Microwave-assisted synthesis of defective Ca 1- x Ag x Ti 1- y Co y O 3 with high photoelectrocatalytic activity for organic pollutant removal from water

CaTiO is considered to be one of the most promising catalysts for the degradation of organic pollutants, but its application is limited by the wide band gap and low catalytic activity. Element doping is an effective strategy to solve these problems. Herein, a novel CaTiO co-doped with Ag and Co (Ca...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2022-02, Vol.51 (6), p.2219-2225
Hauptverfasser: Chen, Chen, Zhao, Jiamei, Guo, Dong, Duan, Keyu, Wang, Yongqiang, Lun, Xiaowen, Zhang, Conglu
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Sprache:eng
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Zusammenfassung:CaTiO is considered to be one of the most promising catalysts for the degradation of organic pollutants, but its application is limited by the wide band gap and low catalytic activity. Element doping is an effective strategy to solve these problems. Herein, a novel CaTiO co-doped with Ag and Co (Ca Ag Ti Co O ) was synthesized by combining co-precipitation and the microwave hydrothermal method for the first time. The crystal structure, microstructure and light absorption of the material were systematically investigated. The results showed that Ca Ag Ti Co O had higher light absorption than pure CaTiO , and the band gap was reduced to 2.78 eV. First-principles calculations indicated that Ag-Ca and Co-Ti tended to form donor-acceptor defect pairs in the doping process. These defect states not only enhanced the adsorption properties, but also could be used as carrier traps to optimize the dielectric properties of CaTiO . In the photoelectrocatalytic system, with 0.01 g of catalyst, 98% of methylene blue in 100 mL solution (10 mg L ) was degraded in 150 min. In addition, Ca Ag Ti Co O showed strong stability and excellent recyclability. The double ion co-doping technology will provide an effective strategy for improving the catalytic activity of traditional wide-band gap semiconductors.
ISSN:1477-9226
1477-9234
DOI:10.1039/D1DT03894J