fiamtyu@nwpu.edu.cn
giamzfan@njtech.edu.cn
hvc@nwpu.edu.cn
收稿日期:2023-11-22,
修回日期:2024-02-28,
录用日期:2024-03-11,
网络出版日期:2024-04-08,
纸质出版日期:2024-12
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Dual-channel mechano-phosphorescence: a combined locking effect with twisted molecular structures and robust interactions[J]. LSA, 2024,13(4):738-746.
Zongliang Xie, Zhu Mao, Hailan Wang, et al. Dual-channel mechano-phosphorescence: a combined locking effect with twisted molecular structures and robust interactions[J]. Light: science & applications, 2024, 13(4): 738-746.
Dual-channel mechano-phosphorescence: a combined locking effect with twisted molecular structures and robust interactions[J]. LSA, 2024,13(4):738-746. DOI: 10.1038/s41377-024-01421-5.
Zongliang Xie, Zhu Mao, Hailan Wang, et al. Dual-channel mechano-phosphorescence: a combined locking effect with twisted molecular structures and robust interactions[J]. Light: science & applications, 2024, 13(4): 738-746. DOI: 10.1038/s41377-024-01421-5.
Organic mechanoluminescence materials
featuring dual emission and ultralong phosphorescence characteristics
exhibit significant potential for applications in real-time stress sensing
pressure-sensitive lighting
advanced security marking techniques
and material breakage monitoring. However
due to immature molecular design strategies and unclear luminescence mechanisms
these materials remain rarely reported. In this study
we propose a valuable molecular design strategy to achieve dual-channel mechano-phosphorescence. By introducing the arylphosphine oxide group into a highly twisted molecular framework
enhanced intra- and intermolecular interactions could be achieved within rigid structures
leading to dual-channel mechanoluminescence with greatly promoted ultralong phosphorescence. Further investigations reveal the substantial boosting effect of intra- and intermolecular interactions on mechanoluminescence and ultralong phosphorescence properties by locking the highly twisted molecular skeleton. This work provides a concise and guiding route to develop novel smart responsive luminescence materials for widespread applications in material science.
Dual-channel mechano-phosphorescence
characterized by dual emission and ultralong organic phosphorescence
was achieved by strengthening the intra- and intermolecular interactions in the highly twisted structures to realize a combined locking effect.
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Y.J. Xie , Z. Li , Triboluminescence: recalling interest and new aspects . Chem 4 , 943 - 971 ( 2018 ). http://doi.org/10.1016/j.chempr.2018.01.001 http://doi.org/10.1016/j.chempr.2018.01.001
S. Mukherjee , P. Thilagar , Renaissance of organic triboluminescent materials . Angew. Chem. Int. Ed. 58 , 7922 - 7932 ( 2019 ). http://doi.org/10.1002/anie.201811542 http://doi.org/10.1002/anie.201811542
C.G. Camara et al. , Correlation between nanosecond X-ray flashes and stick–slip friction in peeling tape . Nature 455 , 1089 - 1092 ( 2008 ). http://doi.org/10.1038/nature07378 http://doi.org/10.1038/nature07378
N.C. Eddingsaas , K.S. Suslick , Light from sonication of crystal slurries . Nature 444 , 163 - 163 ( 2006 ). http://doi.org/10.1038/444163a http://doi.org/10.1038/444163a
Z.F. Huang et al. , Smart mechanoluminescent phosphors: a review of strontium-aluminate-based materials, properties, and their advanced application technologies . Adv. Sci. 10 , 2204925 ( 2023 ). http://doi.org/10.1002/advs.202204925 http://doi.org/10.1002/advs.202204925
Y.X. Zhuang , R.J. Xie , Mechanoluminescence rebrightening the prospects of stress sensing: a review . Adv. Mater. 33 , 2005925 ( 2021 ). http://doi.org/10.1002/adma.202005925 http://doi.org/10.1002/adma.202005925
Z.L. Xie et al. , Realizing photoswitchable mechanoluminescence in organic crystals based on photochromism . Adv. Mater. 35 ,( 2023 ). http://doi.org/10.1002/adma.202212273 http://doi.org/10.1002/adma.202212273
B. Hou et al. , An interactive mouthguard based on mechanoluminescence-powered optical fibre sensors for bite-controlled device operation . Nat. Electron. 5 , 682 - 693 ( 2022 ). http://doi.org/10.1038/s41928-022-00841-8 http://doi.org/10.1038/s41928-022-00841-8
