Synthesis and CO2 photoreduction of two 3d-4f heterometal-organic frameworks

被引:2
作者
Yang, Yu [1 ]
Fu, Yaomei [2 ]
You, Siqi [1 ]
Li, Mingyue [1 ]
Qin, Chao [1 ]
Zhao, Liang [1 ]
Su, Zhongmin [1 ]
机构
[1] Northeast Normal Univ, Key Lab Polyoxometalate & Reticular Mat Chem, Minist Educ, Changchun 130024, Jilin, Peoples R China
[2] Weifang Univ Sci & Technol, Shandong Peninsula Engn Res Ctr Comprehens Brine, Shouguang 262700, Peoples R China
基金
中国国家自然科学基金;
关键词
CARBON-DIOXIDE; CATALYST; REDUCTION; CAPTURE;
D O I
10.1039/d1nj03479k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two 3d-4f heterometal-organic frameworks are synthesized by a steam-assisted conversion method and are characterized by single-crystal X-ray diffraction, PXRD, IR, TG, and UV-vis spectroscopy. Compounds 1 and 2 have similar structures, in which binuclear gadolinium clusters are connected by [M(BPDC)(3)] (M = Ni for 1 and Co for 2) secondary building units (SBUs) and extend into 3D frameworks with pcu topologies. In addition, we have also investigated the photoreduction of CO2 under visible light. The CO yields reached 7622 mu mol(-1) g(-1) and 11 250 mu mol(-1) g(-1) with 1 and 2 as catalysts, respectively, and ruthenium pyridine as the photosensitizer after two hours of visible light irradiation. Both of them have high selectivity values for CO, reaching 94.85% for 1 and 94.46% for 2. Furthermore, the catalytic mechanism is proposed through a photoelectrochemical test. This study provides a feasible strategy for the design of efficient CO2 photocatalysts with a high charge separation rate.
引用
收藏
页码:18790 / 18795
页数:6
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