Carbon-thin-layer protected WP with no passivation supported on acid-treated expanded graphite as efficient Pt Co-catalysts for methanol oxidation and oxygen reduction reactions. Issue 45 (31st October 2018)

• Record Type: Journal Article
• Authors: Zhang, Chunyue; Dai, Ying; Chen, Hun; Ma, Yuanyuan; Jing, Baojian; Cai, Zhuang; Duan, Yaqiang; Tang, Bo; Zou, Jinlong
• Is Part Of: Journal of materials chemistry. Volume 6:Issue 45(2018)
• Page Start: 22636
• Page End: 22644
• Publication Date: 2018-10-31
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8ta08285e
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Pt-WP-CL/AEG catalysts with particles-encapsulated layer-by-layer structure obtain high activity and durability for methanol oxidation and oxygen reduction reactions. Abstract : Application of direct methanol fuel cells (DMFCs) is hampered by the low activity, poor stability, and low CO/methanol tolerance of Pt-based catalysts used for methanol oxidation reaction (MOR)/oxygen reduction reaction (ORR). In this study, tungsten phosphide-embedded carbon-thin-layer/acid-treated expanded graphite (WP-CL/AEG) composites are synthesized as Pt-supports/co-catalysts for MOR/ORR via a one-step synthesis route. For MOR, Pt-WP-CL/AEG-3 (molar ratio of P to AEG is 3.6 in precursor) shows the highest electrochemical surface area (123.05 m 2 gPt −1 ) and mass activity (2217.6 mA mgPt −1 ), which are respectively 1.92 and 4.44 times higher than those of commercial Pt/C (64.16 m 2 gPt −1 and 499.2 mA mgPt −1 ). Pt-WP-CL/AEG catalysts also exhibit higher CO tolerance and stability than Pt/C. Moreover, Pt-WP-CL/AEG-3 also exhibits a higher ORR activity than Pt/C in acidic media, mainly via a 4e − transfer pathway (OH − as the main product) for ORR. As expected, AEG greatly enhances the charge transfer capacity of Pt-WP-CL/AEG catalysts; the exposed P active sites induced by W atoms on WP facilitate methanol/O2 adsorption and activation during MOR/ORR; the CL originated from citric acid can protect WP from being oxidized in air, which contributes to high activity and stability of P active sites; and charges are transferred from AEG (positively charged) to WP via the linked-CL and then from WP to Pt, which contributes to the high MOR/ORR activity of Pt-WP-CL/AEG. It indicates that WP-CL/AEGs can be considered as promising supports/co-catalysts for Pt in MOR/ORR.