CaSnO3: An Electrocatalyst for Two-Electron Water Oxidation Reaction to Form H2O2

被引:169
作者
Park, So Yeon [1 ,2 ]
Abroshan, Hadi [3 ]
Shi, Xinjian [2 ]
Jung, Hyun Suk [1 ]
Siahrostami, Samira [3 ]
Zheng, Xiaolin [2 ]
机构
[1] Sungkyunkwan Univ, Sch Adv Mat Sci & Engn, Suwon 16419, South Korea
[2] Stanford Univ, Dept Mech Engn, 440 Escondido Mall, Stanford, CA 94305 USA
[3] Stanford Univ, SUNCAT Ctr Interface Sci & Catalysis, Dept Chem Engn, 443 Via Ortega, Stanford, CA 94305 USA
基金
新加坡国家研究基金会;
关键词
HYDROGEN-PEROXIDE PRODUCTION; ELECTRONIC-STRUCTURES; OXYGEN REDUCTION; PEROVSKITE; CATALYSTS; EFFICIENT;
D O I
10.1021/acsenergylett.8b02303
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 two-electron water oxidation reaction (2e-WOR) is a promising route for distributed electrochemical synthesis of hydrogen peroxide (H2O2), an effective and green oxidizer, bleaching agent, and antiseptic. To date, the best electrocatalyst for 2e-WOR, in terms of selectivity against the competing 4e-WOR to form O-2, is BiVO4. Nevertheless, BiVO4 is unstable and has a high overpotential of similar to 340 mV at 0.2 mA/cm(2) for 2e-WOR. Herein, we use density functional theory to identify a new, efficient, selective, and stable electrocatalyst for 2e-WOR, i.e., the ternary oxide calcium stannate (CaSnO3). Our experiments show that CaSnO3 achieves an overpotential of 230 mV at 0.2 mA/cm(2), peak Faraday efficiency of 76% for 2e-WOR at 3.2 V vs the reversible hydrogen electrode (RHE), and stable performance for over 12 h, outperforming BiVO4 in all aspects. This work demonstrates the promise of CaSnO3 as a selective and cost-effective electrocatalyst candidate for H2O2 production from water oxidation.
引用
收藏
页码:352 / 357
页数:11
相关论文
共 24 条
  • [1] [Anonymous], 1985, Standard potential in aqueous solutions
  • [2] Selectivity of cobalt-based catalysts towards hydrogen peroxide formation during the reduction of oxygen
    Campos, Maria
    Siriwatcharapiboon, Wilai
    Potter, Robert J.
    Horswell, Sarah L.
    [J]. CATALYSIS TODAY, 2013, 202 : 135 - 143
  • [3] Two-Electron Oxygen Reduction on Carbon Materials Catalysts: Mechanisms and Active Sites
    Chai, Guo-Liang
    Hou, Zhufeng
    Ikeda, Takashi
    Terakura, Kiyoyuki
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2017, 121 (27) : 14524 - 14533
  • [4] Defective BiFeO3 with surface oxygen vacancies: Facile synthesis and mechanism insight into photocatalytic performance
    Chen, Da
    Niu, Feng
    Qin, Laishun
    Wang, Sen
    Zhang, Ning
    Huang, Yuexiang
    [J]. SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2017, 171 : 24 - 32
  • [5] Development of a reactor with carbon catalysts for modular-scale, low-cost electrochemical generation of H2O2
    Chen, Zhihua
    Chen, Shucheng
    Siahrostami, Samira
    Chakthranont, Pongkarn
    Hahn, Christopher
    Nordlund, Dennis
    Dimosthenis, Sokaras
    Norskov, Jens K.
    Bao, Zhenan
    Jaramillo, Thomas F.
    [J]. REACTION CHEMISTRY & ENGINEERING, 2017, 2 (02): : 239 - 245
  • [6] Fierro J. L. G., 2005, Metal oxides: Chemistry and applications, DOI DOI 10.1021/ja065737o
  • [7] WO3/BiVO4 photoanode coated with mesoporous Al2O3 layer for oxidative production of hydrogen peroxide from water with high selectivity
    Fuku, Kojiro
    Miyase, Yuta
    Miseki, Yugo
    Gunji, Takahiro
    Sayama, Kazuhiro
    [J]. RSC ADVANCES, 2017, 7 (75): : 47619 - 47623
  • [8] Enhanced Oxidative Hydrogen Peroxide Production on Conducting Glass Anodes Modified with Metal Oxides
    Fuku, Kojiro
    Miyase, Yuta
    Miseki, Yugo
    Gunji, Takahiro
    Sayama, Kazuhiro
    [J]. CHEMISTRYSELECT, 2016, 1 (18): : 5721 - 5726
  • [9] Efficient oxidative hydrogen peroxide production and accumulation in photoelectrochemical water splitting using a tungsten trioxide/bismuth vanadate photoanode
    Fuku, Kojiro
    Sayama, Kazuhiro
    [J]. CHEMICAL COMMUNICATIONS, 2016, 52 (31) : 5406 - 5409
  • [10] Surface Pourbaix diagrams and oxygen reduction activity of Pt, Ag and Ni(111) surfaces studied by DFT
    Hansen, Heine A.
    Rossmeisl, Jan
    Norskov, Jens K.
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2008, 10 (25) : 3722 - 3730