Hydrophilic “bridge” H–C3N4 stabilizing CuO onto graphenes with enhanced energy density for asymmetric supercapacitors

Literature Information

Publication Date 2020-06-02
DOI 10.1039/D0SE00414F
Impact Factor 6.367
Authors

Yue Li, Pascal Kamdem, Chen Cheng, Xiao-Juan Jin, Xinyan Liu


View Original

Abstract

Electroactive species grafted onto graphenes hold great potential as electrode composites for distinguished property supercapacitors. However, the weak bonding and incompatibility between inorganic electroactive species and reduced graphene oxide (rGO) substrates still need to be settled. In this work, H–C3N4 as a novel hydrophilic “bridge” to stabilize CuO anchoring on a graphene substrate was designed to fabricate hydrophilic hybrids. The CuO/H–C3N4/rGO hybrid features a hydrophilic nitrogen-containing functional group, which could exhibit high conductivity and possesses numerous electroactive sites, facilitating fast transfer between electrons and electrolyte ions. In addition, H–C3N4 as a hydrophilic “nano-bridge” could moderate the electronic structural states and firmly combine CuO, the catalytic center, with the substrate rGO, which could enhance the stability of the CuO/H–C3N4/rGO hybrid. Benefiting from these, the as-fabricated CuO/H–C3N4/rGO electrode could exhibit outstanding electrochemical properties with a specific capacitance of 816 F g−1 at a current density of 0.5 A g−1 and 639 F g−1 even at a high current density of 20 A g−1. In addition, the specific capacitance of the CuO/H–C3N4/rGO electrode could maintain 84.38% of the original value after 10 000 cycles. Besides, the asymmetric supercapacitors with the CuO/H–C3N4/rGO hybrid as the anode and activated carbon as the cathode could exhibit a high energy density of 73.85 W h kg−1 at a power density of 0.493 kW kg−1. Moreover, H–C3N4 as “glue” could be used to fabricate certain kinds of active species on different substrates and hold the potential for preparing efficient and robust electrode hybrids for application in various fields.

Related Literature

A facile tandem decyanation/cyanation reaction of α-iminonitriles toward cyano-substituted amides

Pei Liang, Botao Liu, Haiqing Luo, Jing Zheng, Xiaowei Wen, Tanggao Liu, Min Ye

2018-10-25 Communication

DOI: 10.1039/C8OB02186D

Investigations into the mechanism of action of nitrobenzene as a mild dehydrogenating agent under acid-catalysed conditions

M. Lurdes S. Cristiano, David J. P. Gago, Antonio M. d'A. Rocha Gonsalves, Robert A. W. Johnstone, Moya McCarron

2003-01-20 Paper

DOI: 10.1039/B210887A

A cascade synthesis of S-allyl benzoylcarbamothioates via Mumm-type rearrangement

Anjali Dahiya, Wajid Ali, Tipu Alam, Bhisma K. Patel

2018-10-09 Communication

DOI: 10.1039/C8OB02293C

Bimodal fluorogenic sensing of matrix proteolytic signatures in lung cancer

Alicia Megia-Fernandez, Bethany Mills, Chesney Michels, Sunay V. Chankeshwara, Nikola Krstajić, Chris Haslett, Kevin Dhaliwal, Mark Bradley

2018-08-23 Paper

DOI: 10.1039/C8OB01790E

Differential substituent effects of β-halogens in water-soluble porphyrins

Justin C. Biffinger, Haoran Sun, Andrew P. Nelson, Stephen G. DiMagno

2003-01-24 Paper

DOI: 10.1039/B209345F

Synthesis, absolute configuration and conformation of optically active 1,2-homoheptafulvalene

Shunji Ito, Mitsuhiro Kurita, Sigeru Kikuchi, Toyonobu Asao, Yoshitora Ito, Masaji Oda, Hideo Sotokawa, Akio Tajiri, Noboru Morita

2003-01-15 Paper

DOI: 10.1039/B210949M

Immune responses against Lewis Y tumor-associated carbohydrate antigen displayed densely on self-assembling nanocarriers

