films,which is an important prerequisite for long-term stable PSCs,is determined by the quality of the precursor solution and the post-deposition treatment performed after perovskite formation.Herein,we review the origin of instability of solution-processed PSCs from the perspectives of the precursor solutions and the perovskite films.In addition,we summarize the recent strategies for improving the stability of the perovskite films.Finally,we pinpoint possible approaches to further advance their long-term stability.展开更多
The basis of the hydrophobicity of lanthanide rare earth oxides(REOs)has been the subject of considerable debate.To explore this question,the wetting behaviors and surface compositions of hierarchicallystructured Yb_(...The basis of the hydrophobicity of lanthanide rare earth oxides(REOs)has been the subject of considerable debate.To explore this question,the wetting behaviors and surface compositions of hierarchicallystructured Yb_(2)o_(3)(one of the REOs)coatings and non-REO Al_(2)o_(3)coatings deposited via solution precursor plasma spray process were investigated in this work.The Yb_(2)o_(3)coatings were subjected to a number of post-deposition treatments including vacuum(1-15 Pa)treatment,Ar-plasma treatment,heat treatment(400℃),long-time air exposure and ultra-high vacuum(1×10^(-7)Pa)treatment.Subsequent characterization showed that different post-deposition treatments resulted in different wetting behavior for the Yb_(2)o_(3)coatings which correlated with the content of hydrocarbon on the surface.Yb_(2)o_(3)coatings exhibited reversible transitions between superhydrophobicity after vacuum treatment and superhydrophilicity after Ar-plasma or heat treatment,linked to hydrocarbon adsorption onto and desorption from the surface.Yb_(2)o_(3)coatings after long-time air exposure and ultra-high vacuum treatment both remained hydrophilic and showed a smaller hydrocarbon content than coatings after vacuum treatment.Al_(2)o_(3)coatings with hierarchical surface structures similar to the Yb_(2)o_(3)coatings showed an increase in WCA to only-170 after the same vacuum treatment,indicating the REO has a much higher affinity for hydrocarbon adsorption than Al_(2)o_(3),and that the content of hydrocarbon adsorbed on the surface of the REO determined the wetting behavior.展开更多
Cu-rich cell boundary phase is difficult to precipitate evenly,resulting in a generally poor demagnetization curve squareness for Fe-rich Sm_(2)Co_(17)-type magnet,which is a key factor limiting the further improvemen...Cu-rich cell boundary phase is difficult to precipitate evenly,resulting in a generally poor demagnetization curve squareness for Fe-rich Sm_(2)Co_(17)-type magnet,which is a key factor limiting the further improvement of magnetic energy product.In this study,we report that nanoscale strip-like ordered micro-domains distributed in1:7H disordered matrix phase of the solid solution precursor is a new factor significantly affecting the precipitation and distribution of the cell boundary phase.Long strip-like and continuous micro-twin structure with twin boundaries neatly perpendicular to the C-axis is observed after sintering treatment.After solution treatment,sequential and long strip-like micro-twins gradually transform into disordered state along the basal plane,forming narrow disordered 1:7H(TbCu_(7)-type structure)phase between the separated strip-like ordered micro-domains.This disordering transformation takes place via broken down of the long strip-like ordered micro-domains,which is accomplished by narrowing along the width direction followed by reduction of the length.Furthermore,a new model revealing the effect of the ordered micro-domains on the formation of the cell boundary phase is proposed.Antiphase boundaries enriched in Cu have already existed in the precursor with long strip-like ordered micro-domains.Therefore,the Cu-rich cell boundary phase acting as strong pinning centers cannot be precipitated homogeneously and distributed continuously after aging,resulting in a poor demagnetization curve squareness of Sm_(2)Co_(17)-type magnet.Our results indicate that significant broken down of the nanoscale ordered micro-domains in solution precursor is the key factor improving the distribution of cell boundary phase in Sm_(2)Co_(17)-type magnets.展开更多
