2016
DOI: 10.1039/c6sc00563b
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Long-afterglow metal–organic frameworks: reversible guest-induced phosphorescence tunability

Abstract: We report that two types of Zn-terephthalate (TPA) MOFs (namely [Zn(TPA)(DMF)] (1-DMF) and MOF-5) could exhibit an obvious room-temperature afterglow emission with a time-resolved luminescence lifetime as high as 0.47 seconds.

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Cited by 412 publications
(254 citation statements)
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“…31 The resulting host–guest nanohybrid materials exhibited long-lived green RTP (Fig. 2a, afterglow time range: 0–6 seconds), showing that formation of 2D intercalation nanohybrids is indeed a feasible alternative to crystallization as a means of increasing the phosphorescence lifetimes of such simple organic species.…”
Section: Introductionmentioning
confidence: 93%
“…31 The resulting host–guest nanohybrid materials exhibited long-lived green RTP (Fig. 2a, afterglow time range: 0–6 seconds), showing that formation of 2D intercalation nanohybrids is indeed a feasible alternative to crystallization as a means of increasing the phosphorescence lifetimes of such simple organic species.…”
Section: Introductionmentioning
confidence: 93%
“…One is to facilitatie the intersystem crossing (ISC) from the lowest excited singlet state (S 1 ) to a triplet state (T n ) to populate the triplet excitons, and the other is to inhibit non‐radiative transitions from the lowest excited triplet state (T 1 ) to the ground state (S 0 ). On the basic of these factors, researchers have proposed various strategies and methods to moldulate phosphorescent performance, such as intruduction of heavy atoms, heteroatoms and aromatic carbony to boost SOC; while suppressing non‐radiation of the triplet excitons by host‐guest doping method crystalization and organic flameworks . Therefore, developing metal‐free organic luminescent materials with highly efficient room temperature phosphorescence has been becoming a hot topic in recent years …”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5][6][7][8][9][10][11][12] However,achieving RTPmaterials is agreat challenge owing to the spin-forbidden nature of triplet exciton transitions.T od ate,R TP materials are still mainly limited to organometallic complexes and metal-free pure organic compounds, [1,2,11,[13][14][15][16] but all of them suffer from high cost and toxicity,s ensitivity to atmospheric oxygen, complicated preparation, and/or observable only in the crystalline/composite forms. [4,17] Therefore,itisstill highly desirable to develop novel RTPm aterials that featuring facile and quick preparation, are metal-free,have long lifetime,are cost effective,and have low toxicity. [4,17] Therefore,itisstill highly desirable to develop novel RTPm aterials that featuring facile and quick preparation, are metal-free,have long lifetime,are cost effective,and have low toxicity.…”
mentioning
confidence: 99%