物理化学学报 >> 2023, Vol. 39 >> Issue (5): 2212027.doi: 10.3866/PKU.WHXB202212027

综述 上一篇    

二氧化碳电催化还原中的电解质效应

荣佑文1,2, 桑佳琪2,3, 车丽1,*(), 高敦峰2,*(), 汪国雄2   

  1. 1 大连海事大学理学院, 辽宁 大连, 116026
    2 中国科学院大连化学物理研究所, 催化基础国家重点实验室, 辽宁 大连, 116023
    3 中国科学院大学, 北京 100049
  • 收稿日期:2022-12-16 录用日期:2023-01-02 发布日期:2023-01-09
  • 通讯作者: 车丽,高敦峰 E-mail:liche@dlmu.edu.cn;dfgao@dicp.ac.cn
  • 基金资助:
    国家重点研发计划(2021YFA1501503);国家自然科学基金(22002155);国家自然科学基金(21973010);国家自然科学基金(22125205);国家自然科学基金(92045302);中科院战略性先导专项(XDA21061010);辽宁省兴辽英才计划(XLYC1907032);辽宁省自然科学基金(2021-MS-022);大连化物所创新基金(DICP I202203)

Designing Electrolytes for Aqueous Electrocatalytic CO2 Reduction

Youwen Rong1,2, Jiaqi Sang2,3, Li Che1,*(), Dunfeng Gao2,*(), Guoxiong Wang2   

  1. 1 School of Science, Dalian Maritime University, Dalian 116026, Liaoning Province, China
    2 State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning Province, China
    3 University of Chinese Academy of Sciences, Beijing 100049, China
  • Received:2022-12-16 Accepted:2023-01-02 Published:2023-01-09
  • Contact: Li Che, Dunfeng Gao E-mail:liche@dlmu.edu.cn;dfgao@dicp.ac.cn
  • Supported by:
    the National Key R & D Program of China(2021YFA1501503);National Natural Science Foundation of China(22002155);National Natural Science Foundation of China(21973010);National Natural Science Foundation of China(22125205);National Natural Science Foundation of China(92045302);Strategic Priority Research Program of the Chinese Academy of Sciences(XDA21061010);Liao Ning Revitalization Talents Program, China(XLYC1907032);Natural Science Foundation of Liaoning Province, China(2021-MS-022);the Dalian Institute of Chemical Physics, China(DICP I202203)

摘要:

二氧化碳(CO2)电催化还原反应利用可再生能源将CO2转化为高值燃料和化学品,是一种新型的碳中和技术。CO2电催化还原反应在电极/电解质界面上进行,因此除催化剂以外,电解质对提高CO2电催化还原反应性能同样至关重要。本文深度剖析了CO2电催化还原反应中的电解质效应,结合近几年的最新研究进展,详细讨论了局部pH、阳离子、阴离子和离子交换膜等电解质组成和性质对电催化活性和产物选择性的影响,阐述了电解质效应的催化作用机制。本文特别强调了电化学原位红外/拉曼等振动光谱在电解质效应机理研究方面的优势以及面向实际应用的膜电极CO2电解器中阴离子、阳离子、水、液体产物等物质传输对活性、选择性、能量效率及CO2利用效率等关键催化性能指标的影响。本文最后提出了当前电解质效应研究中存在的挑战,并展望了未来的研究机遇和发展趋势。

关键词: CO2电催化还原, 电解质效应, 双电层, pH效应, 阳离子效应, 阴离子效应, 固体聚合物电解质, 膜电极

Abstract:

As an emerging technology for achieving carbon neutrality, the electrocatalytic CO2 reduction reaction (CO2RR) converts CO2 and water to valuable fuels and chemicals with power supply from renewable energy. Currently, the practical application of the CO2RR suffers from insufficient electrocatalytic performance in terms of selectivity, reaction rate, energy efficiency, and long-term stability. Electrolytes are considered as equally critical as catalysts for enhancing the CO2RR performance. From a catalysis perspective, electrolytes significantly affect the reaction microenvironments around catalytically active sites. From an electrochemical perspective, electrolytes determine the electric double layer structure. The electrocatalytic electrode/electrolyte interface where the CO2RR takes place is strongly influenced by electrolyte composition and identity. Thus, beyond catalyst design, rational electrolyte design is an alternative strategy for advancing the CO2RR towards industrial applications. This review presents important electrolyte effects in the aqueous CO2RR using the most recent studies, with an emphasis on those conducted under industrially-relevant reaction conditions. The effects of (local) pH, cations, and anions in aqueous inorganic electrolytes and their coupled effects with solid polymer electrolytes on tuning the activity and selectivity of the CO2RR are summarized. Although their influences on CO2RR performance are interconnected, pH effects, cation effects, and anion effects as well as electrolyte effects in membrane electrode assembly (MEA) electrolyzers are discussed separately considering the leading role of each factor. The experimentally observed performance dependence on the electrolyte composition and identity as well as the underlying reaction mechanism are discussed. The unique role of vibrational spectroscopies, such as surface-enhanced infrared absorption and Raman, in the characterization of electrode/electrolyte interfaces and the elucidation of electrolyte effects is highlighted. An innovative experimental strategy that involves the validation of specific adsorption of alkali-metal cations on the surface of an electrode by precisely monitoring the vibrational spectroscopic characteristics of probe molecules is highly recommended. The review focuses on the pH-dependent electrocatalytic performance and reaction pathways, the uncertain mechanisms of cation effects, and the roles of typical anions, such as bicarbonate and halides. Particularly, emphasis is given to the transport of key species, such as anions, cations, water, and products in ion exchange membranes, as well as their dynamic behaviors at the electrode/electrolyte interface in MEA CO2 electrolyzers. Although it has some drawbacks, anion exchange membranes are currently the most promising polymer electrolytes for practical application of the CO2RR. However, some emerging strategies based on cation exchange and bipolar membranes as well as tandem electrolysis processes are in progress. In all cases, a detailed understanding of electrolyte effects in the complex environments of MEA electrolyzers is indispensable for achieving performance enhancement. In conclusion, the remaining challenges and research opportunities in terms of the experimental and theoretical investigation of the electrolyte effects in the CO2RR process are proposed. This review provides novel insights into rational electrolyte design and useful guidelines for researchers in the field.

Key words: Electrocatalytic CO2 electroreduction, Electrolyte effect, Electric double layer, pH effect, Cation effect, Anion effect, Solid polymer electrolyte, Membrane electrode assembly