The current status of high temperature electrochemistry-based CO2 transport membranes and reactors for direct CO2 capture and conversion

IF 32 1区 工程技术 Q1 ENERGY & FUELS
Peng Zhang , Jingjing Tong , Kevin Huang , Xuefeng Zhu , Weishen Yang
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引用次数: 32

Abstract

The concept of direct CO2 capture and conversion has attracted significant interest from industries and academia in recent decades due to its potential to address the current grand challenge of global warming/climate change, rapid depletion of fossil fuels and realization of a future carbon neutral ecosystem. The incumbent benchmark technology for CO2 capture is the post-combustion flue-gas “amine washing”, which is energy intensive and costly for large-scale commercial implementation. The CO2 conversion technologies, on the other hand, are still at their infancy with many technical challenges to overcome, but primarily being explored in laboratory-scale, low-temperature, solution-based and high-temperature, solid-oxide-based electrochemical cells with renewable electricity perceived as the energy input. In this article, we provide a comprehensive overview on an emergent class of high-temperature electrochemical CO2 transport membranes that can capture and convert CO2 into valuable chemicals in single catalytic reactor fashion. The review starts with the chemistry and transport theory of three basic types of membranes purposely designed for different CO2 feedstocks and downstream conversions. A range of key functional materials used in these membranes and their microstructural/electrochemical properties important to the CO2 transport are then thoroughly discussed in conjunction with the effects of surface modifications and operating conditions. Several types of combined CO2 capture and conversion catalytic reactors based on these membranes are also assessed with a focus on their working principles, system configurations and performance demonstrations. Finally, challenges and prospective of these electrochemical CO2 transport membranes and their associated conversion reactors are candidly discussed for future development.

介绍了基于高温电化学的CO2传输膜及直接捕获和转化CO2的反应器的研究现状
近几十年来,二氧化碳直接捕获和转化的概念引起了工业界和学术界的极大兴趣,因为它有可能解决当前全球变暖/气候变化、化石燃料迅速枯竭和实现未来碳中和生态系统的巨大挑战。目前二氧化碳捕获的基准技术是燃烧后烟气“胺洗涤”,这是一种能源密集型技术,对于大规模商业实施来说成本高昂。另一方面,二氧化碳转换技术仍处于起步阶段,有许多技术挑战需要克服,但主要是在实验室规模上进行探索,低温,溶液和高温,固体氧化物为基础的电化学电池,可再生电力被视为能量输入。在这篇文章中,我们全面概述了一种新兴的高温电化学CO2传输膜,它可以在单催化反应器中捕获并将CO2转化为有价值的化学物质。本文首先介绍了针对不同的CO2原料和下游转化而设计的三种基本类型的膜的化学和输运理论。然后,结合表面修饰和操作条件的影响,深入讨论了这些膜中使用的一系列关键功能材料及其对二氧化碳传输至关重要的微结构/电化学性能。本文还对几种基于这些膜的组合式CO2捕获和转化催化反应器进行了评估,重点介绍了它们的工作原理、系统配置和性能演示。最后,对这些电化学CO2传输膜及其相关转化反应器的发展前景进行了展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Progress in Energy and Combustion Science
Progress in Energy and Combustion Science 工程技术-工程:化工
CiteScore
59.30
自引率
0.70%
发文量
44
审稿时长
3 months
期刊介绍: Progress in Energy and Combustion Science (PECS) publishes review articles covering all aspects of energy and combustion science. These articles offer a comprehensive, in-depth overview, evaluation, and discussion of specific topics. Given the importance of climate change and energy conservation, efficient combustion of fossil fuels and the development of sustainable energy systems are emphasized. Environmental protection requires limiting pollutants, including greenhouse gases, emitted from combustion and other energy-intensive systems. Additionally, combustion plays a vital role in process technology and materials science. PECS features articles authored by internationally recognized experts in combustion, flames, fuel science and technology, and sustainable energy solutions. Each volume includes specially commissioned review articles providing orderly and concise surveys and scientific discussions on various aspects of combustion and energy. While not overly lengthy, these articles allow authors to thoroughly and comprehensively explore their subjects. They serve as valuable resources for researchers seeking knowledge beyond their own fields and for students and engineers in government and industrial research seeking comprehensive reviews and practical solutions.
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