Elucidating the alkaline oxygen evolution reaction mechanism on platinum

被引:133
作者
Favaro, M. [1 ,2 ,3 ]
Valero-Vidal, C. [1 ,4 ]
Eichhorn, J. [3 ]
Toma, F. M. [3 ]
Ross, P. N. [5 ]
Yano, J. [2 ,6 ]
Liu, Z. [7 ,8 ]
Crumlin, E. J. [1 ,4 ]
机构
[1] Lawrence Berkeley Natl Lab, Adv Light Source, One Cyclotron Rd, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Joint Ctr Artificial Photosynth, One Cyclotron Rd, Berkeley, CA 94720 USA
[3] Lawrence Berkeley Natl Lab, Chem Sci Div, One Cyclotron Rd, Berkeley, CA 94720 USA
[4] Lawrence Berkeley Natl Lab, Joint Ctr Energy Storage Res, One Cyclotron Rd, Berkeley, CA 94720 USA
[5] Lawrence Berkeley Natl Lab, Div Mat Sci, One Cyclotron Rd, Berkeley, CA 94720 USA
[6] Lawrence Berkeley Natl Lab, Mol Biophys & Integrated Bioimaging Div, One Cyclotron Rd, Berkeley, CA 94720 USA
[7] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, State Key Lab Funct Mat Informat, Shanghai 200050, Peoples R China
[8] ShanghaiTech Univ, Sch Phys Sci & Technol, Div Condensed Matter Phys & Photon Sci, Shanghai 200031, Peoples R China
基金
中国国家自然科学基金;
关键词
RAY PHOTOELECTRON-SPECTROSCOPY; AMBIENT-PRESSURE XPS; ELECTRON-SPECTRA; PT(111) SURFACE; DOUBLE-LAYER; FUEL-CELLS; OXIDATION; CATALYSTS; REDUCTION; ELECTROCATALYSIS;
D O I
10.1039/c7ta00409e
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
Understanding the interplay between surface chemistry, electronic structure, and reaction mechanism of the catalyst at the electrified solid/liquid interface will enable the design of more efficient materials systems for sustainable energy production. The substantial progress in operando characterization, particularly using synchrotron based X-ray spectroscopies, provides the unprecedented opportunity to uncover surface chemical and structural transformations under various (electro)chemical reaction environments. In this work, we study a polycrystalline platinum surface under oxygen evolution conditions in an alkaline electrolyte by means of ambient pressure X-ray photoelectron spectroscopy performed at the electrified solid/liquid interface. We elucidate previously inaccessible aspects of the surface chemistry and structure as a function of the applied potential, allowing us to propose a reaction mechanism for oxygen evolution on a platinum electrode in alkaline solutions.
引用
收藏
页码:11634 / 11643
页数:10
相关论文
共 64 条
[1]  
[Anonymous], 2006, ANGEW CHEM-GER EDIT, DOI DOI 10.1002/ANGE.200504386
[2]  
Arrigo R., 2013, ANGEW CHEM INT EDIT, V52, P1
[3]   Using "Tender" X-ray Ambient Pressure X-Ray Photoelectron Spectroscopy as A Direct Probe of Solid-Liquid Interface [J].
Axnanda, Stephanus ;
Crumlin, Ethan J. ;
Mao, Baohua ;
Rani, Sana ;
Chang, Rui ;
Karlsson, Patrik G. ;
Edwards, Marten O. M. ;
Lundqvist, Mans ;
Moberg, Robert ;
Ross, Phil ;
Hussain, Zahid ;
Liu, Zhi .
SCIENTIFIC REPORTS, 2015, 5
[4]   Thermodynamic explanation of the universal correlation between oxygen evolution activity and corrosion of oxide catalysts [J].
Binninger, Tobias ;
Mohamed, Rhiyaad ;
Waltar, Kay ;
Fabbri, Emiliana ;
Levecque, Pieter ;
Koetz, Ruediger ;
Schmidt, Thomas J. .
SCIENTIFIC REPORTS, 2015, 5
[5]   OXYGEN EVOLUTION AT PLATINUM-ELECTRODES IN ALKALINE-SOLUTIONS .1. DEPENDENCE ON SOLUTION PH AND OXIDE FILM THICKNESS [J].
BIRSS, VI ;
DAMJANOVIC, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1987, 134 (01) :113-117
[6]   CHANGES IN THE KINETICS OF THE OXYGEN EVOLUTION REACTION INDUCED BY OXIDE-FILMS AT PLATINUM-ELECTRODES [J].
BOLZAN, AE ;
ARVIA, AJ .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1994, 375 (1-2) :157-162
[7]   INTERLAYER MASS-TRANSPORT IN HOMOEPITAXIAL AND HETEROEPITAXIAL METAL GROWTH [J].
BROMANN, K ;
BRUNE, H ;
RODER, H ;
KERN, K .
PHYSICAL REVIEW LETTERS, 1995, 75 (04) :677-680
[8]   MICROSCOPIC VIEW OF NUCLEATION ON SURFACES [J].
BRUNE, H ;
RODER, H ;
BORAGNO, C ;
KERN, K .
PHYSICAL REVIEW LETTERS, 1994, 73 (14) :1955-1958
[9]   The Study of Reactive Intermediates in Condensed Phases [J].
Carpenter, Barry K. ;
Harvey, Jeremy N. ;
Orr-Ewing, Andrew J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (14) :4695-4705
[10]  
Carrette L, 2001, FUEL CELLS, V1, P5, DOI 10.1002/1615-6854(200105)1:1<5::AID-FUCE5>3.0.CO