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dc.contributor.authorXiao, Xun
dc.contributor.authorZhou, Jian
dc.contributor.authorSong, Kepeng
dc.contributor.authorZhao, Jingjing
dc.contributor.authorZhou, Yu
dc.contributor.authorRudd, Peter
dc.contributor.authorHan, Yu
dc.contributor.authorLi, Ju
dc.contributor.authorHuang, Jinsong
dc.date.accessioned2020-12-02T07:45:33Z
dc.date.available2020-12-02T07:45:33Z
dc.date.issued2020-11-30
dc.identifier.citationXiao, X., Zhou, J., Song, K., Zhao, J., Zhou, Y., Rudd, P., … Huang, J. (2020). Layer Number Dependent Ferroelasticity in 2D Ruddlesden-Popper Organic-inorganic Hybrid Perovskites. doi:10.21203/rs.3.rs-109794/v1
dc.identifier.doi10.21203/rs.3.rs-109794/v1
dc.identifier.urihttp://hdl.handle.net/10754/666220.1
dc.description.abstractAbstract Ferroelasticity represents material domains possessing spontaneous strain that can be switched by external stress. Three-dimensional (3D) perovskites like methylammonium lead iodide (MAPI), which have demonstrated efficient solar cells and photodetectors, are determined to be ferroelastic. Apart from 3D perovskites, Ruddlesden-popper layered perovskites have been applied in optoelectronic devices with outstanding performance. However, the understanding of lattice strain as well as ferroelasticity in 2D layered perovskites is still lacking. Here,using the in-situ observation of switching domains in layered perovskite single crystals under external strain, we discover the existence of ferroelasticity in layered perovskites with layer number more than one, while the 2D perovskites with single octahedra layer do not show ferroelasticity. Density functional theory calculation shows that ferroelasticity in 2D perovskites originates from the distortion of inorganic octahedra resulting from the rotation of aspherical methylammonium cations. Additionally, the absence of methylammonium cations in single layer perovskite is consistent with the lack of ferroelasticity. These ferroelastic domains do not induce non-radiative recombination or reduce the photoluminescence quantum yield appreciably, indicating the glissile ferroelastic twin boundaries are benign defects. Our findings provide scientific insights in understanding strain-dependent material properties in 2D perovskites and lead to new potential flexible electronics controlled by strain engineering.
dc.description.sponsorshipThe experimental work at UNC is nancially supported by Center for Hybrid Organic Inorganic Semiconductors for Energy (CHOISE), an Energy Frontier Research Center funded by the Oce of Basic Energy Sciences, Oce of Science within the US Department of Energy. Huang and Li also thank the nancial support from the Department of the Defense, Defense Threat Reduction Agency under award HDTRA1-20-2-0002. The content of the information does not necessarily reect the position or the policy of the federal government, and no ocial endorsement should be inferred.
dc.publisherResearch Square
dc.relation.urlhttps://www.researchsquare.com/article/rs-109794/v1
dc.rightsArchived with thanks to Research Square
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleLayer Number Dependent Ferroelasticity in 2D Ruddlesden-Popper Organic-inorganic Hybrid Perovskites
dc.typePreprint
dc.contributor.departmentAdvanced Membranes and Porous Materials Research Center
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.contributor.departmentChemical Science Program
dc.eprint.versionPre-print
dc.contributor.institutionUniversity of North Carolina at Chapel Hill
dc.contributor.institutionXi'an Jiaotong University
dc.contributor.institutionUniversity of North Carolina, Chapel Hill
dc.contributor.institutionMassachusetts Institute of Technology
kaust.personSong, Kepeng
kaust.personHan, Yu
refterms.dateFOA2020-12-02T07:46:53Z


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