Unlocking the Potential of Cobalt-Based Metal-Organic Frameworks for Alkaline Oxygen Evolution and One-Pot Synthesis of Styrene Carbonate from Styrene and Carbon Dioxide

被引:0
|
作者
Rana, Abhijeet [1 ]
Karmakar, Arun [2 ]
Kundu, Subrata [2 ]
Biswas, Shyam [1 ]
机构
[1] Indian Inst Technol Guwahati, Dept Chem, Gauhati 781039, Assam, India
[2] CSIR Cent Electrochem Res Inst CECRI, Mat Chem Lab Energy Environm & Catalysis, Electrochem Proc Engn EPE Div, Karaikkudi 630003, Tamil Nadu, India
关键词
BIFUNCTIONAL ELECTROCATALYSTS; HYDROGEN GENERATION; EFFICIENT; REDUCTION; DESIGN; OER;
D O I
10.1021/acs.inorgchem.5c00013
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This work presents the synthesis of a Co(II) MOF, IITG-7, with a 5-(((1H-imidazole-2-yl)methyl)amino)isophthalic acid linker using a solvothermal method. The activated MOF IITG-7a demonstrates excellent performance for the oxygen evolution reaction (OER) in an alkaline medium, requiring only 350 mV overpotential to achieve a 10 mA/cm2 current density, along with a minimal Tafel slope of 55.2 mV/dec and a charge transfer resistance of 3.5 Omega. Additionally, IITG-7a was successfully applied as a catalyst for the direct synthesis of styrene carbonate (SC) from styrene and CO2, achieving 100% conversion in the presence of tert-butyl hydroperoxide (TBHP) and tetrabutylammonium bromide (TBAB) at ambient pressure. The catalyst also shows nearly 90% selectivity for SC in reactions with styrene derivatives and retains its catalytic efficiency for up to three cycles. These results highlight IITG-7a as a promising catalyst for both the OER and CO2 conversion.
引用
收藏
页码:6214 / 6223
页数:10
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