Selective-controlled structure and shape of CeVO4 nanocrystals were successfully synthesized via a hydrothermal method from Na3VO4·12H2O and Ce(NO3)3·6H2O.The resulting products were characterized by X-ray...Selective-controlled structure and shape of CeVO4 nanocrystals were successfully synthesized via a hydrothermal method from Na3VO4·12H2O and Ce(NO3)3·6H2O.The resulting products were characterized by X-ray powder diffraction (XRD),field emission scanning electron microscopy (FESEM) and energy dispersive spectroscopy (EDS).The influence of hydrothermal temperature,precursor solution concentration on the crystal and morphology of products were further studied.The results showed that the as-synthesized products exhibited pure single-crystal CeVO4 nanoparticles with tetragonal structure.The hydrothermal temperature and precursor solution concentration had important effects on the formation of CeVO4 nanoparticles.Furthermore,the growth mechanism of CeVO4 nanoparticles was explained with Ostwald ripening mechanism.展开更多
We systematically investigated the development of film morphology and crystallinity of methyl-ammonium bismuth (Ⅲ) iodide (MA3Bi2I9) through one- step spin-coating on TiO2-deposited indium tin oxide (ITO)/glass...We systematically investigated the development of film morphology and crystallinity of methyl-ammonium bismuth (Ⅲ) iodide (MA3Bi2I9) through one- step spin-coating on TiO2-deposited indium tin oxide (ITO)/glass. The precursor solution concentration and substrate structure have been demonstrated to be critically important in the active-layer evolution of the MA3Bi2I9-based solar cell. This work successfully improved the cell efficiency to 0.42% (average: 0.38%) with the mesoscopic architecture of ITO/compact-TiOdmesoscopic-TiO2 (meso-TiO2)/ MA3Bi2I9/2,2',7,7'-tetrakis(N,N-di-4-methoxyphenylamino)-9,9'spiro-bifluorene (spiro-MeOTAD)/MoO3/Ag under a precursor concentration of 0.45 M, which provided the probability of further improving the efficiency of the BiB+-based lead-free organic-inorganic hybrid solar cells.展开更多
文摘Epitaxial YBCO films were deposited on (100) LaAlO3 single-crystal substrates by metalorganic deposition of metal trifluoroacetate precursors with different concentrations. All the YBCO films have Tc around 91 K and Jc excess 2 MA/cm^2 at 77 K in zero field. XRD θ-2θscans show all the films have c-axis normal orientation. The FWHM (full width at half-maximum intensity) values of X-ray ω-scans of (005) reflection are 0.379°, 0.283°, and 0.543° for the YBCO thin films deposited with precursor solution concentrations of 1.52, 1.0, and 0.75 mol/L, respectively. With the concentration of the precursors decreasing, the thickness of the films decreases linearly. SEM micrographs show that porosities in the films become bigger with the precursor solution concentration decreasing. The big porosities in the film with the lowest concentration precursor deteriorate the superconducting property and make it have a wider superconducting transition and a lower Jc.
基金Project supported by the Key Research and Development Program of China(Grant No.2020YFB1506400)the National Natural Science Foundation of China(Grant Nos.51922074,51673138,51820105003,and 22075194)+1 种基金the Tang Scholar,the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)Collaborative Innovation Center of Suzhou Nano Science and Technology.
文摘Formamidinium lead triiodide(FAPbI_(3))is a research hotspot in perovskite photovoltaics due to its broad light absorption and proper thermal stability.However,quite a few researches focused on the stability of the FAPbI_(3) perovskite precursor solutions.Besides,the most efficient FAPbI_(3) layers are prepared by the spin-coating method,which is limited to the size of the device.Herein,the stability of FAPbI_(3) perovskite solution with methylammonium chloride(MACl)or cesium chloride(CsCl)additive is studied for preparing perovskite film through an upscalable blade-coating method.Each additive works well for achieving a high-quality FAPbI_(3) film,resulting in efficient carbon electrode perovskite solar cells(pero-SCs)in the ambient condition.However,the perovskite solution with MACl additive shows poor aging stability that noα-FAPbI_(3) phase is observed when the solution is aged over one week.While the perovskite solution with CsCl additive shows promising aging stability that it still forms high-quality pureα-FAPbI_(3) perovskite film even the solution is aged over one month.During the solution aging process,the MACl could be decomposed into methylamine which will form some unfavored intermediated phase inducingδ-phase FAPbI_(3).Whereas,replacing MACl with CsCl could effectively solve this issue.Our founding shows that there is a great need to develop a non-MACl FAPbI_(3) perovskite precursor solution for cost-effective preparation of pero-SCs.
