Co–Mo–P carbon nanospheres derived from metal–organic frameworks as a high-performance electrocatalyst towards efficient water splitting

2021 ◽  
Author(s):  
Nan Li ◽  
Yi Guan ◽  
Yongliang Li ◽  
Hongwei Mi ◽  
Libo Deng ◽  
...  
Keyword(s):  
Free Energy ◽  
Electron Transport ◽  
Water Splitting ◽  
Active Site ◽  
Electrocatalytic Activity ◽  
High Performance ◽  
Metal Organic Frameworks ◽  
Carbon Nanospheres ◽  
Metal Organic

A well-designed Co–Mo–P active site allows electron transport between Co and MoP, which will reduce the absorption free energy of the intermediates and improve the electrocatalytic activity of the hybrid.

scholarly journals Correction: Co–Mo–P carbon nanospheres derived from metal–organic frameworks as a high-performance electrocatalyst towards efficient water splitting

2021 ◽  
Author(s):  
Nan Li ◽  
Yi Guan ◽  
Yongliang Li ◽  
Hongwei Mi ◽  
Libo Deng ◽  
...  
Keyword(s):  
Water Splitting ◽  
High Performance ◽  
Metal Organic Frameworks ◽  
Carbon Nanospheres ◽  
Metal Organic

Correction for ‘Co–Mo–P carbon nanospheres derived from metal–organic frameworks as a high-performance electrocatalyst towards efficient water splitting’ by Nan Li et al., J. Mater. Chem. A, 2021, 9, 1143–1149, DOI: 10.1039/D0TA10426D.

High-Performance Overall Water Splitting Electrocatalysts Derived from Cobalt-Based Metal–Organic Frameworks

2015 ◽  
Vol 27 (22) ◽  
pp. 7636-7642 ◽  
Author(s):  
Bo You ◽  
Nan Jiang ◽  
Meili Sheng ◽  
Sheraz Gul ◽  
Junko Yano ◽  
...  
Keyword(s):  
Water Splitting ◽  
High Performance ◽  
Metal Organic Frameworks ◽  
Overall Water Splitting ◽  
Metal Organic

Rational strategies for proton-conductive metal–organic frameworks

2021 ◽  
Author(s):  
Dae-Woon Lim ◽  
Hiroshi Kitagawa
Keyword(s):  
Solid State ◽  
Potential Application ◽  
High Performance ◽  
Metal Organic Frameworks ◽  
Metal Organic ◽  
Solid State Electrolytes

Since the transition of energy platforms, the proton-conductive metal–organic frameworks (MOFs) exhibiting high performance have been extensively investigated with rational strategies for their potential application in solid-state electrolytes.

Protein Immobilization in Metal–Organic Frameworks by Covalent Binding

2014 ◽  
Vol 67 (11) ◽  
pp. 1629 ◽  
Author(s):  
Xuan Wang ◽  
Trevor A. Makal ◽  
Hong-Cai Zhou
Keyword(s):  
Enzymatic Activity ◽  
Enzyme Immobilization ◽  
Working Conditions ◽  
Active Site ◽  
Covalent Binding ◽  
Metal Organic Frameworks ◽  
Protein Immobilization ◽  
Immobilization Of Enzymes ◽  
Metal Organic ◽  
Biological Catalysis

Metal–organic frameworks (MOFs), possessing a well defined system of pores, demonstrate extensive potential serving as a platform in biological catalysis. Successful immobilization of enzymes in a MOF system retains the enzymatic activity, renders the active site more accessible to the substrate, and promises recyclability for reuse, and solvent adaptability in a broad range of working conditions. This highlight describes enzyme immobilization on MOFs via covalent binding and its significance.

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