Objective: Iridium oxide films are commonly used as a high charge-injection electrode material in neural devices. Yet, few studies have performed in-depth assessments of material performance versus film thickness, especially for films grown on three-dimensional (instead of planar) metal surfaces in neutral pH electrolyte solutions. Further, few studies have investigated the driving voltage requirements for constant-current stimulation using activated iridium oxide (AIROF) electrodes, which will be a key constraint for future use in wirelessly powered neural devices.
Approach: In this study, iridium microwire probes were activated by repeated potential pulsing in room temperature phosphate buffered saline (pH 7.1-7.3). Electrochemical measurements were recorded in three different electrolyte conditions for probes with different geometric surface areas (GSAs) as the AIROF thickness was increased.
Main Results: Maintaining an anodic potential bias during the inter-pulse interval was required for AIROF electrodes to deliver charge levels considered necessary for neural stimulation. Potential pulsing for 100-200 cycles was sufficient to achieve charge injection levels of 2.5 mC cm (50 nC/phase in a biphasic pulse) in PBS with 2000 µm iridium probes. Increasing the electrode surface area to 3000 µm and 4000 µm significantly increased charge-injection capacity, reduced the driving voltage required to deliver a fixed amount of charge, and reduced polarization of the electrodes during constant-current pulsing.
Significance: This study establishes methods for choosing an activation protocol and a desired GSA for three-dimensional iridium electrodes suitable for neural tissue insertion and stimulation, and provides guidelines for evaluating electrochemical performance of AIROF using model saline solutions.
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http://dx.doi.org/10.1088/1741-2552/abb9bf | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Institute of Materials Research, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, Guangdong, PR China.
Resolving the atomic surface structure, particularly surface termination or reconstruction, is essential for understanding the catalytic properties of metal oxides. Although rutile phase iridium dioxide (IrO) is the state-of-the-art electrocatalyst for the oxygen evolution reaction (OER) in water splitting, the atomic-level surface structures of IrO remain largely unexplored, limiting our understanding of its facet-dependent OER activities. Herein, we perform aberration-corrected integrated differential phase contrast scanning transmission electron microscopy of the low- and high-index surface structures of spindle-shaped IrO nanorods and reveal distinct surface terminations and/or reconstructions on different surfaces.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Institute of Functional Nano and Soft Materials (FUNSOM), Soochow University, Suzhou, 215123, China.
Developing durable IrO-based electrocatalysts with high oxygen evolution reaction (OER) activity under acidic condition is crucial for proton exchange membrane electrolyzers. While oxygen defects are considered potentially important in OER, their direct relationship with catalytic activity has yet to be established. In this study, we introduced abundant oxygen vacancies through Re doping in 2D IrO (ReIrO), demonstrating their decisive role in enhancing OER performance.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Jiangsu, 215123, P. R. China.
Anodic oxygen evolution reaction (OER) exhibits a sluggish four-electron transfer process, necessitating catalysts with exceptional catalytic activity to enhance its kinetic rate. Van der Waals layered oxides are ideal materials for catalyst design, yet its stability for acidic OER remains large obstacle. Doping provides a crucial way to improve the activity and stability simultaneously.
View Article and Find Full Text PDFScience
January 2025
School of Chemical Engineering, Sichuan University, Chengdu, China.
The iridium oxide (IrO) catalyst for the oxygen evolution reaction used industrially (in proton exchange membrane water electrolyzers) is scarce and costly. Although ruthenium oxide (RuO) is a promising alternative, its poor stability has hindered practical application. We used well-defined extended surface models to identify that RuO undergoes structure-dependent corrosion that causes Ru dissolution.
View Article and Find Full Text PDFSmall
December 2024
College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan, Shanxi, 030024, P. R. China.
Ruthenium oxide (RuO) is considered one of the most promising catalysts for replacing iridium oxide (IrO) in the acidic oxygen evolution reaction (OER). Nevertheless, the performance of RuO remains unacceptable due to the dissolution of Ru and the lack of *OH in acidic environments. This paper reports a grain boundary (GB)-rich porous RuO electrocatalyst for the efficient and stable acidic OER.
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