System Design Rules for Intensifying the Electrochemical Reduction of CO2 to CO on Ag Nanoparticles

被引:117
作者
Bhargava, Saket S. [1 ,2 ]
Proietto, Federica [1 ,6 ]
Azmoodeh, Daniel [1 ]
Cofell, Emiliana R. [2 ,3 ]
Henckel, Danielle A. [1 ,2 ,4 ]
Verma, Sumit [1 ,2 ]
Brooks, Christopher J. [5 ]
Gewirth, Andrew A. [2 ,4 ]
Kenis, Paul J. A. [1 ,2 ]
机构
[1] Univ Illinois, Dept Chem & Biomol Engn, 600 S Mathews Ave, Urbana, IL 61801 USA
[2] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
[3] Univ Illinois, Dept Mat Sci & Engn, 1304 W Green St, Urbana, IL 61801 USA
[4] Univ Illinois, Dept Chem, 505 S Mathews Ave, Urbana, IL 61801 USA
[5] Honda Res Inst USA Inc, 1381 Kinnear Rd, Columbus, OH 43212 USA
[6] Univ Palermo, Dipartimento Ingn, 61 Piazza Marina, I-90133 Palermo, Italy
关键词
silver; nanoparticles; carbon dioxide electroreduction; electrolyte engineering; process intensification; SUPPORTING ELECTROLYTE CATION; ALKALI-METAL CATIONS; CARBON-DIOXIDE; ELECTROCATALYTIC REDUCTION; MECHANISTIC INSIGHTS; CU ELECTRODE; ELECTROREDUCTION; CATALYST; EFFICIENT; SILVER;
D O I
10.1002/celc.202000089
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electroreduction of CO2 (eCO(2)RR) is a potentially sustainable approach for carbon-based chemical production. Despite significant progress, performing eCO(2)RR economically at scale is challenging. Here we report meeting key technoeconomic benchmarks simultaneously through electrolyte engineering and process optimization. A systematic flow electrolysis study - performing eCO(2)RR to CO on Ag nanoparticles as a function of electrolyte composition (cations, anions), electrolyte concentration, electrolyte flow rate, cathode catalyst loading, and CO2 flow rate - resulted in partial current densities of 417 and 866 mA/cm(2) with faradaic efficiencies of 100 and 98 % at cell potentials of -2.5 and -3.0 V with full cell energy efficiencies of 53 and 43 %, and a conversion per pass of 17 and 36 %, respectively, when using a CsOH-based electrolyte. The cumulative insights of this study led to the formulation of system design rules for high rate, highly selective, and highly energy efficient eCO(2)RR to CO.
引用
收藏
页码:2001 / 2011
页数:11
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  • [1] The Impact of Specifically Adsorbed Ions on the Copper-Catalyzed Electroreduction of CO2
    Akhade, Sneha A.
    McCrum, Ian T.
    Janik, Michael J.
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2016, 163 (06) : F477 - F484
  • [2] Alper Erdogan, 2017, Petroleum, V3, P109, DOI 10.1016/j.petlm.2016.11.003
  • [3] Structure- and Electrolyte-Sensitivity in CO2 Electroreduction
    Aran-Ais, Rosa M.
    Gao, Dunfeng
    Roldan Cuenya, Beatriz
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2018, 51 (11) : 2906 - 2917
  • [4] Spectroscopic Evidence of Size-Dependent Buffering of Interfacial pH by Cation Hydrolysis during CO2 Electroreduction
    Ayemoba, Onagie
    Cuesta, Angel
    [J]. ACS APPLIED MATERIALS & INTERFACES, 2017, 9 (33) : 27377 - 27382
  • [5] Electrolyte Dependence of CO2 Electroreduction: Tetraalkylammonium Ions Are Not Electrocatalysts
    Berto, Timothy C.
    Zhang, Linghong
    Hamers, Robert J.
    Berry, John F.
    [J]. ACS CATALYSIS, 2015, 5 (02): : 703 - 707
  • [6] What Should We Make with CO2 and How Can We Make It?
    Bushuyev, Oleksandr S.
    De Luna, Phil
    Cao Thang Dinh
    Tao, Ling
    Saur, Genevieve
    van de lagemaat, Jao
    Kelley, Shana O.
    Sargent, Edward H.
    [J]. JOULE, 2018, 2 (05) : 825 - 832
  • [7] Cao-Thang D., 2019, JOULE, V3, P13
  • [8] Electric Field Effects in Electrochemical CO2 Reduction
    Chen, Leanne D.
    Urushihara, Makoto
    Chan, Karen
    Norskov, Jens K.
    [J]. ACS CATALYSIS, 2016, 6 (10): : 7133 - 7139
  • [9] Activation of CO2 at the electrode-electrolyte interface by a co-adsorbed cation and an electric field
    Chernyshova, Irina V.
    Ponnurangam, Sathish
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2019, 21 (17) : 8797 - 8807
  • [10] Opportunities and challenges for a sustainable energy future
    Chu, Steven
    Majumdar, Arun
    [J]. NATURE, 2012, 488 (7411) : 294 - 303