Fe, S-uniformly dispersed Ni MOFs based on FeS substrate precipitation-dissolution equilibrium for water and seawater oxidation

Literature Information

Publication Date 2023-11-01
DOI 10.1039/D3QI01975F
Impact Factor 6.569
Authors

Na Xu, Fu-Li Wang, Jun-Qi Han, Wen-Li Yu, Wen-Jing Li, Yi-Chuan Li, Yu-Lu Zhou, Yong-Ming Chai, Bin Dong


View Original

Abstract

In the pursuit of advancing electrocatalysts for the alkaline oxygen evolution reaction (OER), the development of nickel-based metal–organic frameworks (MOFs) with a judicious balance of cost-effectiveness and catalytic efficacy is of paramount importance. Herein, we have achieved a commendable feat in the synthesis of Ni MOFs integrated with uniformly dispersed Fe and S species on a FeS substrate based on the precipitation-dissolution equilibrium. For the obtained Ni MOFs/FeS/IF catalyst, three factors including excellent conductivity of FeS substrate, conjugated carboxylate ligands and spindle-shaped structure with uniformly dispersed Fe and S can contribute to the enhanced activity for OER. The electrochemical measurements show that Ni MOFs/FeS/IF requires overpotentials of 250 and 280 mV to reach current densities of 100 mA cm−2 in 1 M KOH and 1 M KOH seawater, respectively, as compared to that (427@100 mA cm−2 in 1 M KOH, 455@100 mA cm−2 in 1 M KOH seawater) of Ni MOFs/NF. Interestingly, the Ni MOFs/FeS/IF electrode displayed remarkable electrochemical stability with a high current density of 500 mA cm−2 after testing for 50 h, which is attributed to the synergistic effect of the bimetallic centers and optimized coordination environments via Ni–S bonds. The study reveals the potential for efficiently driving freshwater and seawater splitting by uniformly distributing anions and cations based on the precipitation-dissolution equilibrium during the in situ generation of metal–organic frameworks toward advanced electrocatalysts.

Related Literature

Courses

Other

DOI: 10.1039/AN995200038N

Courses

Other

DOI: 10.1039/AN996210176N

Recent IUPAC recommendations

Other

DOI: 10.1039/AN995200151N

Back matter

Other

DOI: 10.1039/AN99621BP007

Front cover

Other

DOI: 10.1039/AN99621FX054

Contents pages

Other

DOI: 10.1039/AN99520BX039

Papers in future issues

Other

DOI: 10.1039/AN995200071N

You might also like

Compound Q&A

What precautions should be taken when handling lithium chloride hydrate (1:1:1) (CAS: 16712-20-2)?

When handling lithium chloride hydrate (1:1:1) (CAS: 16712-20-2), it is importan...

16712-20-2Lithium chloride hyd...
Compound Q&A

Is 4-(4H-1,2,4-Triazol-4-yl)piperidine (CAS: 690261-92-8) safe?

4-(4H-1,2,4-Triazol-4-yl)piperidine is generally considered safe for use in phar...

690261-92-84-(4H-1,2,4-Triazol-...
Compound Q&A

How should waste containing 1,3-Thiazole-2-carboxamide (CAS: 16733-85-0) be handled?

Waste containing 1,3-Thiazole-2-carboxamide (CAS: 16733-85-0) should be collecte...

16733-85-01,3-Thiazole-2-carbo...
Compound Q&A

What regulatory guidelines apply to 5-(Difluoromethyl)-2-fluorobenzonitrile (CAS: 934175-58-3)?

5-(Difluoromethyl)-2-fluorobenzonitrile (CAS: 934175-58-3) is subject to regulat...

934175-58-35-(Difluoromethyl)-2...
Compound Q&A

How is Methyl 3-acetamido-2-thiophenecarboxylate (CAS: 22288-79-5) typically synthesized?

Methyl 3-acetamido-2-thiophenecarboxylate can be synthesized by the reaction of ...

22288-79-5Methyl 3-acetamido-2...
Compound Q&A

What is 4-Isoquinolinecarbonitrile (CAS: 34846-65-6)?

4-Isoquinolinecarbonitrile is a chemical compound with the CAS number 34846-65-6...

34846-65-64-Isoquinolinecarbon...
Compound Q&A

How should Methyl 1H-1,2,3-triazole-4-carboxylate (CAS: 877309-59-6) be stored?

Store Methyl 1H-1,2,3-triazole-4-carboxylate (CAS: 877309-59-6) in a cool, dry p...

877309-59-6Methyl 1H-1,2,3-tria...
Compound Q&A

What regulatory guidelines apply to 6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine (CAS: 1160791-13-8)?

6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine (CAS: 1160791-13-8) is subject to the...

1160791-13-86-Bromo[1,3]thiazolo...
Compound Q&A

Is (2S,3S)-2-Ammonio-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoate (CAS: 23651-95-8) safe?

(2S,3S)-2-Ammonio-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoate (CAS: 23651-95-8) ...

23651-95-8(2S,3S)-2-Ammonio-3-...
Compound Q&A

What are the physical and chemical properties of 7-bromo-3-methyl-3,4-dihydroquinazolin-4-one (CAS: 1293987-84-4)?

7-Bromo-3-methyl-3,4-dihydroquinazolin-4-one is a solid with a crystalline form....

1293987-84-47-bromo-3-methyl-3,4...

Source Journal

Inorganic Chemistry Frontiers

Inorganic Chemistry Frontiers
CiteScore: 10.4
Self-citation Rate: 6.6%
Articles per Year: 625

Inorganic Chemistry Frontiers publishes research articles, reviews, notes, comments and methods covering all areas of inorganic chemistry. Emphases are placed on interdisciplinary studies where inorganic chemistry and organometallic chemistry meet related areas, such as catalysis, biochemistry, nanoscience, energy and materials science. For publication in Inorganic Chemistry Frontiers, papers should report high-quality work of exceptional novelty, which will be of significant interest to the wide readership of the journal.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.