Anions mediated amino-type Cd-MOFs catalysts for efficient photocatalytic hydrogen evolution

Photocatalytic water splitting can be used to directly transfer solar energy into chemical energy with highly efficiency. Metal-organic frameworks (MOFs) materials are well known on the advantages of high design flexibility and metal center functionalization. In this study, a series of Cd-centered M...

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Published inJournal of solid state chemistry Vol. 304; p. 122632
Main Authors Qian, Jun-Feng, Yue, Hua-Dong, Qiu, Peng-Xiang, Liang, Qian, Hang, Meng-Ting, He, Ming-Yang, Bu, Yun-Fei, Chen, Qun, Zhang, Zhi-Hui
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LanguageEnglish
Published Elsevier Inc 01.12.2021
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Abstract Photocatalytic water splitting can be used to directly transfer solar energy into chemical energy with highly efficiency. Metal-organic frameworks (MOFs) materials are well known on the advantages of high design flexibility and metal center functionalization. In this study, a series of Cd-centered MOFs were successfully fabricated by a simple solvent evaporation method based on the different anion mediated pyridyl leucine derivatives. Single-crystal X-Ray diffraction showed the isostructural 3D chiral coordination networks of three Cd-MOFs with helical chains connected by the adjacent carboxylate groups. Within the helical coordination chains, the formate (For) and acetate (OAc) anions adopted chelate modes in Cd-LFor and Cd-LOAc, whereas the chloride worked as a monodetate ligand in Cd-LCl. Powder X-ray diffraction (PXRD), Thermogravimetric analysis, UV–vis spectra, Photocurrent-time test (I-t) and Mott-Schottky (MS) curves were carried out to characterize and analysis these Cd-MOFs. All the samples exhibit photocatalytic activity for hydrogen generation in aqueous solution of Na2S/Na2SO3 upon irradiation at full light. The photocurrent time test showed that Cd-LCl showed a higher photocurrent intensity than those of Cd-LFor and Cd-LOAc, which proved the lower electron-hole recombination and correspondingly higher hydrogen production photocatalysis active. The highest H2 production rate reached 17242 ​μmol ​g−1 ​h−1 for Cd-LCl. In the photocatalytic reaction, the hydrogen production rate was stable without significant decrease, indicating that the material had no significant deactivation and had good photocatalytic activity. Novel anion mediated amino-type Cd-MOFs exhibit photocatalytic activity for hydrogen generation in aqueous solution with Na2S/Na2SO3 as the sacrificial agents upon irradiation at full light, in which amino and chloride promote the photocatalysis performance. [Display omitted] •Novel anion mediated amino-type Cd-MOFs were synthesized and adopted unique 3D coordination network with solvent channels.•All the Cd-MOFs exhibit photocatalytic activity for hydrogen generation in aqueous solution upon irradiation at full light.•The amino group and the doping chloride led to good photocatalytic water splitting performance of Cd-LCl.
AbstractList Photocatalytic water splitting can be used to directly transfer solar energy into chemical energy with highly efficiency. Metal-organic frameworks (MOFs) materials are well known on the advantages of high design flexibility and metal center functionalization. In this study, a series of Cd-centered MOFs were successfully fabricated by a simple solvent evaporation method based on the different anion mediated pyridyl leucine derivatives. Single-crystal X-Ray diffraction showed the isostructural 3D chiral coordination networks of three Cd-MOFs with helical chains connected by the adjacent carboxylate groups. Within the helical coordination chains, the formate (For) and acetate (OAc) anions adopted chelate modes in Cd-LFor and Cd-LOAc, whereas the chloride worked as a monodetate ligand in Cd-LCl. Powder X-ray diffraction (PXRD), Thermogravimetric analysis, UV–vis spectra, Photocurrent-time test (I-t) and Mott-Schottky (MS) curves were carried out to characterize and analysis these Cd-MOFs. All the samples exhibit photocatalytic activity for hydrogen generation in aqueous solution of Na2S/Na2SO3 upon irradiation at full light. The photocurrent time test showed that Cd-LCl showed a higher photocurrent intensity than those of Cd-LFor and Cd-LOAc, which proved the lower electron-hole recombination and correspondingly higher hydrogen production photocatalysis active. The highest H2 production rate reached 17242 ​μmol ​g−1 ​h−1 for Cd-LCl. In the photocatalytic reaction, the hydrogen production rate was stable without significant decrease, indicating that the material had no significant deactivation and had good photocatalytic activity. Novel anion mediated amino-type Cd-MOFs exhibit photocatalytic activity for hydrogen generation in aqueous solution with Na2S/Na2SO3 as the sacrificial agents upon irradiation at full light, in which amino and chloride promote the photocatalysis performance. [Display omitted] •Novel anion mediated amino-type Cd-MOFs were synthesized and adopted unique 3D coordination network with solvent channels.•All the Cd-MOFs exhibit photocatalytic activity for hydrogen generation in aqueous solution upon irradiation at full light.•The amino group and the doping chloride led to good photocatalytic water splitting performance of Cd-LCl.
ArticleNumber 122632
Author Chen, Qun
Liang, Qian
Qiu, Peng-Xiang
Hang, Meng-Ting
Qian, Jun-Feng
Zhang, Zhi-Hui
He, Ming-Yang
Bu, Yun-Fei
Yue, Hua-Dong
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  email: zhangzh@cczu.edu.cn
  organization: Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Advanced Catalysis and Green Manufacturing Collaborative Innovation Center, Changzhou University, Changzhou, 213164, China
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Keywords Amino acids
Weak coordinated anions
Metal-organic frameworks
Photocatalysis
Hydrogen production
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Snippet Photocatalytic water splitting can be used to directly transfer solar energy into chemical energy with highly efficiency. Metal-organic frameworks (MOFs)...
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elsevier
SourceType Enrichment Source
Index Database
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StartPage 122632
SubjectTerms Amino acids
Hydrogen production
Metal-organic frameworks
Photocatalysis
Weak coordinated anions
Title Anions mediated amino-type Cd-MOFs catalysts for efficient photocatalytic hydrogen evolution
URI https://dx.doi.org/10.1016/j.jssc.2021.122632
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