Selective Electrochemical Generation of Hydrogen Peroxide from Water Oxidation

被引:156
作者
Viswanathan, Venkatasubramanian [1 ,3 ]
Hansen, Heine A. [2 ,3 ]
Norskov, Jens K. [3 ,4 ]
机构
[1] Carnegie Mellon Univ, Dept Mech Engn, Pittsburgh, PA 15213 USA
[2] Tech Univ Denmark, Dept Energy Convers & Storage, DK-2800 Lyngby, Denmark
[3] Stanford Univ, Dept Chem Engn, SUNCAT Ctr Interface Sci & Catalysis, Stanford, CA 94305 USA
[4] SLAC Natl Accelerator Lab, SUNCAT Ctr Interface Sci & Catalysis, Menlo Pk, CA 94025 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2015年 / 6卷 / 21期
关键词
OXYGEN EVOLUTION ELECTROCATALYSIS; GAS-DIFFUSION ELECTRODE; METAL-SURFACES; OXIDE SURFACES; REDUCTION; TRENDS; ANTHRAQUINONE; DISINFECTION; UNIVERSALITY; CHALLENGES;
D O I
10.1021/acs.jpclett.5b02178
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
Water is a life-giving source, fundamental to human existence, yet over a billion people lack access to clean drinking water. The present techniques for water treatment such as piped, treated water rely on time and resource intensive centralized solutions. In this work, we propose a decentralized device concept that can utilize sunlight to split water into hydrogen and hydrogen peroxide. The hydrogen peroxide can oxidize organics while the hydrogen bubbles out. In enabling this device, we require 2 an electrocatalyst that can oxidize water while suppressing the thermodynamically favored oxygen evolution and form hydrogen peroxide. Using density functional theory calculations, we show that the free energy of adsorbed OH* can be used to determine selectivity trends between the 2e(-) water oxidation to H2O2 and the 4e(-) oxidation to O-2. We show that materials which bind oxygen intermediates sufficiently weakly, such as SnO2, can activate hydrogen peroxide evolution. We present a rational design principle for the selectivity in electrochemical water oxidation and identify new material candidates that could perform H2O2 evolution selectively.
引用
收藏
页码:4224 / 4228
页数:5
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