Cobalt Hydrogen-Bonded Organic Framework as a Visible Light-Driven Photocatalyst for CO2 Cycloaddition Reaction

被引:25
|
作者
Siddig, Lamia A. [1 ]
Alzard, Reem H. [1 ]
Abdelhamid, Abdalla S. [1 ,2 ]
Ramachandran, Tholkappiyan [3 ]
Nguyen, Ha L. [4 ]
Paz, Alejandro Perez [1 ]
Alzamly, Ahmed [1 ]
机构
[1] UAE Univ, Dept Chem, Al Ain 15551, U Arab Emirates
[2] UAE Univ, Dept Chem Engn, Al Ain 15551, U Arab Emirates
[3] UAE Univ, Dept Phys, Al Ain 15551, U Arab Emirates
[4] Univ Calif Berkeley, Berkeley Global Sci Inst, Berkeley, CA 94720 USA
关键词
CYCLIC CARBONATES; EPOXIDES; CONSTRUCTION; CONVERSION; CRYSTAL; DIOXIDE; HOFS;
D O I
10.1021/acs.inorgchem.3c02051
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A novel cobalt hydrogen-bonded organic framework (Co-HOF, C24H14CoN4O8) was synthesized from a mixed linker, that is, 2,5-pyridinedicarboxylic acid (PDC) and 2,2'-bipyridyl (BPY) linkers and cobalt ion through a simple, one-pot, low-cost, and scalable solvothermal method. The Co-HOF was fully characterized using several analytical and spectroscopic techniques including single-crystal X-ray diffraction, diffuse reflectance spectroscopy, Fourier transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray, and X-ray photoelectron spectroscopy. The Co-HOF exhibits high thermal and chemical stabilities compared to previously reported HOF materials. Moreover, Co-HOF shows excellent photocatalytic activity under visible light irradiation due to its narrow band gap of 2.05 eV. The cycloaddition reaction of CO2 to variable epoxides was investigated to evaluate the photocatalytic performance of Co-HOF under visible light radiation and was found to produce the corresponding cyclic carbonates in yields up to 99.9%.
引用
收藏
页码:15550 / 15564
页数:15
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