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|Title:||1-Naphthol induced Pt3Ag nanocorals as bifunctional cathode and anode catalysts of direct formic acid fuel cells||Authors:||Jiang, Xian
|Keywords:||Engineering::Chemical engineering||Issue Date:||2019||Source:||Jiang, X., Liu, Y., Wang, J., Wang, Y., Xiong, Y., Liu, Q., Li, N., Zhou, J., Fu, G., Sun, D. & Tang, Y. (2019). 1-Naphthol induced Pt3Ag nanocorals as bifunctional cathode and anode catalysts of direct formic acid fuel cells. Nano Research, 12(2), 323-329. https://dx.doi.org/10.1007/s12274-018-2218-2||Journal:||Nano Research||Abstract:||Developing highly efficient bifunctional cathode and anode electrocatalysts is very important for the large-scale application of direct formic acid fuel cells. However, the high-cost and poor CO-tolerance ability of the most commonly used Pt greatly block this process. To increase the utilization efficiency and extend bifunctional properties of precious Pt, herein, coral-like Pt3Ag nanocrystals are developed as an excellent bifunctional electrocatalyst through a facile one-pot solvothermal method. The formation mechanism of Pt3Ag nanocorals has been elaborated well via a series of control experiments. It is proved that 1-naphthol serving as a guiding surfactant plays a key role in the formation of high-quality nanocorals. Thanks to the unique coral-like structure and alloy effects, the developed Pt3Ag nanocorals present significantly enhanced electrocatalytic properties (including activity, stability and CO-tolerance ability) towards both the cathodic oxygen reduction and anodic formic acid oxidation, as compared with those of commercial Pt black and Pt-based nanoparticles. The present synthetic method can also be extended to fabricate other bimetallic electrocatalysts with unique morphology and structure.||URI:||https://hdl.handle.net/10356/151345||ISSN:||1998-0124||DOI:||10.1007/s12274-018-2218-2||Rights:||© 2018 Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature. All rights reserved.||Fulltext Permission:||none||Fulltext Availability:||No Fulltext|
|Appears in Collections:||SCBE Journal Articles|
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