基金National Natural Science Foundation of China(No.60806039,No.51175483)China Postdoctoral Science Foundation Projects(No.20090461275,No.201003658)+1 种基金Shanxi Provincial Natural Science Foundation of China(No.20100210023-6)Shanxi Provincial Young Leaders on Science
文摘Pb0.97La0.02Zr0.95Ti0.05O3(PLZT)antiferroelectric thick films derived from different precursor solution concentrations are prepared on platinized silicon substrates by sol-gel processing.The films present polycrystalline perovskite structure with a(100)preferred orientation by X-ray diffraction(XRD)analysis.The antiferroelectricity of the films is confirmed by the double hysteresis behaviors of polarization and double-bufferfly response of dielectric constant under the applied electrical field.Antiferroelectric properties and dielectric constant are improved while the polarization characteristic values are reduced with the increase of precursor solution concentration.The films at higher precursor solution concentration exhibit excellent dielectric properties.
基金funded by the National Natural Science Foundation of China(51902148,61704099,51801088 and 51802024)the Fundamental Research Funds for the Central Universities(lzujbky2020-61,lzujbky-2019-88 and lzujbky-2020-kb06)the Special Funding for Open and Shared Large-Scale Instruments and Equipments of Lanzhou University(LZU-GXJJ-2019C023 and LZU-GXJJ-2019C019)。
文摘Recently,perovskite solar cells(PSCs) have flourished,and their power conversion efficiency(PCE) has increased from the initial 3.8% to 25.2% in 2019,which is an unprecedented advance.However,usually high-efficiency and stable PSCs are small-area devices prepared by spin coating.This method is not suitable for the preparation of large-area devices in commercialization.Therefore,there is an urgent need to develop new materials and methods for the scalable fabrication of PSCs.In this review,we first describe the common small-area PSCs preparation methods,understand the nucleation and crystal growth kinetics of perovskite,and analyze the reasons that hinder the development of small-area devices to large-area devices.Next,in order to meet the challenges of PSC’s scalable fabrication,we summarize and analyze four strategies:scaling up precursor solutions,scalable deposition methods for large-area films,scaling up charge-transport layers and back electrodes,developing solar modules.Finally,challenges and prospects are proposed to help researchers prepare high-efficiency large-area PSCs.
基金supported by the National Natural Science Foundation of China(22109166 and 22279083)the Chinese Academy of Sciences.
文摘Perovskite solar cells(PSCs)are promising next-generation photovoltaics due to their unique optoelectronic properties and rapid rise in power conversion efficiency.However,the instability of perovskite materials and devices is a serious obstacle hindering technology commercialization.The quality of perovskite films,which is an important prerequisite for long-term stable PSCs,is determined by the quality of the precursor solution and the post-deposition treatment performed after perovskite formation.Herein,we review the origin of instability of solution-processed PSCs from the perspectives of the precursor solutions and the perovskite films.In addition,we summarize the recent strategies for improving the stability of the perovskite films.Finally,we pinpoint possible approaches to further advance their long-term stability.
基金supported by Natural Science and Engineering Research Council Canada Discovery Grants Program(No.RGPIN-2015-06377(TWC))Natural Science and Engineering Research Council Canada Green Surface Engineering for Advanced Manufacturing(Green-SEAM)Strategic Network。
文摘The basis of the hydrophobicity of lanthanide rare earth oxides(REOs)has been the subject of considerable debate.To explore this question,the wetting behaviors and surface compositions of hierarchicallystructured Yb_(2)o_(3)(one of the REOs)coatings and non-REO Al_(2)o_(3)coatings deposited via solution precursor plasma spray process were investigated in this work.The Yb_(2)o_(3)coatings were subjected to a number of post-deposition treatments including vacuum(1-15 Pa)treatment,Ar-plasma treatment,heat treatment(400℃),long-time air exposure and ultra-high vacuum(1×10^(-7)Pa)treatment.Subsequent characterization showed that different post-deposition treatments resulted in different wetting behavior for the Yb_(2)o_(3)coatings which correlated with the content of hydrocarbon on the surface.Yb_(2)o_(3)coatings exhibited reversible transitions between superhydrophobicity after vacuum treatment and superhydrophilicity after Ar-plasma or heat treatment,linked to hydrocarbon adsorption onto and desorption from the surface.Yb_(2)o_(3)coatings after long-time air exposure and ultra-high vacuum treatment both remained hydrophilic and showed a smaller hydrocarbon content than coatings after vacuum treatment.Al_(2)o_(3)coatings with hierarchical surface structures similar to the Yb_(2)o_(3)coatings showed an increase in WCA to only-170 after the same vacuum treatment,indicating the REO has a much higher affinity for hydrocarbon adsorption than Al_(2)o_(3),and that the content of hydrocarbon adsorbed on the surface of the REO determined the wetting behavior.
