Carbon-Based Electrodes and Catalysts for the Electroreduction of Carbon Dioxide (CO2) to Value-Added Chemicals

Author(s):  
Sumit Verma ◽  
Uzoma O. Nwabara ◽  
Paul J. A. Kenis
Author(s):  
Rajasekaran Elakkiya ◽  
Govindhan Maduraiveeran

Design of high-performance and Earth-abundant electrocatalysts for electrochemical carbon dioxide (CO2) reduction reaction (CO2RR) into fuels and value-added chemicals offers an emergent pathway for environment and energy sustainable concerns. Herein,...


Author(s):  
Zhuang-Zhuang Niu ◽  
Li-Ping Chi ◽  
Ren Liu ◽  
Zhi Chen ◽  
Min-Rui Gao

Electrochemical conversion of carbon dioxide (CO2) into valuable carbon-based chemicals provides a route to store renewable electricity and close the carbon loop. In comparison to the conventional "H-cells", the flow-cell...


Author(s):  
Chuqian Xiao ◽  
Ling Cheng ◽  
Yating Wang ◽  
Jinze Liu ◽  
Rongzhen Chen ◽  
...  

Anodic selective electro‐oxidation of methanol paring with cathodic carbon dioxide (CO2) reduction is regarded as a promising strategy to generate value added formate product. We firstly design a 3D‐assembled NiCo...


Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 413 ◽  
Author(s):  
Silvia Mena ◽  
Iluminada Gallardo ◽  
Gonzalo Guirado

Carbon dioxide (CO2) is a known greenhouse gas, and is the most important contributor to global warming. Therefore, one of the main challenges is to either eliminate or reuse it through the synthesis of value-added products, such as carboxylated derivatives. One of the most promising approaches for activating, capturing, and valorizing CO2 is the use of electrochemical techniques. In the current manuscript, we described an electrocarboxylation route for synthesizing 4-cyanobenzoic acid by valorizing CO2 through the synergistic use of electrochemical techniques (“green technology”) and ionic liquids (ILs) (“green solvents”)—two of the major entries in the general green chemistry tool kit. Moreover, the use of silver cathodes and ILs enabled the electrochemical potential applied to be reduced by more than 0.4 V. The “green” synthesis of those derivatives would provide a suitable environmentally friendly process for the design of plasticizers based on phthalate derivatives.


2018 ◽  
Vol 31 (13) ◽  
pp. 1804257 ◽  
Author(s):  
Jingjie Wu ◽  
Tiva Sharifi ◽  
Ying Gao ◽  
Tianyu Zhang ◽  
Pulickel M. Ajayan

Catalysts ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 275 ◽  
Author(s):  
Miao Liu ◽  
Yanhui Yi ◽  
Li Wang ◽  
Hongchen Guo ◽  
Annemie Bogaerts

Due to the increasing emission of carbon dioxide (CO2), greenhouse effects are becoming more and more severe, causing global climate change. The conversion and utilization of CO2 is one of the possible solutions to reduce CO2 concentrations. This can be accomplished, among other methods, by direct hydrogenation of CO2, producing value-added products. In this review, the progress of mainly the last five years in direct hydrogenation of CO2 to value-added chemicals (e.g., CO, CH4, CH3OH, DME, olefins, and higher hydrocarbons) by heterogeneous catalysis and plasma catalysis is summarized, and research priorities for CO2 hydrogenation are proposed.


2020 ◽  
Vol 5 (2) ◽  
pp. 486-519 ◽  
Author(s):  
Vignesh Kumaravel ◽  
John Bartlett ◽  
Suresh C. Pillai

Molecules ◽  
2021 ◽  
Vol 26 (22) ◽  
pp. 6962
Author(s):  
Sulafa Abdalmageed Saadaldeen Mohammed ◽  
Wan Zaireen Nisa Yahya ◽  
Mohamad Azmi Bustam ◽  
Md Golam Kibria

The electrochemical reduction of carbon dioxide (CO2ER) is amongst one the most promising technologies to reduce greenhouse gas emissions since carbon dioxide (CO2) can be converted to value-added products. Moreover, the possibility of using a renewable source of energy makes this process environmentally compelling. CO2ER in ionic liquids (ILs) has recently attracted attention due to its unique properties in reducing overpotential and raising faradaic efficiency. The current literature on CO2ER mainly reports on the effect of structures, physical and chemical interactions, acidity, and the electrode–electrolyte interface region on the reaction mechanism. However, in this work, new insights are presented for the CO2ER reaction mechanism that are based on the molecular interactions of the ILs and their physicochemical properties. This new insight will open possibilities for the utilization of new types of ionic liquids. Additionally, the roles of anions, cations, and the electrodes in the CO2ER reactions are also reviewed.


Author(s):  
Pooja Srivastava

Despite its life-threatening long term effects, the continuous increase of carbon dioxide (CO2) in the environment requires immediate actions to control the accelerating climate change. An appealing solution to this problem is to utilize CO2 as feedstock to generate useful chemicals, e.g., fuel, hydrocarbons, and valuable chemicals. The chemical inertness of CO2 needs considerably large energy for its conversion into useful chemicals. Therefore, CO2 reduction reaction requires an effective catalyst for its conversion into fuel (methanol, methane) and industrial chemicals (syngas, formic acid). Recently, two-dimensional layers of early transition metal carbides and nitrides, called MXene, have shown potential for catalysis due to its exposed transition metal sites, and mechanical and chemical stability at high temperatures. Herein, the author presents the MXene as a potential heterogeneous catalyst for the CO2 reduction reaction (CRR), and the future scope in this currently developing field.


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