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A noble metal-free candle soot derived carbon electrocatalyst for simultaneous H2 generation and wastewater treatment
被引:3
|作者:
Pahra, Swapna
[1
,2
]
Sangabathula, Omkar
[3
]
Sharma, Chandra S.
[3
]
Devi, Pooja
[1
]
机构:
[1] CSIR Cent Sci Instruments Org, Mat Sci & Sensor Applicat, Chandigarh 160030, India
[2] Acad Sci & Innovat Res, Ghaziabad 201002, India
[3] Indian Inst Technol Hyderabad, Dept Chem Engn, Creat & Adv Res Based Nanomat CARBON Lab, Kandi 502285, Telangana, India
关键词:
Water treatment;
Carbon soot derived carbon;
Hydrogen evolution reaction;
Electrocatalyst;
Waste water treatment;
EFFICIENT BIFUNCTIONAL ELECTROCATALYSTS;
OXYGEN EVOLUTION REACTION;
HYDROGEN EVOLUTION;
HIGHLY EFFICIENT;
STAINLESS-STEEL;
METHYLENE-BLUE;
SURFACE-AREA;
NICKEL FOAM;
ELECTRODE;
GRAPHENE;
D O I:
10.1016/j.jpcs.2022.111106
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Electrocatalytic water splitting to produce green hydrogen is a promising approach for clean energy generation. However, the commercial aspect of this approach is limited due to catalysts cost and feedstock. Thus design of an inexpensive and noble metal-free (Pt, Rh, Ir etc.) catalyst is desirable. Moreover, wastewater as a feedstock for hydrogen generation is not explored to its full potential for green hydrogen generation, which otherwise is also a problem to be managed especially in developing countries. In the present work, we have investigated an inex-pensive catalyst i.e. candle soot-derived carbon as an electrocatalyst for H2 generation from textile wastewater utilizing methylene blue as a model pollutant. The carbon catalyst is synthesized from the candle soot and is characterized for its structural and morphological properties. Carbon soot coated onto the nickel foam (CS@NF) proves as an efficient hydrogen evolution catalyst due to its excellent electrical conductivity and large active surface area. CS2.5@NF (with the loading of 2.5 mg cm-2) shows an overpotential and Tafel slope of 117 mV and 43.85 mV/dec, respectively in an acidic medium containing textile pollutants. Under optimal condition,-62% degradation is achieved within-90 min, along with the stable hydrogen production of-0.158 mmol per hour. These preliminary findings demonstrate the potential usage of an inexpensive non-noble metal free catalyst for simultaneous wastewater treatment as well as hydrogen generation.
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