A catalyst design for selective electrochemical reactions: direct production of hydrogen peroxide in advanced electrochemical oxidation

Hydrogen peroxide production by enhanced electrocatalysts is an attractive alternative to the present commercial process. While the subnano/atomic dispersion in noble metal nanocatalysts is known to strongly enhance their catalytic efficiency and chemoselectivity, their excessive surface energy and...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-01, Vol.8 (19), p.9859-987
Hauptverfasser: Ko, Young-Jin, Choi, Keunsu, Yang, Boram, Lee, Woong Hee, Kim, Jun-Yong, Choi, Jae-Woo, Chae, Keun Hwa, Lee, Jun Hee, Hwang, Yun Jeong, Min, Byoung Koun, Oh, Hyung-Suk, Lee, Wook-Seong
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Sprache:eng
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Zusammenfassung:Hydrogen peroxide production by enhanced electrocatalysts is an attractive alternative to the present commercial process. While the subnano/atomic dispersion in noble metal nanocatalysts is known to strongly enhance their catalytic efficiency and chemoselectivity, their excessive surface energy and consequent coarsening seriously compromise their physical/chemical stability. Here, we report a subnano/atomically dispersed Pt-Ag alloy (by a simply modified polyol process) that is resistant to agglomeration/Ostwald ripening. This catalyst does not follow a conventional four-electron oxygen reduction reaction (ORR) but selectively produces H 2 O 2 without excessive degradation of its activity. We clarified the role of the alloying element, Ag, as follows: (1) selective activation of two-electron ORR by inhibiting O 2 dissociation and (2) suppression of H 2 O 2 decomposition by preventing the H 2 O 2 adsorption. The present approach provides a convenient route for the direct generation of H 2 O 2 as a simple byproduct of electricity generation by fuel-cell systems. Hydrogen peroxide production by enhanced electrocatalysts is an attractive alternative to the present commercial process.
ISSN:2050-7488
2050-7496
DOI:10.1039/d0ta01869d