Cu3P/PAN derived N-doped carbon catalyst with non-toxic synthesis for alkaline hydrogen evolution reaction

Literature Information

Publication Date 2020-08-26
DOI 10.1039/D0SE00923G
Impact Factor 6.367
Authors

HyoWon Kim, Yongju Lee, DongHoon Song, YongKeun Kwon, Eom-Ji Kim, EunAe Cho


View Original

Abstract

To utilize hydrogen as an energy carrier to store surplus electricity, it is necessary to develop a highly efficient and low-cost hydrogen evolution reaction (HER) catalyst for water electrolysis. This work presents an alkaline HER catalyst composed of earth-abundant elements. Through a one-step facile and non-toxic process that combines the phosphorization of copper and the cyclization of polyacrylonitrile (PAN), copper phosphide (Cu3P) particles embedded in nitrogen-doped carbon were synthesized (Cu3P/N–C). In the complex structure, Cu3P is catalytically active towards the HER and N-doped carbon connects the Cu3P particles electrically and physically. Thus, the incorporation of N-doped carbon simply by adding PAN to a phosphorus precursor improves the electrical conductivity and structural integrity of the Cu3P electrode during the HER. To achieve the best HER activity, the P-to-PAN ratio was optimized. Cu3P/N–C prepared on copper foam showed HER overpotentials of 211.1 and 301.8 mV to obtain corresponding current density of 10 and 50 mA cm−2 in a 1 M KOH solution. At the current density of 10 mA cm−2, the HER overpotential was stably maintained from 211.1 to 222.1 mV for 24 h. In addition to the enlarged electrochemical active surface area (ECSA), the synergistic effects of the disordered carbon structure formed by the influence of the P source result in the superior performance outcomes of Cu3P/N–C.

Related Literature

Tunable mosaic structures in van der Waals layered materials

Silong Quan, Linghui He, Yong Ni

2018-09-10 Paper

DOI: 10.1039/C8CP04360D

Ferroelectric-mediated filamentary resistive switching in P(VDF-TrFE)/ZnO nanocomposite films

Tae Yeon Kim, Gopinathan Anoop, Yeong Jun Son, Soo Hyeon Kim, Eunji Lee, Ji Young Jo

2018-04-30 Paper

DOI: 10.1039/C8CP02024H

Inside back cover

Cover

DOI: 10.1039/C8CP91861A

Constructing organic superacids from superhalogens is a rational route as verified by DFT calculations

Fu-Qiang Zhou, Ru-Fang Zhao, Jin-Feng Li, Wen-Hua Xu, Chao-Chao Li, Lan Luo, Jian-Li Li, Bing Yin

2019-01-04 Paper

DOI: 10.1039/C8CP07313A

The evaporation kinetics of pure water droplets at varying drying rates and the use of evaporation rates to infer the gas phase relative humidity

Yong-yang Su, Rachael E. H. Miles, Zhi-ming Li, Jonathan P. Reid, Jiang Xu

2018-08-31 Paper

DOI: 10.1039/C8CP05250F

Correction: Surface induced smectic order in ionic liquids – an X-ray reflectivity study of [C22C1im]+[NTf2]−

Henning Weiss, Hailong Li, Oleg Konovalov, Sven Festersen, Uta Rütt

2018-09-12 Correction

DOI: 10.1039/C8CP91851A

Stability of metallo-porphyrin networks under oxygen reduction and evolution conditions in alkaline media

Diana Hötger, Markus Etzkorn, Benjamin Wurster, Jan Dreiser, Sebastian Stepanow, Doris Grumelli, Rico Gutzler

2019-01-11 Paper

DOI: 10.1039/C8CP07463A

Anchoring of carboxyl-functionalized porphyrins on MgO, TiO2, and Co3O4 nanoparticles

Fabian Kollhoff, Johannes Schneider, Gao Li, Sami Barkaoui, Wenjie Shen, Thomas Berger, Oliver Diwald

2018-09-11 Paper

DOI: 10.1039/C8CP04873H

Reversible DNA compaction induced by partial intercalation of 16-Ph-16 gemini surfactants: evidence of triple helix formation

Elia Grueso, Emilio Roldan, Pilar Perez-Tejeda, Edyta Kuliszewska, Blanca Molero, Lothar Brecker, R. M. Giráldez-Pérez

2018-09-14 Paper

DOI: 10.1039/C8CP02791A

You might also like

Compound Q&A

Is 2-(2-chloroacetamido)-3-phenylpropanoic acid (CAS: 7765-11-9) safe?

2-(2-Chloroacetamido)-3-phenylpropanoic acid (CAS: 7765-11-9) is generally consi...

7765-11-92-(2-chloroacetamido...
Compound Q&A

Is 2-(Benzyloxy)-5-bromobenzoic acid (CAS: 62176-31-2) safe?

2-(Benzyloxy)-5-bromobenzoic acid can be handled safely if appropriate precautio...

62176-31-22-(Benzyloxy)-5-brom...
Compound Q&A

What is (4-Methyl-1,2,5-oxadiazol-3-yl)methanamine hydrochloride (CAS: 1159825-48-5)?

(4-Methyl-1,2,5-oxadiazol-3-yl)methanamine hydrochloride is a chemical compound ...

1159825-48-5(4-Methyl-1,2,5-oxad...
Compound Q&A

What is 2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 917985-54-7)?

2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 917985-54...

917985-54-72-(5-Hexylthiophen-2...
Compound Q&A

Are there alternatives to 4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine (CAS: 102771-26-6) in synthesis?

While 4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine (CAS:...

102771-26-64-(8-Methyl-9H-1,3-d...
Compound Q&A

What is the market or research trend for tert-butyl 3-hydroxy-4,5,7,8-tetrahydro-2H-pyrazolo[3,4-d]azepine-6-carboxylate (CAS: 851376-80-2)?

The market for tert-butyl 3-hydroxy-4,5,7,8-tetrahydro-2H-pyrazolo[3,4-d]azepine...

851376-80-2tert-butyl 3-hydroxy...
Compound Q&A

How should waste containing 3,5-Diamino-1H-pyrazole-4-carbonitrile (CAS: 6844-58-2) be handled?

Waste containing 3,5-Diamino-1H-pyrazole-4-carbonitrile (CAS: 6844-58-2) should ...

6844-58-23,5-Diamino-1H-pyraz...
Compound Q&A

How is (6-Fluoro-3-pyridinyl)boronic acid (CAS: 351019-18-6) typically synthesized?

(6-Fluoro-3-pyridinyl)boronic acid can be synthesized through the reaction of 6-...

351019-18-6(6-Fluoro-3-pyridiny...
Compound Q&A

What industries use Dibenzyl carbonimidoylbiscarbamate (CAS: 10065-79-9)?

Dibenzyl carbonimidoylbiscarbamate (CAS: 10065-79-9) finds applications in vario...

10065-79-9Dibenzyl carbonimido...
Compound Q&A

What is the market or research trend for (beta,beta,2,3,4,5,6-~2~H_7_)Phenylalanine (CAS: 74228-83-4)?

The market for (beta,beta,2,3,4,5,6-~2~H_7_)Phenylalanine (CAS: 74228-83-4) is g...

74228-83-4(beta,beta,2,3,4,5,6...
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.