Ultrathin dendritic IrTe nanotubes for an efficient oxygen evolution reaction in a wide pH range
Abstract
The shape control of Ir-based nanostructured materials, which are considered as the state-of-the-art anode electrocatalyst candidates toward the oxygen evolution reaction (OER), has been rarely reported. In this study, we reported an efficient synthesis of ultrathin dendritic IrTe nanotubes (NTs) via a galvanic replacement reaction using Te nanowires as the template at 190 °C for 1 h. The as-obtained IrTe NTs exhibited improved electrocatalytic activity and stability toward the OER with a much smaller overpotential of 290 mV and Tafel slope of 60.3 mV dec–1 to attain a current density of 10 mA cm–2 in acidic medium, compared with commercial IrO2 nanoparticles. Moreover, IrTe NTs also demonstrated enhanced electrocatalytic performances in neutral and alkaline media. The outstanding electrochemical properties of IrTe NTs in a wide pH range hold great promise in energy storage and conversion devices.
- Authors:
-
- Washington State Univ., Pullman, WA (United States)
- Washington State Univ., Pullman, WA (United States); Central China Normal Univ., Wuhan (China)
- Shandong Univ., Jinan (China)
- Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Environmental Molecular Sciences Lab. (EMSL)
- Publication Date:
- Research Org.:
- Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Environmental Molecular Sciences Lab. (EMSL)
- Sponsoring Org.:
- USDOE Office of Science (SC), Biological and Environmental Research (BER)
- OSTI Identifier:
- 1770580
- Report Number(s):
- PNNL-SA-130853
Journal ID: ISSN 2050-7488
- Grant/Contract Number:
- AC05-76RL01830
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Journal of Materials Chemistry. A
- Additional Journal Information:
- Journal Volume: 6; Journal Issue: 19; Journal ID: ISSN 2050-7488
- Publisher:
- Royal Society of Chemistry
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
Citation Formats
Shi, Qiurong, Zhu, Chengzhou, Du, Dan, Wang, Jin, Xia, Haibing, Engelhard, Mark H., Feng, Shuo, and Lin, Yuehe. Ultrathin dendritic IrTe nanotubes for an efficient oxygen evolution reaction in a wide pH range. United States: N. p., 2018.
Web. doi:10.1039/c8ta01288a.
Shi, Qiurong, Zhu, Chengzhou, Du, Dan, Wang, Jin, Xia, Haibing, Engelhard, Mark H., Feng, Shuo, & Lin, Yuehe. Ultrathin dendritic IrTe nanotubes for an efficient oxygen evolution reaction in a wide pH range. United States. https://doi.org/10.1039/c8ta01288a
Shi, Qiurong, Zhu, Chengzhou, Du, Dan, Wang, Jin, Xia, Haibing, Engelhard, Mark H., Feng, Shuo, and Lin, Yuehe. Mon .
"Ultrathin dendritic IrTe nanotubes for an efficient oxygen evolution reaction in a wide pH range". United States. https://doi.org/10.1039/c8ta01288a. https://www.osti.gov/servlets/purl/1770580.
@article{osti_1770580,
title = {Ultrathin dendritic IrTe nanotubes for an efficient oxygen evolution reaction in a wide pH range},
author = {Shi, Qiurong and Zhu, Chengzhou and Du, Dan and Wang, Jin and Xia, Haibing and Engelhard, Mark H. and Feng, Shuo and Lin, Yuehe},
abstractNote = {The shape control of Ir-based nanostructured materials, which are considered as the state-of-the-art anode electrocatalyst candidates toward the oxygen evolution reaction (OER), has been rarely reported. In this study, we reported an efficient synthesis of ultrathin dendritic IrTe nanotubes (NTs) via a galvanic replacement reaction using Te nanowires as the template at 190 °C for 1 h. The as-obtained IrTe NTs exhibited improved electrocatalytic activity and stability toward the OER with a much smaller overpotential of 290 mV and Tafel slope of 60.3 mV dec–1 to attain a current density of 10 mA cm–2 in acidic medium, compared with commercial IrO2 nanoparticles. Moreover, IrTe NTs also demonstrated enhanced electrocatalytic performances in neutral and alkaline media. The outstanding electrochemical properties of IrTe NTs in a wide pH range hold great promise in energy storage and conversion devices.},
doi = {10.1039/c8ta01288a},
journal = {Journal of Materials Chemistry. A},
number = 19,
volume = 6,
place = {United States},
year = {Mon Apr 02 00:00:00 EDT 2018},
month = {Mon Apr 02 00:00:00 EDT 2018}
}
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