期刊
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 23, 期 33, 页码 17904-17916出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cp02370e
关键词
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资金
- University of Rochester [CHE-1900125]
- U.S. National Science Foundation [CHE-1900125]
- U.S. Department of Energy, Office of Science, Office of Workforce Development for Teachers and Scientists, Office of Science Graduate Student Research (SCGSR) program
- DOE [DE-SC0014664]
- NSF MRI grant [CHE-1725028]
This paper describes the analysis of dropcast nanocrystalline and electrochemically deposited films of NiO and alpha-Fe2O3 as model metal oxide semiconductors immersed in redox-inactive organic electrolyte solutions using EIS. The interpretation of physical meaning of circuit elements differs from EIS measurements of metal oxide electrodes immersed in redox-active media. Understanding the distinction between film morphology and intrinsic electronic structure of the metal oxide is crucial for evaluating nanostructured metal oxide electrodes for electrochemical energy storage and electrocatalysis applications.
This paper describes analysis of dropcast nanocrystalline and electrochemically deposited films of NiO and alpha-Fe2O3 as model metal oxide semiconductors immersed in redox-inactive organic electrolyte solutions using electrochemical impedance spectroscopy (EIS). Although the data reported here fit a circuit commonly used to model EIS data of metal oxide electrodes, which comprises an RC circuit nested inside a second RC circuit that is in series with a resistor, our interpretation of the physical meaning of these circuit elements differs from that applied to EIS measurements of metal oxide electrodes immersed in redox-active media. The data presented here are most consistent with an interpretation in which the nested RC circuit represents charge transfer between the metal oxide film and the underlying metal electrode, and the non-nested RC circuit represents the resistance and capacitance associated with formation of a charge-compensating double-layer at the exposed interface between the metal electrode and electrolyte solution. Applying this interpretation to analysis of EIS data collected for metal oxide films in organic media enables the impact of film morphology on electrochemical behavior to be distinguished from the effects of the intrinsic electronic structure of the metal oxide. This distinction is crucial to the evaluation of nanostructured metal oxide electrodes for electrochemical energy storage and electrocatalysis applications.
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