Efficient External Electric Field Manipulated Nonlinear Optical Switches of All-Metal Electride Molecules with Infrared transparency: Nonbonding Electron Transfer Forms an Excess Electron Lone Pair
dc.contributor.author
dc.date.accessioned
2019-05-07T10:32:50Z
dc.date.available
2019-05-07T10:32:50Z
dc.date.issued
2017-01-12
dc.identifier.issn
1932-7447
dc.identifier.uri
dc.description.abstract
Focusing on the interesting new concept of all-metal electride, centrosymmetric molecules e^− + M^(2+) (Ni@Pb_12)^(2−) M^(2+) + e^− (M = Be, Mg, and Ca) with two anionic excess electrons located at the opposite ends of the molecule are obtained theoretically. These novel molecular all-metal electrides can act as infrared (IR) nonlinear optical (NLO) switches. Whereas the external electric field (F) hardly changes the molecular structure of the all-metal electrides, it seriously deforms their excess electron orbitals and average static first hyperpolarizabilities (β0 e (F)). For e^− + Ca^(2+) (Ni@Pb_12)^(2−) Ca^(2+) + e^−, a small external electric field F = 8 × 10−4 au (0.04 V/Å) drives a long-range excess electron transfer from one end of the molecule through the middle all-metal anion cage (Ni@Pb_12)^(2−) to the other end. This long-range electron transfer is shown by a prominent change of excess electron orbital from double lobes to single lobe, which forms an excess electron lone pair and electronic structure Ca^(2+) (Ni@Pb_12)^(2−) Ca^(2+) + 2e^−. Therefore, the small external electric field induces a dramatic β_0 e (F) contrast from 0 (off form) to 2.2 × 106 au (on form) in allmetal electride molecule Ca(Ni@Pb_12)Ca. Obviously, such switching is high sensitive. Interestingly, in the switching process, such long-range excess electron transfer does not alter the valence and chemical bond nature. Then, this switching mechanism is a distinct nonbonding evolution named electronic structure isomerization, which means that such switching has the advantages of being fast and reversible. Besides, these all-metal electride molecules also have a rare IR transparent characteristic (1.5−10 μm) in NLO electride molecules, and hence are commendable molecular IR NLO switches. Therefore, this work opens a new research field of electric field manipulated IR NLO switches of molecular all-metal electrides
dc.description.sponsorship
This study was supported by the National Natural Science Foundation of China (Grant
Nos. 21573089, 21303066, 21173095, 21403083, 21603082, 21403075, 21673085),
the State Key Development Program for Basic Research of China (Grant No.
2013CB834801), the Graduate Innovation Fund of Jilin University (Grant No.
2016158), the Spanish Ministerio de Economıa y competividad (MINECO,
CTQ2014-52525-P) and the Generalitat de Catalunya (project number 2014SGR931)
dc.format.extent
11 p.
dc.format.mimetype
application/pdf
dc.language.iso
eng
dc.publisher
American Chemical Society (ACS)
dc.relation
info:eu-repo/grantAgreement/MINECO//CTQ2014-52525-P/ES/FUNCIONALES DFT PARA EL CALCULO DE PROPIEDADES OPTICAS NO LINEALES/
dc.relation.isformatof
Versió postprint del document publicat a: https://doi.org/10.1021/acs.jpcc.6b11919
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© Journal of Physical Chemistry C, 2017, vol. 121, núm. 1, p. 958-968
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Articles publicats (D-Q)
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Tots els drets reservats
dc.source
He, Hui-Min Li, Ying Yang, Hui Yu, Dan Li, Si-Yi Wu, Di Hou, Jian-Hua Zhong, Rong-Lin Zhou, Zhong-Jun Gu, Feng-Long Luis Luis, Josep Maria Li, Zhi-Ru 2017 Efficient External Electric Field Manipulated Nonlinear Optical Switches of All-Metal Electride Molecules with Infrared transparency: Nonbonding Electron Transfer Forms an Excess Electron Lone Pair Journal of Physical Chemistry C 121 1 958 968
dc.title
Efficient External Electric Field Manipulated Nonlinear Optical Switches of All-Metal Electride Molecules with Infrared transparency: Nonbonding Electron Transfer Forms an Excess Electron Lone Pair
dc.type
info:eu-repo/semantics/article
dc.rights.accessRights
info:eu-repo/semantics/openAccess
dc.type.version
info:eu-repo/semantics/acceptedVersion
dc.identifier.doi
dc.identifier.idgrec
026357
dc.contributor.funder
dc.type.peerreviewed
peer-reviewed
dc.relation.ProjectAcronym
dc.identifier.eissn
1932-7455