Compared to organic-inorganic hybrid perovskites,the cesium-based allinorganic lead halide perovskite(CsPbI_(3))is a promising light absorber for perovskite solar cells owing to its higher resistance to thermal stress...Compared to organic-inorganic hybrid perovskites,the cesium-based allinorganic lead halide perovskite(CsPbI_(3))is a promising light absorber for perovskite solar cells owing to its higher resistance to thermal stress.Nonetheless,additional research is required to reduce the nonradiative recombination to realize the full potential of CsPbI_(3).Here,the diffusion of Cs ions participating in ion exchange is proposed to be an important factor responsible for the bulk defects inγ-CsPbI_(3)perovskite.Calculations based on first-principles density functional theory reveal that the[PbI_(6)]^(4-)octahedral tilt modifies the perovskite crystallographic properties inγ-CsPbI_(3),leading to alterations in its bandgap and crystal strain.In addition,by substituting amorphous barium titanium oxide(a-BaTiO_(3))for TiO_(2)as the electron transport layer,interfacial defects caused by imperfect energy levels between the electron transport layer and perovskite are reduced.High-resolution transmission electron microscopy and electron energy loss spectroscopy demonstrate that a-BaTiO_(3)forms entirely as a single phase,as opposed to Ba-doped TiO_(2)hybrid nanoclusters or separate domains of TiO_(2)and BaTiO_(3)phases.Accordingly,inorganic perovskite solar cells based on the a-BaTiO_(3)electron transport layer achieved a power conversion efficiency of 19.96%.展开更多
To enhance the piezoelectric performance of piezoelectric polymer thin films in general,hybrid polyvinylidene difluoride(PVDF)and nanosized barium titanate(BaTiO_(3))piezoelectric films were prepared and their piezoel...To enhance the piezoelectric performance of piezoelectric polymer thin films in general,hybrid polyvinylidene difluoride(PVDF)and nanosized barium titanate(BaTiO_(3))piezoelectric films were prepared and their piezoelectric performance examined.The hybrid nanofibers were fabricated via electrospinning at an external voltage of 15 kV.The nonwoven fabrics were collected using a roller collection device,and their morphological structures were analyzed via scanning electron microscopy.The crystal structures of these piezoelectric films were characterized via micro-Raman spectroscopy.β-phase of the composite nanofiber membrane almost increased to twice owing to the addition of BaTiO_(3)nanoparticles.Compared with pure,electrospun PVDF piezoelectric film,the piezoelectric characteristics of the hybrid piezoelectric films were considerably enhanced because of the additional BaTiO_(3)nanoparticles.The maximum instantaneous open-circuit voltage of the hybrid PVDF-BaTiO_(3)nanofibers film can be high up to 80 V.The high-performance hybrid piezoelectric films exhibited notable prospects for applications in wearable electronic textiles.展开更多
基金supported by the Korea Institute of Energy Technology Evaluation and Planning(KETEP)granted financial resource from the Ministry of Trade,Industry&Energy,Republic of Korea(20213091010020)the Korea Institute of Planning and Evaluation for Technology in Food,Agriculture and Forestry(IPET)and Korea Smart Farm R&D Foundation(KosFarm)through Smart Farm Innovation Technology Development Programfunded by Ministry of Agriculture,Food and Rural Affairs(MAFRA),Ministry of Science and ICT(MSIT),Rural Development Administration(RDA)(421036-03)
文摘Compared to organic-inorganic hybrid perovskites,the cesium-based allinorganic lead halide perovskite(CsPbI_(3))is a promising light absorber for perovskite solar cells owing to its higher resistance to thermal stress.Nonetheless,additional research is required to reduce the nonradiative recombination to realize the full potential of CsPbI_(3).Here,the diffusion of Cs ions participating in ion exchange is proposed to be an important factor responsible for the bulk defects inγ-CsPbI_(3)perovskite.Calculations based on first-principles density functional theory reveal that the[PbI_(6)]^(4-)octahedral tilt modifies the perovskite crystallographic properties inγ-CsPbI_(3),leading to alterations in its bandgap and crystal strain.In addition,by substituting amorphous barium titanium oxide(a-BaTiO_(3))for TiO_(2)as the electron transport layer,interfacial defects caused by imperfect energy levels between the electron transport layer and perovskite are reduced.High-resolution transmission electron microscopy and electron energy loss spectroscopy demonstrate that a-BaTiO_(3)forms entirely as a single phase,as opposed to Ba-doped TiO_(2)hybrid nanoclusters or separate domains of TiO_(2)and BaTiO_(3)phases.Accordingly,inorganic perovskite solar cells based on the a-BaTiO_(3)electron transport layer achieved a power conversion efficiency of 19.96%.
基金The National Natural Science Foundation of China(No.52375563)the Science and Technology on Avionics Integration Laboratory(No.201913069001,20200055069001).
文摘To enhance the piezoelectric performance of piezoelectric polymer thin films in general,hybrid polyvinylidene difluoride(PVDF)and nanosized barium titanate(BaTiO_(3))piezoelectric films were prepared and their piezoelectric performance examined.The hybrid nanofibers were fabricated via electrospinning at an external voltage of 15 kV.The nonwoven fabrics were collected using a roller collection device,and their morphological structures were analyzed via scanning electron microscopy.The crystal structures of these piezoelectric films were characterized via micro-Raman spectroscopy.β-phase of the composite nanofiber membrane almost increased to twice owing to the addition of BaTiO_(3)nanoparticles.Compared with pure,electrospun PVDF piezoelectric film,the piezoelectric characteristics of the hybrid piezoelectric films were considerably enhanced because of the additional BaTiO_(3)nanoparticles.The maximum instantaneous open-circuit voltage of the hybrid PVDF-BaTiO_(3)nanofibers film can be high up to 80 V.The high-performance hybrid piezoelectric films exhibited notable prospects for applications in wearable electronic textiles.