BiOBr as template and Bi.sup.3+ source to support the growth of Bi-Zn bimetallic MOF and hybrid photocatalysts with highly visible-light photocatalytic performances

Two affordable ligands of H.sub.3BTC and 1,10-phen were used to synthesize novel metal organic frameworks (Bi-Zn MOF, named as HPBZ) and BiOBr/Bi-ZnMOF (named as HPBOBZ) composites as photocatalysts removing RhB by introducing Bi-Zn bimetals and changing the reaction conditions (ligand molar ratio,...

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Bibliographic Details
Published in:	Journal of materials science 2023-02, Vol.58 (6), p.2506
Main Authors:	Lou, Weiyi, Wang, Liying, Cao, Zhenzhu, Zhang, Yongfeng, Yang, Jucai, Cheng, Lin
Format:	Article
Language:	eng
Subjects:	Methylene blue Zinc compounds
Online Access:	Get full text
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Summary:	Two affordable ligands of H.sub.3BTC and 1,10-phen were used to synthesize novel metal organic frameworks (Bi-Zn MOF, named as HPBZ) and BiOBr/Bi-ZnMOF (named as HPBOBZ) composites as photocatalysts removing RhB by introducing Bi-Zn bimetals and changing the reaction conditions (ligand molar ratio, pH, reaction time, and temperature). Bi-Zn MOF exhibited well stability in the cyclic photocatalytic experiments. The synergy between Bi.sup.3+-Zn.sup.2+ improves the structural stability of the framework. The introduction of 1,10-phen not only increases the pore size but also realizes the modification of the bandgap, thereby enhancing the light response range and further improving the effect of photocatalytic activity. For BiOBr/Bi-Zn MOF hybrid photocatalysts, the BiOBr was Bi.sup.3+ source to grow Bi-Zn MOF in situ, and it enhanced highly visible-light photocatalytic performances with significant stability (The degradation efficiency still maintains 97.8% after three cycles) in the decomposition of RhB. The degradation efficiency reached 99% under visible light irradiation for 20 min. The integration of Bi-Zn hybrid metal-organic frameworks with BiOBr semiconductors provides a new perspective on developing heterojunction catalysts for environmental remediation.
ISSN:	0022-2461 1573-4803