Measurement Techniques for the Study of Thin Film Heterogeneous Water Oxidation Electrocatalysts

被引:524
作者
Stevens, Michaela Burke [1 ]
Enman, Lisa J. [1 ]
Batchellor, Adam S. [1 ]
Cosby, Monty R. [1 ]
Vise, Ashlee E. [1 ]
Trang, Christina D. M. [1 ]
Boettcher, Shannon W. [1 ]
机构
[1] Univ Oregon, Dept Chem & Biochem, Eugene, OR 97403 USA
基金
美国国家科学基金会;
关键词
OXYGEN EVOLUTION REACTION; TRANSITION-METAL (OXY)HYDROXIDES; ALKALINE ELECTROLYTES; OXIDE CATALYSTS; ELECTROCHEMICAL EVOLUTION; SURFACE OXIDATION; EVOLVING CATALYST; ENHANCED ACTIVITY; REDOX PROCESSES; COBALT OXIDE;
D O I
10.1021/acs.chemmater.6b02796
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
Heterogeneous electrocatalysts for the oxygen evolution reaction (OER) are complicated materials with dynamic structures. They can exhibit potential-induced phase transitions, potential-dependent electronic properties, variable oxidation and protonation states, and disordered local/surface phases. These properties make understanding the OER, and ultimately designing higher efficiency catalysts, challenging. We report a series of procedures and measurement techniques that we have adopted or developed to assess each of the above challenges in understanding materials for the OER. These include the targeted synthesis of hydrated oxyhydroxide phases, the assessment and elimination of electrolyte impurities, the use of a quartz crystal microbalance to monitor film loading and dissolution, and the use of an in situ conductivity measurement to understand the flow of electrons from the catalyst active sites to the conductive support electrode. We end with a recipe for the synthesis and characterization of a "standard" Ni(Fe)OxHy catalyst that can be performed in any laboratory with a basic electrochemical setup and used as a quantitative comparison to aid the development of new OER catalyst systems.
引用
收藏
页码:120 / 140
页数:21
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