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dc.contributor.authorZhou, Wencai
dc.contributor.authorZheng, Zilong
dc.contributor.authorLu, Yue
dc.contributor.authorSui, Manling
dc.contributor.authorYin, Jun
dc.contributor.authorYan, Hui
dc.date.accessioned2021-06-09T06:46:15Z
dc.date.available2021-06-09T06:46:15Z
dc.date.issued2021
dc.date.submitted2021-02-23
dc.identifier.citationZhou, W., Zheng, Z., Lu, Y., Sui, M., Yin, J., & Yan, H. (2021). Understanding liquefaction in halide perovskites upon methylamine gas exposure. RSC Advances, 11(33), 20423–20428. doi:10.1039/d1ra01458g
dc.identifier.issn2046-2069
dc.identifier.doi10.1039/d1ra01458g
dc.identifier.urihttp://hdl.handle.net/10754/669475
dc.description.abstractMethylamine (CH3NH2, MA) gas-induced fabrication of organometal CH3NH3PbI3 based perovskite thin films are promising photovoltaic materials that transform the energy from absorbed sunlight into electrical power. Unfortunately, the low stability of the perovskites poses a serious hindrance for further development, compared to conventional inorganic materials. The solid-state perovskites are liquefied and recrystallized from CH3NH2. However, the mechanism of this phase transformation is far from clear. Employing first principles calculations and ab initio molecular dynamics simulations, we investigated the formation energy of primary defects in perovskites and the liquefaction process in CH3NH2 vapor. The results indicated that defect-assisted surface dissolution leads to the liquefaction of perovskite thin films in CH3NH2 vapor. Two primary defects were studied: one is the Frenkel pair defect (including both negatively charged interstitial iodide ion (Ii−) and iodide vacancy (VI+) at the PbI2-termination surface, and the other is the Schottky defects (methylammonium vacancy, VMA) at the MAI-termination surface. Moreover, the defect-induced disorder in the microstructure reduces the degeneration of energy levels, which leads to a blue shift and broader absorption band gap, as compared to the clean perovskite surface. The mechanism of how defects impact the surface dissolution could be applied for the further design of high-stability perovskite solar cells.
dc.description.sponsorshipThis work was financially supported by the National Natural Science Foundation of China (No. 62034001, 22033006, 52073005). We also acknowledge for the financial support from Key Laboratory of Advanced Functional Materials, Education Ministry of China, and supercomputer center of Institute of Advanced Energy Materials and Devices in BJUT.
dc.publisherRoyal Society of Chemistry (RSC)
dc.relation.urlhttp://xlink.rsc.org/?DOI=D1RA01458G
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/
dc.titleUnderstanding liquefaction in halide perovskites upon methylamine gas exposure
dc.typeArticle
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.identifier.journalRSC Advances
dc.eprint.versionPublisher's Version/PDF
dc.contributor.institutionFaculty of Materials and Manufacturing
dc.contributor.institutionBeijing University of Technology
dc.contributor.institutionBeijing 100124
dc.contributor.institutionChina
dc.contributor.institutionDivision of Physical Science and Engineering
dc.contributor.institutionKingdom of Saudi Arabia
dc.identifier.volume11
dc.identifier.issue33
dc.identifier.pages20423-20428
kaust.personYin, Jun
kaust.personYin, Jun
dc.date.accepted2021-05-04
refterms.dateFOA2021-06-09T06:47:12Z


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