Yuji Yamazaki, Yukiko Nambu, Masashi Ohmae, Manabu Sugai, Shunsaku Kimura

2018-10-03 Paper

DOI: 10.1039/C8OB01955J

Tuning the keto equilibrium in 4-substituted dipicolinic acid derivatives

Anne-Sophie Chauvin, Sandrine Gras, Jean-Claude G. Bünzli

2003-01-22 Paper

DOI: 10.1039/B211267C

Tetracyclic pyrazine-fused furazans as insensitive energetic materials: syntheses, structures, and properties

Qi Sun, Xin Li, Qiuhan Lin, Ming Lu

2018-10-11 Communication

DOI: 10.1039/C8OB02155D

The base-catalysed cyclisation of phenyl N-(2-hydroxybenzyl)-N-methylcarbamates is concerted

Vojeslav Štěrba, Oldřich Hrabík, Jaromír Kaválek, Jaromír Mindl, Andrew Williams

2002-12-11 Paper

DOI: 10.1039/B209323P

You might also like

Compound Q&A

Is 4-Benzyl-2,2-dimethylmorpholine (CAS: 84761-04-6) safe?

4-Benzyl-2,2-dimethylmorpholine is generally considered safe when handled under ...

84761-04-64-Benzyl-2,2-dimethy...
Compound Q&A

What is (5,6-Dimethoxy-3-pyridinyl)boronic acid (CAS: 1346526-61-1)?

(5,6-Dimethoxy-3-pyridinyl)boronic acid is a chemical compound with the molecula...

1346526-61-1(5,6-Dimethoxy-3-pyr...
Compound Q&A

How is 1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane (CAS: 67875-55-2) typically synthesized?

1,1,3,3-Tetramethyl-1,3-bis(2-methyl-2-propanyl)disiloxane is synthesized throug...

67875-55-21,1,3,3-Tetramethyl-...
Compound Q&A

What are the main uses of (2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid (CAS: 1018818-04-6)?

(2R,4S)-1-Boc-4-methylpyrrolidine-2-carboxylic acid is primarily used as a build...

1018818-04-6(2R,4S)-1-Boc-4-meth...
Compound Q&A

What precautions should be taken when handling 2,3-Dichloroacrylonitrile (CAS: 22410-58-8)?

When handling 2,3-Dichloroacrylonitrile, it is crucial to wear appropriate perso...

22410-58-82,3-Dichloroacryloni...
Compound Q&A

How should (S)-1-(o-Tolyl)ethanamine hydrochloride (CAS: 1332832-16-2) be stored?

(S)-1-(o-Tolyl)ethanamine hydrochloride should be stored in a cool, dry place to...

1332832-16-2(S)-1-(o-Tolyl)ethan...
Compound Q&A

What are the physical and chemical properties of Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8)?

Benzyl [1-(hydroxyamino)-1-imino-2-methyl-2-propanyl]carbamate (CAS: 518047-98-8...

518047-98-8Benzyl [1-(hydroxyam...
Compound Q&A

What industries use 2-Methyloxazole-5-carbaldehyde (CAS: 885273-42-7)?

2-Methyloxazole-5-carbaldehyde is used in the pharmaceutical industry for the sy...

885273-42-72-Methyloxazole-5-ca...
Compound Q&A

What is the market or research trend for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxylate (CAS: 389889-82-1)?

The market for 2-Methyl-2-propanyl 4-[(1S)-1-hydroxyethyl]-1-piperidinecarboxyla...

389889-82-12-Methyl-2-propanyl ...
Compound Q&A

Is 1-Butyl-3-methylpyridinium bromide (CAS: 26576-85-2) safe?

1-Butyl-3-methylpyridinium bromide is generally considered safe for laboratory u...

26576-85-21-Butyl-3-methylpyri...

Source Journal

Sustainable Energy & Fuels

Sustainable Energy & Fuels
CiteScore: 0
Self-citation Rate: 0%
Articles per Year: 0

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.