Pd nanoparticles deposited on Co(OH)2 nanoplatelets as a bifunctional electrocatalyst and their application in Zn–air and Li–O2 batteries

The development of affordable electrocatalysts for both oxygen reduction and evolution reactions (ORR/OER) has received great interest due to their importance in metal–air batteries and regenerative fuel cells. We developed a high-performance bifunctional oxygen electrocatalyst based on Pd nanoparti...

Full description

Saved in:
Bibliographic Details
Published inNanoscale Vol. 12; no. 34; pp. 17858 - 17869
Main Authors Suyeon Hyun, Saejio, Apichat, Shanmugam, Sangaraju
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 01.01.2020
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The development of affordable electrocatalysts for both oxygen reduction and evolution reactions (ORR/OER) has received great interest due to their importance in metal–air batteries and regenerative fuel cells. We developed a high-performance bifunctional oxygen electrocatalyst based on Pd nanoparticles supported on cobalt hydroxide nanoplatelets (Pd/Co(OH)2) as an air cathode for metal–air batteries. The Pd/Co(OH)2 shows remarkably higher electrocatalytic activity in comparison with commercial catalysts (Pt/C, IrO2), including an ORR half-wave potential (E1/2) of 0.87 V vs. RHE and an OER overpotential of 0.39 V at 10 mA cm−2 in aqueous alkaline medium. The Zn–air battery constructed with Pd/Co(OH)2 presents stable charge/discharge voltage (ΔEOER–ORR = 0.69 V), along with durable cycling stability for over 30 h. Also, this cathode exhibits a maximum discharge capacity of 17 698 mA h g−1, and stable battery operation over 50 cycles at a fixed capacity of 1000 mA h g−1, as an efficient air electrode for Li–O2 batteries, indicating that Pd/Co(OH)2 can be a potential candidate for both aqueous and non-aqueous metal–air batteries.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2040-3364
2040-3372
DOI:10.1039/d0nr05403h