Enhanced electrocatalytic performance of Pt nanoparticles on triazine-functionalized graphene nanoplatelets for both oxygen and iodine reduction reactions. Issue 41 (12th October 2017)

• Record Type: Journal Article
• Authors: Jeon, In-Yup; Kweon, Do Hyung; Kim, Seong-Wook; Shin, Sun-Hee; Im, Yoon Kwang; Yu, Soo-Young; Ju, Myung Jong; Baek, Jong-Beom
• Is Part Of: Journal of materials chemistry. Volume 5:Issue 41(2017)
• Page Start: 21936
• Page End: 21946
• Publication Date: 2017-10-12
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c7ta06912j
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Triazine-functionalized graphene nanoplatelets were synthesized for use as platinum nanoparticle supports. The Pt/TfGnP catalyst exhibited high electrocatalytic activity with superb stability for both the ORR and IRR. Abstract : Platinum (Pt) nanoparticles were stably anchored on triazine-functionalized graphene nanoplatelets (TfGnPs), which were prepared by a two-step reaction starting from carboxylic acid- (CGnPs), acyl chloride- (AcGnPs) and amide-functionalized graphene nanoplatelets (AfGnPs). The resulting Pt nanoparticles on TfGnPs (Pt/TfGnPs) exhibited outstanding electrocatalytic activity with significantly enhanced stability compared with commercial Pt-based catalysts for the oxygen reduction reaction (ORR) in fuel cells (FCs) and the iodine reduction reaction (IRR) in dye-sensitized solar cells (DSSCs). For the ORR in FCs, the onset and half-wave potentials of Pt/TfGnPs under acidic conditions displayed greater positive shifts to 0.58 and 0.53 V, respectively, than those of the commercial Pt/C catalyst (0.57 and 0.52 V). For the IRR in DSSCs, Pt/TfGnPs displayed a reduced charge transfer resistance ( R ct ) of 0.13 Ω cm 2 at the CE/electrolyte interface. This value was much lower than the Pt CE of 0.52 Ω cm 2 . More importantly, Pt/TfGnPs exhibited profoundly improved electrochemical stability in both the ORR and IRR compared to the Pt-based catalysts. The combination of extraordinarily high electrocatalytic activity with stability could be attributed to the high specific surface area (963.0 m 2 g −1 ) and the triazine units of the TfGnPs, respectively, which provided more active sites and stably anchored the Pt nanoparticles.