Abstract
Well-designed electronic configurations and structural properties of electrocatalyst alter the activity, stability, and mass transport for enhanced catalytic reactions. We introduce a nanofibrous oxide-carbon composite by an in situ method of carbon nanofiber (CNF) growth by highly dispersed Ni nanoparticles that are exsoluted from a NiTiO3 surface. The nanofibrous feature has a 3D web structure with improved mass-transfer properties at the electrode. In addition, the design of the CNF/TiO2 support allows for complex properties for excellent stability and activity from the TiO2 oxide support and high electric conductivity through the connected CNF, respectively. Developed CNF/TiO2-Pt nanofibrous catalyst displays exemplary oxygen-reduction reaction (ORR) activity with significant improvement of the electrochemical surface area. Moreover, exceptional resistance to carbon corrosion and Pt dissolution is proven by durability-test protocols based on the Department of Energy. These results are well-reflected to the single-cell tests with even-better performance at the kinetic zone compared to the commercial Pt/C under different operation conditions. CNF/TiO2-Pt displays an enhanced active state due to the strong synergetic interactions, which decrease the Pt d-band vacancy by electron transfer from the oxide-carbon support. A distinct reaction mechanism is also proposed and eventually demonstrates a promising example of an ORR electrocatalyst design.
Original language | English |
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Pages (from-to) | 6819-6829 |
Number of pages | 11 |
Journal | ACS Nano |
Volume | 12 |
Issue number | 7 |
DOIs | |
Publication status | Published - 2018 Jul 24 |
Bibliographical note
Funding Information:This work was funded by the Ministry of Science, ICT, and Future Planning Technology through the Development Program to Solve Climate Changes of the National Research Foundation (NRF) (grant no. NRF-2015M1A2A2056833). This work was also supported by the Technology Innovation Industrial Program funded by the Ministry of Trade, Industry and Energy (MOTIE), Republic of Korea (grant no. 10052823).
Funding Information:
This work was funded by the Ministry of Science, ICT, and Future Planning Technology through the Development Program to Solve Climate Changes of the National Research Foundation (NRF) (grant no. NRF-2015M1A2A2056833). This work was also supported by the Technology Innovation Industrial Program funded by the Ministry of Trade, Industry, and Energy (MOTIE), Republic of Korea (grant no. 10052823).
Publisher Copyright:
© 2018 American Chemical Society.
All Science Journal Classification (ASJC) codes
- Materials Science(all)
- Engineering(all)
- Physics and Astronomy(all)