An Efficient and Durable Electrocatalyst Based on Strongly Coupled Pt Nanoparticles on CeO2 Microspheres for CO-Resilient Methanol Oxidation

催化作用 甲醇 纳米颗粒 化学工程 材料科学 电催化剂 环境友好型 溶剂 复合数 热液循环 金属 纳米技术 化学 有机化学 电极 复合材料 冶金 物理化学 工程类 生物 电化学 生态学
作者
Paskalis Sahaya Murphin Kumar,Subramanian Arulmani,Hyoung‐il Kim,D Ramakrishnan,Vinoth Kumar Ponnusamy,Umapada Pal,Siva Kumar Krishnan
出处
期刊:Journal of Physical Chemistry C [American Chemical Society]
卷期号:126 (44): 18670-18682 被引量:16
标识
DOI:10.1021/acs.jpcc.2c05069
摘要

Designing durable, highly active supported Pt catalysts has attracted tremendous interest in recent years due to their high electrocatalytic activities and stability in methanol oxidation reactions (MORs). Herein, we report an eco-friendly synthetic strategy for obtaining Pt/CeO2 composite microspheres, which are highly active and durable catalysts for MOR. The porous CeO2 microspheres were prepared through a hydrothermal method using the Piper longum fruit extract, which is an environmentally friendly solvent. The Pt nanoparticles (NPs) with an average size of ∼5 nm dispersed on CeO2 microspheres were obtained by the chemical reduction of Pt2+ ions at room temperature. It was found that the supported Pt NPs are strongly coupled through strong metal–support interactions (SMSIs), which promoted the formation of oxygen vacancies (OVs) and increased the concentration of active Ce3+ sites. Owing to the presence of high OVs and of Ce3+ species, the Pt/CeO2 microsphere catalyst revealed enhanced MOR performance, with specific activity (SA) as high as 36.37 mA/cm2 and mass activity (MA) of 229.44 mA/mg, which are substantially higher than those of commercial catalysts such as Pt/C and Pt/CeO2 prepared with commercial CeO2 nanoparticles. Moreover, the resultant catalyst showed excellent durability, retaining about 76.2% of its initial current density even after 5000 potential cycles. The used green extract-mediated synthesis process can be a promising alternative to conventional methods for the rational design of highly active metal nanoparticle-supported catalysts for heterogeneous catalysts.
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