S.M. Jeong et al. , Bright, wind-driven white mechanoluminescence from zinc sulphide microparticles embedded in a polydimethylsiloxane elastomer . Energy Environ. Sci. 7 , 3338 - 3346 ( 2014 ). http://doi.org/10.1039/C4EE01776E http://doi.org/10.1039/C4EE01776E
Y. Hirai et al. , Triboluminescence of lanthanide coordination polymers with face-to-face arranged substituents . Angew. Chem. Int. Ed. 56 , 7171 - 7175 ( 2017 ). http://doi.org/10.1002/anie.201703638 http://doi.org/10.1002/anie.201703638
X. Qian et al. , Printable skin-driven mechanoluminescence devices via nanodoped matrix modification . Adv. Mater. 30 ,( 2018 ). http://doi.org/10.1002/adma.201800291 http://doi.org/10.1002/adma.201800291
D. Peng et al. , A ZnS/CaZnOS heterojunction for efficient mechanical-to-optical energy conversion by conduction band offset . Adv. Mater. 32 ,( 2020 ). http://doi.org/10.1002/adma.201907747 http://doi.org/10.1002/adma.201907747
G.E. Hardy et al. , Triboluminescence spectroscopy of aromatic compounds . J. Am. Chem. Soc. 99 , 3552 - 3558 ( 1977 ). http://doi.org/10.1021/ja00453a002 http://doi.org/10.1021/ja00453a002
B.J. Xu et al. , Very bright mechanoluminescence and remarkable mechanochromism using a tetraphenylethene derivative with aggregation-induced emission . Chem. Sci. 6 , 3236 - 3241 ( 2015 ). http://doi.org/10.1039/C5SC00466G http://doi.org/10.1039/C5SC00466G
C. Wang et al. , A stable tetraphenylethene derivative: aggregation-induced emission, different crystalline polymorphs, and totally different mechanoluminescence properties . Mater. Horiz. 3 , 220 - 225 ( 2016 ). http://doi.org/10.1039/C6MH00025H http://doi.org/10.1039/C6MH00025H
J. Yang et al. , AIEgen with fluorescence-phosphorescence dual mechanoluminescence at room temperature . Angew. Chem. Int. Ed. 56 , 880 - 884 ( 2017 ). http://doi.org/10.1002/anie.201610453 http://doi.org/10.1002/anie.201610453
Q.K. Sun et al. , Bright NUV mechanofluorescence from a terpyridine-based pure organic crystal . Chem. Commun. 54 , 94 - 97 ( 2018 ). http://doi.org/10.1039/C7CC08064F http://doi.org/10.1039/C7CC08064F
J.A. Li et al. , Transient and persistent room-temperature mechanoluminescence from a white-light-emitting AIEgen with tricolor emission switching triggered by light . Angew. Chem. Int. Ed. 57 , 6449 - 6453 ( 2018 ). http://doi.org/10.1002/anie.201800762 http://doi.org/10.1002/anie.201800762
H. Nakayama et al. , Crystal structures and triboluminescence based on trifluoromethyl and pentafluorosulfanyl substituted asymmetric N -phenyl imide compounds . Chem. Mater. 24 , 671 - 676 ( 2012 ). http://doi.org/10.1021/cm202650u http://doi.org/10.1021/cm202650u
J.I. Nishida et al. , Phthalimide compounds containing a trifluoromethylphenyl group and electron-donating aryl groups: color-tuning and enhancement of triboluminescence . J. Org. Chem. 81 , 433 - 441 ( 2016 ). http://doi.org/10.1021/acs.joc.5b02191 http://doi.org/10.1021/acs.joc.5b02191
G.E. Hardy et al. , Structure and triboluminescence of polymorphs of hexaphenylcarbodiphosphorane . J. Am. Chem. Soc. 100 , 8001 - 8002 ( 1978 ). http://doi.org/10.1021/ja00493a035 http://doi.org/10.1021/ja00493a035
Z.L. Xie et al. , Weak interactions but potent effect: tunable mechanoluminescence by adjusting intermolecular C-H⋯π interactions . Chem. Sci. 9 , 5787 - 5794 ( 2018 ). http://doi.org/10.1039/C8SC01703D http://doi.org/10.1039/C8SC01703D
J. Yang et al. , Elucidating the excited state of mechanoluminescence in organic luminogens with room-temperature phosphorescence . Angew. Chem. Int. Ed. 56 , 15299 - 15303 ( 2017 ). http://doi.org/10.1002/anie.201708119 http://doi.org/10.1002/anie.201708119
K.K. Neena et al. , Diarylboryl-phenothiazine based multifunctional molecular siblings . Chem. Commun. 53 , 3641 - 3644 ( 2017 ). http://doi.org/10.1039/C6CC09717K http://doi.org/10.1039/C6CC09717K
E. Lucenti et al. , H-aggregates granting crystallization-induced emissive behavior and ultralong phosphorescence from a pure organic molecule . J. Phys. Chem. Lett. 8 , 1894 - 1898 ( 2017 ). http://doi.org/10.1021/acs.jpclett.7b00503 http://doi.org/10.1021/acs.jpclett.7b00503
Z.F. An et al. , Stabilizing triplet excited states for ultralong organic phosphorescence . Nat. Mater. 14 , 685 - 690 ( 2015 ). http://doi.org/10.1038/nmat4259 http://doi.org/10.1038/nmat4259
Z.K. He et al. , White light emission from a single organic molecule with dual phosphorescence at room temperature . Nat. Commun. 8 ,( 2017 ). http://doi.org/10.1038/s41467-017-00362-5 http://doi.org/10.1038/s41467-017-00362-5
