Organic ligand-free PtIr alloy nanostructures for superior oxygen reduction and evolution reactions
Journal of Industrial and Engineering Chemistry, ISSN: 1226-086X, Vol: 77, Page: 105-110
2019
- 12Citations
- 5Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Article Description
In the thermal decomposition method, organic solvents, ligands, and compounds are usually used under an N 2 atmosphere to synthesize pure metal and alloy nanostructures with high specific surface areas. However, the organic materials, which are used during the synthesis of metallic nanostructures, need to be completely eliminated to obtain cleaned surface states for effective catalytic reactions in aqueous atmospheres. Herein, we synthesize PtIr nanostructures using a thermal decomposition method, followed by a heating process of the nanostructures under an air atmosphere to eliminate the organic materials covering the surface of PtIr catalysts. The heated PtIr alloy nanostructure catalysts represent the superior oxygen reduction and evolution performance due to an increased electrochemical active surface area caused by the complete removal of organic materials.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1226086X1930187X; http://dx.doi.org/10.1016/j.jiec.2019.04.024; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85064914302&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S1226086X1930187X; https://dx.doi.org/10.1016/j.jiec.2019.04.024
Elsevier BV
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