Isostructural NiII Metal-Organic Frameworks (MOFs) for Efficient Electrocatalysis of Oxygen Evolution Reaction and for Gas Sorption Properties

被引:22
|
作者
Konavarapu, Satyanarayana K. [1 ]
Ghosh, Debanjali [2 ]
Dey, Avishek [1 ]
Pradhan, Debabrata [2 ]
Biradha, Kumar [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Kharagpur 721302, W Bengal, India
[2] Indian Inst Technol, Mat Sci Ctr, Kharagpur 727302, W Bengal, India
关键词
2D-layer; gas sorption; metal-organic frameworks; overpotential; oxygen evolution reaction; WATER-VAPOR; COORDINATION POLYMERS; HYDROGEN EVOLUTION; ENERGY-CONVERSION; CATALYST; NANOPARTICLES; EXPLORATION; ADSORPTION; POLYHEDRA; STORAGE;
D O I
10.1002/chem.201902274
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Design and synthesis of stable, active and cost-effective electrocatalyst for water splitting applications is an emerging area of research, given the depletion of fossil fuels. Herein, two isostructural Ni-II redox-active metal-organic frameworks (MOFs) containing flexible tripodal trispyridyl ligand (L) and linear dicarboxylates such as terephthalate (TA) and 2-aminoterphthalate (H(2)NTA) are studied for their catalytic activity in oxygen evaluation reaction (OER). The 2D-layered MOFs form 3D hydrogen bonded frameworks containing one-dimensional hydrophilic channels that are filled with water molecules. The electrochemical studies reveal that MOFs display an efficient catalytic activity towards oxygen evolution reaction in alkaline conditions with an overpotential as low as 356 mV. Further, these 2D-MOFs exhibit excellent ability to adsorb water vapor (180-230 cc g(-1) at 273 K) and CO2 (33 cc g(-1) at 273 K). The presence of hydrophilic functionality in the frameworks was found to significantly enhance the electrocatalytic activity as well as H2O sorption.
引用
收藏
页码:11141 / 11146
页数:6
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