Achievement of intrinsic white light emission by hybridization-deformable haloplumbates with rigid luminescent naphthalene motifs. Issue 22 (19th October 2020)

• Record Type: Journal Article
• Authors: Lin, Xiang-Ling; Chen, Bin; Huang, You-Ren; Song, Kai-Yue; Zhou, Pan-Ke; Zong, Lu-Lu; Li, Hao-Hong; Chen, Zhi-Rong; Jiang, Rong
• Is Part Of: Inorganic chemistry frontiers. Volume 7:Issue 22(2020)
• Page Start: 4477
• Page End: 4487
• Publication Date: 2020-10-19
• Subjects: Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d0qi00995d
• Languages: English
• ISSNs: 2052-1553

Abstract

Abstract : The combination of red emissions stemming from deformable haloplumbates and blue emissions originating from luminescent naphthalene motifs give rise to intrinsic single-component white-light emitters. Abstract : The design of single-component broadband photoemitters with high stability is imperative for the development of next-generation WLEDs. In this work, 1D cationic haloplumbate chains and rigid luminescent naphthalene dicarboxylate (2, 6-ndc) with a larger conjugated system were used to construct crystalline single-component broadband photoemitters, i.e. formulated as [(Pb4 X2 )(ndc)4 ·A2 ] n (X = Cl, Br, and I, A = (CH3 )3 NH + and (CH3 )2 NH2 + ). These hybrids are 3D networks built from flexible 1D cationic (Pb4 X2 ) 6+ chains and rigid 2, 6-naphthalene dicarboxylic acid ligands. The variation of halogen atoms from Cl to Br/I with higher polarity can switch the holo-directed geometry to the hemi-directed geometry with different distorted degrees. The larger conjugated system of 2, 6-ndc leads to strong individual blue adsorptions and emissions. In particular, the Br- and I-analogues with hemi-directed geometries can give rise to additional red emissions, corresponding to the presence of stereochemical activities of Pb centers. Consequently, Br- and I-analogues are white-light emitters containing red emissions stemming from deformable haloplumbate and blue emissions originating from luminescent naphthalene motifs. Interestingly, haloplumbate-based emissions are thermally tunable, and those of naphthalene are generally inactive to thermal stimulus. As a result, tunable emissions from blue/white to yellow can be achieved. The higher quantum yield of Br-analogues can be assigned to their worse haloplumbate connectivity, which can enhance the electron–phonon coupling. In all, the combination of flexible haloplumbate chains with larger π-conjugated fluorophores is an efficient strategy for the construction of tunable broadband photoemitters.