Mixed Metal Oxide Electrodes and the Chlorine Evolution Reaction

被引:70
作者
Dong, Heng [1 ]
Yu, Weilai [2 ]
Hoffmann, Michael R. [1 ]
机构
[1] CALTECH, Linde Labs, Pasadena, CA 91125 USA
[2] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
关键词
SURFACE HYDROXYL-GROUPS; ELECTROCATALYTIC OXYGEN EVOLUTION; ACTIVE CHLORINE; DEACTIVATION MECHANISM; ZERO CHARGE; ELECTROCHEMICAL TREATMENT; CORROSION MECHANISM; RUO2-TIO2/TI ANODES; RUTHENIUM DIOXIDE; AQUEOUS-SOLUTION;
D O I
10.1021/acs.jpcc.1c05671
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The chlorine evolution reaction (CER) has practical applications in the chlor-alkali industry and electrochemical wastewater treatment. Efficient, stable, and cost-effective electrodes are critical for energy efficient chlorine production, water disinfection, and wastewater treatment. These practical applications require an indepth understanding of the catalytic mechanism of chlorine evolution, the need for lower-cost electrode materials, and improvements in electrode design at the atomic scale. Herein, we examine factors controlling activity, selectivity, and stability of alternative CER electrodes and provide mechanistic insights for achieving improvements in performance and durability. Steric effects of crystal structure and intermetallic electron polarization provide insights for understanding and tuning the electrode activity and selectivity. Additional insight into electrode deactivation mechanisms was gained by employing model material systems under controlled conditions. Herein, we explore viable strategies for the development of more efficient noble-metal-free CER electrodes for use in a variety of practical applications.
引用
收藏
页码:20745 / 20761
页数:17
相关论文
共 164 条
[1]   An investigation of the effect of RuO2 on the deactivation and corrosion mechanism of a Ti/IrO2 + Ta2O5 coating in an OER application [J].
Abbasi, H. Mazhari ;
Jafarzadeh, K. ;
Mirali, S. M. .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2016, 777 :67-74
[2]   Selective Chlorine Evolution Catalysts Based on Mg-Doped Nanoparticulate Ruthenium Dioxide [J].
Abbott, Daniel F. ;
Petrykin, Valery ;
Okube, Maki ;
Bastl, Zdenk ;
Mukerjee, Sanjeev ;
Krtil, Petr .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2015, 162 (01) :H23-H31
[3]   SURFACE-PROPERTIES OF RUO2+IRO2 MIXED-OXIDE ELECTRODES [J].
ANGELINETTA, C ;
TRASATTI, S ;
ATANASOSKA, LD ;
ATANASOSKI, RT .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1986, 214 (1-2) :535-546
[4]  
[Anonymous], 2012, Aquatic Chemistry: Chemical Equilibria and Rates in Natural Waters
[5]   Simultaneous determination of chlorine and oxygen evolving at RuO2/Ti and RuO2-TiO2/Ti anodes by differential electrochemical mass spectroscopy [J].
Arikawa, T ;
Murakami, Y ;
Takasu, Y .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1998, 28 (05) :511-516
[6]   IrO2 Coated on RuO2 as Efficient and Stable Electroactive Nanocatalysts for Electrochemical Water Splitting [J].
Audichon, Thomas ;
Napporn, Teko W. ;
Canaff, Christine ;
Morais, Claudia ;
Comminges, Clement ;
Kokoh, K. Boniface .
JOURNAL OF PHYSICAL CHEMISTRY C, 2016, 120 (05) :2562-2573
[7]   Electroactivity of RuO2-IrO2 mixed nanocatalysts toward the oxygen evolution reaction in a water electrolyzer supplied by a solar profile [J].
Audichon, Thomas ;
Mayousse, Eric ;
Morisset, Sophie ;
Morais, Claudia ;
Comminges, Clement ;
Napporn, Teko W. ;
Kokoh, K. Boniface .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2014, 39 (30) :16785-16796
[8]   Structural and optoelectronic properties of antimony incorporated tin oxide thin films [J].
Babar, A. R. ;
Shinde, S. S. ;
Moholkar, A. V. ;
Bhosale, C. H. ;
Kim, J. H. ;
Rajpure, K. Y. .
JOURNAL OF ALLOYS AND COMPOUNDS, 2010, 505 (02) :416-422
[9]   THE INVENTION AND INDUSTRIAL-DEVELOPMENT OF METAL ANODES [J].
BEER, HB .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1980, 127 (08) :C303-C307
[10]   The interaction of metal oxide surfaces with complexing agents dissolved in water [J].
Blesa, MA ;
Weisz, AD ;
Morando, PJ ;
Salfity, JA ;
Magaz, GE ;
Regazzoni, AE .
COORDINATION CHEMISTRY REVIEWS, 2000, 196 :31-63