基金financially supported by the National Key R&D Program of China(No.2021YFB3503102)Zhejiang Provincial Key R&D Program(No.2021C01191)+2 种基金Science and Technology Innovation 2025 Major Project of Ningbo(No.2020Z037)Ningbo Key R&D Program(No.20222ZDYF020027)Ningbo Natural Science Foundation(No.2021J216)。
文摘Cu-rich cell boundary phase is difficult to precipitate evenly,resulting in a generally poor demagnetization curve squareness for Fe-rich Sm_(2)Co_(17)-type magnet,which is a key factor limiting the further improvement of magnetic energy product.In this study,we report that nanoscale strip-like ordered micro-domains distributed in1:7H disordered matrix phase of the solid solution precursor is a new factor significantly affecting the precipitation and distribution of the cell boundary phase.Long strip-like and continuous micro-twin structure with twin boundaries neatly perpendicular to the C-axis is observed after sintering treatment.After solution treatment,sequential and long strip-like micro-twins gradually transform into disordered state along the basal plane,forming narrow disordered 1:7H(TbCu_(7)-type structure)phase between the separated strip-like ordered micro-domains.This disordering transformation takes place via broken down of the long strip-like ordered micro-domains,which is accomplished by narrowing along the width direction followed by reduction of the length.Furthermore,a new model revealing the effect of the ordered micro-domains on the formation of the cell boundary phase is proposed.Antiphase boundaries enriched in Cu have already existed in the precursor with long strip-like ordered micro-domains.Therefore,the Cu-rich cell boundary phase acting as strong pinning centers cannot be precipitated homogeneously and distributed continuously after aging,resulting in a poor demagnetization curve squareness of Sm_(2)Co_(17)-type magnet.Our results indicate that significant broken down of the nanoscale ordered micro-domains in solution precursor is the key factor improving the distribution of cell boundary phase in Sm_(2)Co_(17)-type magnets.
基金financial support by the Open Project Program of the State Key Laboratory of Solid Lu-brication, Lanzhou Institute of Chemical Physics,Chinese Academy of Sciences (0804)
文摘Selective-controlled structure and shape of CeVO4 nanocrystals were successfully synthesized via a hydrothermal method from Na3VO4·12H2O and Ce(NO3)3·6H2O.The resulting products were characterized by X-ray powder diffraction (XRD),field emission scanning electron microscopy (FESEM) and energy dispersive spectroscopy (EDS).The influence of hydrothermal temperature,precursor solution concentration on the crystal and morphology of products were further studied.The results showed that the as-synthesized products exhibited pure single-crystal CeVO4 nanoparticles with tetragonal structure.The hydrothermal temperature and precursor solution concentration had important effects on the formation of CeVO4 nanoparticles.Furthermore,the growth mechanism of CeVO4 nanoparticles was explained with Ostwald ripening mechanism.
基金This work was supported by the National Basic Research Program of China (No. 2014CB643503), the National Natural Science Foundation of China (Nos. 91233114, 51373151 Zhejiang Province Natural LR15E030001). and 51261130582) and Science Foundation (No.
文摘We systematically investigated the development of film morphology and crystallinity of methyl-ammonium bismuth (Ⅲ) iodide (MA3Bi2I9) through one- step spin-coating on TiO2-deposited indium tin oxide (ITO)/glass. The precursor solution concentration and substrate structure have been demonstrated to be critically important in the active-layer evolution of the MA3Bi2I9-based solar cell. This work successfully improved the cell efficiency to 0.42% (average: 0.38%) with the mesoscopic architecture of ITO/compact-TiOdmesoscopic-TiO2 (meso-TiO2)/ MA3Bi2I9/2,2',7,7'-tetrakis(N,N-di-4-methoxyphenylamino)-9,9'spiro-bifluorene (spiro-MeOTAD)/MoO3/Ag under a precursor concentration of 0.45 M, which provided the probability of further improving the efficiency of the BiB+-based lead-free organic-inorganic hybrid solar cells.