Electrochemical synthesis of titanium nitride nanoparticles onto titanium foil for electrochemical supercapacitors with ultrafast charge/discharge

Literature Information

Publication Date 2020-03-19
DOI 10.1039/D0SE00049C
Impact Factor 6.367
Authors

Sajid Ali Ansari, Nazmul Abedin Khan, Zubair Hasan, A. A. Shaikh, Farhana K. Ferdousi, Hasi Rani Barai, Nasrin Siraj Lopa, Md. Mahbubur Rahman


View Original

Abstract

An ultrafast electrochemical supercapacitor that can deliver charge at a high rate of >1 V s−1 has great potential to supply instantaneous high power to electronic devices. Herein, a titanium nitride (TiN)-nanoparticle-modified titanium foil electrode is prepared by potentiostatic electrolysis at +5 V in an ammoniacal solution of KCl. Spectroscopic and morphological analyses reveal the formation of crystalline, homogeneous, and pure TiN nanoparticles with an average size of ∼30 nm on the Ti foil. In a three-electrode system, the optimized TiN nanoparticle-based electrode exhibits excellent rate performance and reversibility up to 3 V s−1 within the operational voltage window of 0–1.6 V. It delivers a high specific capacitance of ∼53.66 mF cm−2 at 6.66 mA cm−2 with capacity loss of only ∼3% after 10 000 charge/discharge cycles. A symmetric supercapacitor (SSC) based on the as-prepared optimized TiN nanoparticle-electrode also displays ultrafast charge/discharge characteristics with a specific capacitance of ∼44.10 mF cm−2 at 6.66 mA cm−2. This ultrafast SSC has a low relaxation time constant of ∼2.80 ms and shows excellent capacity retention (95% after 10 000 charge–discharge cycles) with ∼100% coulombic efficiency. These results demonstrate the high electrochemical stability and reversibility of TiN nanoparticles, which are promising for the development of high-performance ultrafast supercapacitors.

Related Literature

Probing the balance of attraction and repulsion in binary mixtures of dimethyl sulfoxide and n-alcohols

Andrew Ellis, Florian M. Zehentbauer

2012-11-30 Communication

DOI: 10.1039/C2CP42902K

A red-emissive aminobenzopyrano-xanthene dye: elucidation of fluorescence emission mechanisms in solution and in the aggregate state

Shinichiro Kamino, Miho Murakami, Asana Tatsumi, Noriyuki Nagaoka, Yoshinao Shirasaki, Keiko Watanabe, Kengo Yoshida, Jun Horigome, Seiji Komeda

2012-12-05 Paper

DOI: 10.1039/C2CP43503A

Symmetrisation schemes for global optimisation of atomic clusters

Mark T. Oakley, Roy L. Johnston, David J. Wales

2013-01-14 Paper

DOI: 10.1039/C3CP44332A

Back cover

Front/Back Matter

DOI: 10.1039/C2CP90028A

Clarifying the role of sodium in the silica oligomerization reaction

Anna Pavlova, Thuat T. Trinh, Rutger A. van Santen, Evert Jan Meijer

2012-11-16 Paper

DOI: 10.1039/C2CP42436C

A time-resolved spectroscopy and density functional theory study of the solvent dependent photochemistry of fenofibric acid

Ming-De Li, Jiani Ma, Tao Su, Mingyue Liu, David Lee Phillips

2012-11-16 Paper

DOI: 10.1039/C2CP41739A

Local thermal elevation probing of metal nanostructures during laser illumination utilizing surface-enhanced Raman scattering from a single-walled carbon nanotube

Shinji Hoshina, Masanobu Nara, Kei-ichiro Komeda, Ryukou Shito, Satoshi Yasuda, Kei Murakoshi

2013-02-15 Paper

DOI: 10.1039/C3CP43728K

Constrained density functional theory applied to electron tunnelling between defects in MgO

Jochen Blumberger, Keith P. McKenna

2013-01-04 Paper

DOI: 10.1039/C2CP42537H

On the inclusion of alkanes into the monolayer of aliphatic alcohols at the water/alkane vapor interface: a quantum chemical approach

Yuri B. Vysotsky, Elena S. Fomina, Elena A. Belyaeva, Valentin B. Fainerman, Dieter Vollhardt

2012-11-30 Paper

DOI: 10.1039/C2CP43713A

Dual reaction channels for photocatalytic oxidation of phenylmethanol on anatase

Ye-Fei Li, Zhi-Pan Liu

2012-11-22 Communication

DOI: 10.1039/C2CP44137C

You might also like

Compound Q&A

What industries use 4-(4-tert-Butylphenyl)-1H-pyrazol-3-amine (CAS: 1015845-73-4)?

4-(4-tert-Butylphenyl)-1H-pyrazol-3-amine finds applications in various industri...

1015845-73-44-(4-tert-Butylpheny...
Compound Q&A

What industries use H3TATAB (CAS: 63557-10-8)?

H3TATAB is used in the pharmaceutical industry for the synthesis of certain orga...

63557-10-8H3TATAB
Compound Q&A

What are the main uses of 1-Ethyl-3-fluorobenzene (CAS: 696-39-9)?

1-Ethyl-3-fluorobenzene (CAS: 696-39-9) is primarily used as a precursor in the ...

696-39-91-Ethyl-3-fluorobenz...
Compound Q&A

What are the main uses of 1-(tert-Butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid (CAS: 851484-94-1)?

1-(tert-Butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid is prim...

851484-94-11-(tert-Butoxycarbon...
Compound Q&A

What are the physical and chemical properties of 1-Cyclobutyl-4-piperidinone (CAS: 359880-05-0)?

1-Cyclobutyl-4-piperidinone (CAS: 359880-05-0) is a colorless or white crystalli...

359880-05-01-Cyclobutyl-4-piper...
Compound Q&A

What is Pyridine-2,6-dicarboxylic acid mono-tert-butyl ester (CAS: 575433-76-0)?

Pyridine-2,6-dicarboxylic acid mono-tert-butyl ester (CAS: 575433-76-0) is a che...

575433-76-0Pyridine-2,6-dicarbo...
Compound Q&A

What is the market or research trend for 2,3-Difluorophenylalanine (CAS: 236754-62-4)?

The market for 2,3-Difluorophenylalanine (CAS: 236754-62-4) is growing with incr...

236754-62-42,3-Difluorophenylal...
Compound Q&A

How is (2-Hydroxy-1-naphthyl)boronic acid (CAS: 898257-48-2) typically synthesized?

(2-Hydroxy-1-naphthyl)boronic acid can be synthesized through the reduction of 2...

898257-48-2(2-Hydroxy-1-naphthy...
1315351-28-0tert-Butyl (5-bromo-...
Compound Q&A

Are there alternatives to 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl beta-D-glucopyranoside (CAS: 19833-12-6) in synthesis?

While 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl beta-D-gluc...

19833-12-65,7-Dihydroxy-4-oxo-...
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.