Designing bifunctional catalysts for urea electrolysis: progress and perspectives

Literature Information

Publication Date 2023-12-04
DOI 10.1039/D3GC03329E
Impact Factor 10.182
Authors

Zhijie Chen, Wei Wei, Ho Kyong Shon


View Original

Abstract

Recently, urea electrolysis has become an attractive method for sustainable energy-saving hydrogen production and simultaneous pollutant degradation. To improve urea electrolysis efficiency and simplify electrolysis systems, developing efficient bifunctional electrocatalysts has attracted great interest. Recently, great achievements have been made in the design of high-performance bifunctional catalysts for urea electrolysis. In this review, the current progress in bifunctional catalysts for urea electrolysis is comprehensively analyzed. The fundamentals and catalyst design principles for urea electrolysis are first discussed. Then, the applications of advanced bifunctional catalysts in urea electrolysis are fully demonstrated, such as single atom catalysts (SACs), metal nanoparticles, alloys, metal (hydr)oxides, chalcogenides, pnictides, metal–organic frameworks (MOFs), and composites. The structure–performance correlation of catalysts as well as their design strategies are emphasized. Current catalysts are also evaluated in terms of their catalytic activities, providing insights into the sensible design of high-performance bifunctional electrocatalysts. Several key perspectives are outlined to guide further studies on practical urea electrolysis-driven sustainable hydrogen production and urea-rich wastewater management.

Related Literature

Insights into the mechanism of electrochemical ozone production via water splitting on the Ni and Sb doped SnO2 catalyst

Ziyun Wang, Christopher Hardacre, Wen-Feng Lin

2017-01-11 Paper

DOI: 10.1039/C6CP06906A

Temperature-dependent ESR and computational studies on antiferromagnetic electron transfer in the yeast NADH dehydrogenase Ndi1

Kaiqi Wu, Wenfei Li, Lu Yu, Wei Tong, Yue Feng, Shenglong Ling, Longhua Zhang, Xiao Zheng, Maojun Yang

2017-01-09 Paper

DOI: 10.1039/C6CP08107J

Charge transport in organic donor–acceptor mixed-stack crystals: the role of nonlocal electron–phonon couplings

Lingyun Zhu, Hua Geng, Yuanping Yi, Zhixiang Wei

2017-01-06 Paper

DOI: 10.1039/C6CP07417K

Suitability of N-propanoic acid spiropyrans and spirooxazines for use as sensitizing dyes in dye-sensitized solar cells

Noah M. Johnson, Yuriy Y. Smolin, Daniel Hagaman, Masoud Soroush, Kenneth K. S. Lau, Hai-Feng Ji

2017-01-04 Paper

DOI: 10.1039/C6CP07853B

Triplet exciton dissociation and electron extraction in graphene-templated pentacene observed with ultrafast spectroscopy

Thomas J. McDonough, Lushuai Zhang, Susmit Singha Roy, Nicholas M. Kearns, Michael S. Arnold, Martin T. Zanni

2017-01-23 Paper

DOI: 10.1039/C6CP06454J

Contents list

Front/Back Matter

DOI: 10.1039/C7CP90024D

Fast and accurate MAS–DNP simulations of large spin ensembles

Shimon Vega

2017-01-05 Paper

DOI: 10.1039/C6CP07881H

Front cover

Cover

DOI: 10.1039/C7CP90016C

Molecular aggregation of naphthalimide organic semiconductors assisted by amphiphilic and lipophilic interactions: a joint theoretical and experimental study

I. Arrechea-Marcos, M. J. Mancheño, M. C. Ruiz Delgado, M. M. Ramos, J. A. Quintana, J. M. Villalvilla, M. A. Díaz-García, J. T. López Navarrete, R. Ponce Ortiz, J. L. Segura

2017-02-03 Paper

DOI: 10.1039/C6CP06819G

You might also like

Compound Q&A

What precautions should be taken when handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3)?

When handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3), it ...

79206-94-34-(2-Furylmethyl)thi...
Compound Q&A

What precautions should be taken when handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9)?

When handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9), it...

71320-77-94-Chloro-N-[2-(4-mor...
Compound Q&A

How should waste containing 2-[2-(2-Methoxyethoxy)ethoxy]ethyl 4-methylbenzenesulfonate (CAS: 62921-74-8) be handled?

Waste containing this compound (CAS: 62921-74-8) should be handled according to ...

62921-74-82-[2-(2-Methoxyethox...
Compound Q&A

How should waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate be handled?

Waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate should be collected i...

40056-18-6(S)-Methyl 2-amino-3...
166882-70-85-({4-[(2S,4R)-4-Hyd...
Compound Q&A

Are there alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid (CAS: 7312-27-8) in synthesis?

There are several alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid in syn...

7312-27-8(2E)-3-(3,4-Dichloro...
Compound Q&A

How should Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84-9) be stored?

Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84...

925437-84-9Ethyl 6-(2-nitrophen...
Compound Q&A

How should waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) be handled?

Waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) should be coll...

18453-07-12-(1,3-Thiazol-2-yl)...
Compound Q&A

How is Methyl 5-iodo-2-methylbenzoate (CAS: 103440-54-6) typically synthesized?

Methyl 5-iodo-2-methylbenzoate can be synthesized through the iodination of meth...

103440-54-6Methyl 5-iodo-2-meth...
Compound Q&A

How is 5-Chloro[1,2,4]triazolo[1,5-a]pyridine (CAS: 1427399-34-5) typically synthesized?

5-Chloro[1,2,4]triazolo[1,5-a]pyridine is commonly synthesized via the condensat...

1427399-34-55-Chloro[1,2,4]triaz...

Source Journal

Green Chemistry

Green Chemistry
CiteScore: 16.1
Self-citation Rate: 7.5%
Articles per Year: 944

Green Chemistry provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on, but not limited to, the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998). Green chemistry is the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry is at the frontiers of this continuously-evolving interdisciplinary science and publishes research that attempts to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. Submissions on all aspects of research relating to the endeavour are welcome. The journal publishes original and significant cutting-edge research that is likely to be of wide general appeal. To be published, work must present a significant advance in green chemistry. Papers must contain a comparison with existing methods and demonstrate advantages over those methods before publication can be considered. For more information please see this Editorial. Coverage includes the following, but is not limited to: Design (e.g. biomimicry, design for degradation/recycling/reduced toxicity…) Reagents & Feedstocks (e.g. renewables, CO2, solvents, auxiliary agents, waste utilization…) Synthesis (e.g. organic, inorganic, synthetic biology…) Catalysis (e.g. homogeneous, heterogeneous, enzyme, whole cell…) Process (e.g. process design, intensification, separations, recycling, efficiency…) Energy (e.g. renewable energy, fuels, photovoltaics, fuel cells, energy storage, energy carriers…) Applications (e.g. electronics, dyes, consumer products, coatings, pharmaceuticals, preservatives, building materials, chemicals for industry/agriculture/mining…) Impact (e.g. safety, metrics, LCA, sustainability, (eco)toxicology…) Green chemistry is, by definition, a continuously-evolving frontier. Therefore, the inclusion of a particular material or technology does not, of itself, guarantee that a paper is suitable for the journal. To be suitable, the novel advance should have the potential for reduced environmental impact relative to the state of the art. Green Chemistry does not normally deal with research associated with 'end-of-pipe' or remediation issues.

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.