Z. Yang et al. , Boosting the quantum efficiency of ultralong organic phosphorescence up to 52% via intramolecular halogen bonding . Angew. Chem. Int. Ed. 59 , 17451 - 17455 ( 2020 ). http://doi.org/10.1002/anie.202007343 http://doi.org/10.1002/anie.202007343
Z.Y. Zhang , Y. Liu , Ultralong room-temperature phosphorescence of a solid-state supramolecule between phenylmethylpyridinium and cucurbit[6]uril . Chem. Sci. 10 , 7773 - 7778 ( 2019 ). http://doi.org/10.1039/C9SC02633A http://doi.org/10.1039/C9SC02633A
Y.Y. Gong et al. , Achieving persistent room temperature phosphorescence and remarkable mechanochromism from pure organic luminogens . Adv. Mater. 27 , 6195 - 6201 ( 2015 ). http://doi.org/10.1002/adma.201502442 http://doi.org/10.1002/adma.201502442
O. Bolton et al. , Activating efficient phosphorescence from purely organic materials by crystal design . Nat. Chem. 3 , 205 - 210 ( 2011 ). http://doi.org/10.1038/nchem.984 http://doi.org/10.1038/nchem.984
Z.Y. Yang et al. , Intermolecular electronic coupling of organic units for efficient persistent room-temperature phosphorescence . Angew. Chem. Int. Ed. 55 , 2181 - 2185 ( 2016 ). http://doi.org/10.1002/anie.201509224 http://doi.org/10.1002/anie.201509224
R. Kabe , C. Adachi , Organic long persistent luminescence . Nature 550 , 384 - 387 ( 2017 ). http://doi.org/10.1038/nature24010 http://doi.org/10.1038/nature24010
J.R. Chen et al. , Achieving dual-emissive and time-dependent evolutive organic afterglow by bridging molecules with weak intermolecular hydrogen bonding . Adv. Opt. Mater. 7 ,( 2019 ). http://doi.org/10.1002/adom.201801593 http://doi.org/10.1002/adom.201801593
K. Ling et al. , Controllable multiemission with ultralong organic phosphorescence in crystal by isomerization . Adv. Opt. Mater. 7 ,( 2019 ). http://doi.org/10.1002/adom.201901076 http://doi.org/10.1002/adom.201901076
L. Gu et al. , Dynamic ultralong organic phosphorescence by photoactivation . Angew. Chem. Int. Ed. 57 , 8425 - 8431 ( 2018 ). http://doi.org/10.1002/anie.201712381 http://doi.org/10.1002/anie.201712381
Y. Liu et al. , Robust white-light emitting and multi-responsive luminescence of a dual-mode phosphorescence molecule . Adv. Opt. Mater. 9 ,( 2021 ). http://doi.org/10.1002/adom.202001685 http://doi.org/10.1002/adom.202001685
X.P. Zhang et al. , Ultralong UV/mechano-excited room temperature phosphorescence from purely organic cluster excitons . Nat. Commun. 10 ,( 2019 ). http://doi.org/10.1038/s41467-019-13048-x http://doi.org/10.1038/s41467-019-13048-x
S. Biju et al. , Brilliant photoluminescence and triboluminescence from ternary complexes of Dy III and Tb III with 3-phenyl-4-propanoyl-5-isoxazolonate and a bidentate phosphine oxide coligand . Inorg. Chem. 52 , 8750 - 8758 ( 2013 ). http://doi.org/10.1021/ic400913f http://doi.org/10.1021/ic400913f
B.P. Chandra , J.I. Zink , Triboluminescence of crystals containing the triphenyl group . J. Phys. Chem. 86 , 4138 - 4141 ( 1982 ). http://doi.org/10.1021/j100218a009 http://doi.org/10.1021/j100218a009
X.L. Yang , G.J. Zhou , W.Y. Wong , Functionalization of phosphorescent emitters and their host materials by main-group elements for phosphorescent organic light-emitting devices . Chem. Soc. Rev. 44 , 8484 - 8575 ( 2015 ). http://doi.org/10.1039/C5CS00424A http://doi.org/10.1039/C5CS00424A
G.J. Zhou et al. , Manipulating charge-transfer character with electron-withdrawing main-group moieties for the color tuning of iridium electrophosphors . Adv. Funct. Mater. 18 , 499 - 511 ( 2008 ). http://doi.org/10.1002/adfm.200700719 http://doi.org/10.1002/adfm.200700719
G.J. Zhou et al. , Metallophosphors of platinum with distinct main-group elements: a versatile approach towards color tuning and white-light emission with superior efficiency/color quality/brightness trade-offs . J. Mater. Chem. 20 , 7472 - 7484 ( 2010 ). http://doi.org/10.1039/c0jm01159b http://doi.org/10.1039/c0jm01159b
X.Y. Liu et al. , Novel o -D-π-A arylamine/arylphosphine oxide hybrid hosts for efficient phosphorescent organic light-emitting diodes . Org. Electron. 56 , 186 - 191 ( 2018 ). http://doi.org/10.1016/j.orgel.2018.02.021 http://doi.org/10.1016/j.orgel.2018.02.021
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