Journal
ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 38, Pages 35410-35419Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b09942
Keywords
superhydrophobic; hydrogen peroxide (H2O2); oxygen reduction reaction (ORR); polytetrafluoroethylene (PTFE); air-breathing cathode
Funding
- National Natural Science Foundation of China [51778408, 21577068]
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Electrochemical catalysis of carbon-based material via two-electron pathway oxygen reduction reaction (ORR) offers great potential for in situ hydrogen peroxide (H2O2) production. In this work, we tuned catalyst mesostructure and hydrophilicity/hydrophobicity by adjusting polytetrafluoroethylene (PTFE) content in graphite/carbon black/PTFE hybrid catalyst layer (CL), aimed to improving the two-electron ORR activity for efficient H2O2 generation. As the only superhydrophobic CL with initiating contact angles of 141.11 degrees, PTFE0.57 obtained the highest H2O2 yield of 3005 +/- 58 mg L-1 h(-1) (at 25 mA cm(-2)) and highest current efficiency (CE) of 84% (at 20 mA cm(-2)). Rotating ring disk electrode (RRDE) results demonstrated that less PTFE content in CLs results in less electrons transferred and better selectivity toward two-electron ORR Though the highest H-2 concentration (2 mu mol L-1 at 25 mA cm(-2)) was monitored from PTFE0.57 which contained the lowest PTFE, the CE decreased inversely with increasing content of PTFE, which proved that the H2O2 decomposition reaction was the major side reaction. Higher PTFE content increased the hydrophilicity of CL for excessive H+ and insufficient O-2 diffusion, which induced H2O2 decomposition into H2O. Simultaneously, the electroactive surface area of CLs decreased with higher PTFE content, from 0.0041 m(2) g(-1) of PTFE0.57 to 0.0019 m(2 )g(-1) of PTFE4.56. Besides, higher PTFE content in CL leads to the increase of total impedance (from 14.5 Omega of PTFE0.57 to 18.3 Omega of PTFE4.56), which further hinders the electron transfer and ORR activity.
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