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EDITORIAL article

Front. Chem., 24 October 2023
Sec. Green and Sustainable Chemistry
Volume 11 - 2023 | https://doi.org/10.3389/fchem.2023.1310024

Editorial: CO2 capture and conversion: advanced materials and processes

www.frontiersin.orgZhangfeng Shen1* www.frontiersin.orgHuayang Zhang2 www.frontiersin.orgYangang Wang1
  • 1College of Biological Chemical Science and Engineering, Jiaxing University, Jiaxing, Zhejiang, China
  • 2School of Chemical Engineering and Advanced Materials, The University of Adelaide, Adelaide, Australia

The continuously increase of the atmospheric carbon dioxide (CO2) concentration have triggered global warming and climate change, and carbon neutrality is one of the most important target for human society. CO2 capture and conversion have become hot areas of research and development aimed at mitigating climate change and reducing greenhouse gas emissions. Advanced materials and processes play a crucial role in these efforts.

In CO2 capture, the goal is to capture CO2 emissions from various sources such as power plants, industrial processes, and transportation. Advanced materials like porous materials, membranes, and solvents are being developed to selectively capture CO2. These materials have high surface areas and specific properties that enable efficient CO2 adsorption and separation. Karolina form West Pomeranian University of Technology prepared carbonaceous materials from beet molasses through a hydrothermal process followed by chemical activation and used them for CO2 capture (Kielbasa). The activated biocarbon with a high specific surface area of 2005 m2g−1 and a total pore volume of 0.851 cm3g−1 gave the highest CO2 adsorption of 7.1 mmol/g at 1 bar and 0 °C.

Once CO2 is captured, it can be converted into valuable products through various processes. Advanced catalytic materials are being explored to convert CO2 into chemicals, fuels, and other useful products. For example, CO2 can be converted into methanol, which can be used as a fuel or as a feedstock for the production of other chemicals. Xu et al. from Jiangsu University prepared a Cu1In2Zr4-O-C catalyst with Cu2In alloy structure by sol–gel method and used for CO2 hydrogenation to methanol (Song et al.). They found the plasma treatment before or after calcination could improve the CO2 hydrogenation activity to some extent. Especially, a CO2 conversion of 13.3%, a methanol selectivity of 74.3%, and a CH3OH space-time yield of 3.26 mmol/gcat/h could be achieved on the catalyst of Cu1In2Zr4-O-PC, which was plasma-modified before calcination, under the conditions of reaction temperature 270 °C, reaction pressure 2 MPa, CO2/H2 = 1/3, and GHSV = 12,000 mL/(gh). This because the plasma modification can reduce the particle size, enhance the interaction between Cu and In, and shift the Cu 2p orbital binding energy to a lower position. It is expected that advanced technologies will make great contribution in the preparation of materials, which have high CO2 conversion efficiency and stability.

Electrochemical processes, such as electroreduction, are also being investigated for CO2 conversion. Cao et al. from Jiaxing University reviewed the recent progress of electrocatalytic CO2 reduction reaction (CO2RR) related to different types of single-atom catalysts (SACs) and double-atom catalysts (DACs) from the perspective of theoretical calculation (Meng et al.). They summarized different catalytic reaction mechanisms of SACs and DACs, and studied the influences of solvation and electrode potential on CO2RR to simulate the real electrochemical environment. In addition, they designed three types of Cu-based catalysts (Cu@CNTs, Cu4@CNTs, and CuNi3@CNTs) and compared their structure towards the activity of electrocatalytic CO2RR (An et al.). It was found that the CuNi3@CNTs show the largest CO2 adsorption energy (−0.82 eV), improving the CO2RR selectivity compared with hydrogen evolution, and the CO2RR product changes from CH4 to CO with a size increase from single-atom Cu to the Cu4 cluster. The Cu4@CNTs displayed an extremely low overpotential of 0.02 V for CO formation, while Cu@CNTs showed the highest selectivity for CH4 formation among the three catalysts. Theory and computation will play an important role in discovering new materials for CO2 conversion since the data-driven methods have been widely applied in material design.

In addition to materials, advanced processes are being developed to enhance the efficiency and scalability of CO2 capture and conversion technologies, although we did not receive relevant article in this Research Topic. These include process intensification, integration of renewable energy sources, and optimization of reaction conditions. It is noteworthy that while CO2 capture and conversion technologies have the potential to contribute to greenhouse gas reduction, they should be considered as part of a comprehensive strategy that includes energy efficiency, renewable energy deployment, and sustainable practices.

Despite the progress achieved to date, there is great need for further research to be conducted. For example, there is limited understanding of mechanism of interaction between CO2 and catalyst surface and more fundamental research is needed to achieve optimal catalyst designs, particularly those materials coupling with the kinetic and thermodynamic requirements of CO2 reduction. Overall, the development of advanced materials and processes for CO2 capture and conversion is an important step towards achieving a low-carbon and sustainable future.

Author contributions

ZS: Funding acquisition, Writing–original draft, Writing–review and editing. HZ: Formal Analysis, Writing–review and editing. YW: Funding acquisition, Writing–review and editing.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The authors acknowledge the financial support from National Natural Science Foundation of China (Grant No. 22278176), Zhejiang Provincial Natural Science Foundation of China (Grant No. LY19B060006 and LQ20E030016), Research Funding of Jiaxing University (Grant No. CD70517042), and Jiaxing Public Welfare Research Program Project (2023AY11018).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: CO2 capture, CO2 conversion, catalytic materials, theoretical calculation, advanced technologies

Citation: Shen Z, Zhang H and Wang Y (2023) Editorial: CO2 capture and conversion: advanced materials and processes. Front. Chem. 11:1310024. doi: 10.3389/fchem.2023.1310024

Received: 09 October 2023; Accepted: 16 October 2023;
Published: 24 October 2023.

Edited and reviewed by:

James Clark, University of York, United Kingdom

Copyright © 2023 Shen, Zhang and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Zhangfeng Shen, zfshen@mail.zjxu.edu.cn

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