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Microwave-Assisted Fabrication of Copper Oxide/N-Doped Carbon Nanocatalyst for Efficient Electrochemical CO2 Conversion to Liquid Fuels
被引:0
|作者:
Banerjee, Anwesha
[1
]
Jain, Siddarth
[1
]
Dastider, Saptarshi Ghosh
[2
,3
]
Biswas, Rathindranath
[1
]
Das, Srewashi
[1
]
Mondal, Krishnakanta
[3
]
Vishal, Vikram
[4
,5
,6
]
Lahiri, Goutam Kumar
[1
]
Dutta, Arnab
[1
,5
,6
]
机构:
[1] Indian Inst Technol, Chem Dept, Powai 400076, Maharashtra, India
[2] Cent Univ Punjab, Dept Chem, Bathinda 151401, Punjab, India
[3] Univ Delhi, Dept Phys & Astrophys, New Delhi 110007, India
[4] Indian Inst Technol, Earth Sci Dept, Powai 400076, Maharashtra, India
[5] Indian Inst Technol, Natl Ctr Excellence Carbon Capture & Utilizat NCoE, Powai 400076, Maharashtra, India
[6] Indian Inst Technol, Interdisciplinary Program Climate Studies, Powai 400076, Maharashtra, India
来源:
关键词:
CO2;
electrolyzer;
reduction;
carbon capture and utilization;
copper oxide;
flue gas;
formate;
methanol;
microwave-assisted pathway;
REDUCTION;
ELECTROREDUCTION;
DIOXIDE;
NANOPARTICLES;
STABILITY;
METHANOL;
D O I:
10.1002/smll.202406765
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Electrochemical CO2 reduction reaction (CO2RR), which is driven by electricity generated from renewable energy sources, is a promising technology for sustainably producing carbon-based chemicals or fuels. Several CO2RR catalysts have been explored to date, among which copper-based electrocatalysts are the most widely known for electrochemical CO2RR and are extensively studied for their ability to generate an array of products. Their low selectivity, however, hinders their possibility of being used for practical purposes. In this work, a microwave-assisted one-pot synthesized CuxO/N-doped carbon demonstrates the electrochemical conversion of carbon dioxide into multiple C-1 products (mainly formate and methanol), with a maximum Faradaic efficiency of 95% in 0.10 m KHCO3 aqueous solution at a moderately low applied potential of -0.55 V versus RHE (reversible hydrogen electrode). The in-depth theoretical study reveals the key contribution of pyridinic N-based N-doped carbon sites and Cu2O clusters in CO2 adsorption and its subsequent conversion to formate and methanol via an energetically favorable formate pathway. The electrocatalyst continued to demonstrate CO2 reduction to valuable C-1 products when a simulated flue gas stream containing 15% CO2 along with 500 ppm SOx and 200 ppm NOx is used as an inlet feed.
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