PtCu Nanoparticle Catalyst for Electrocatalytic Glycerol Oxidation: How Does the PtCu Affect to Glycerol Oxidation Reaction Performance by Changing pH Conditions?

Author:

Oh Lee Seul12,Han Jeonghyun3,Lim Eunho1ORCID,Kim Won Bae3,Kim Hyung Ju14ORCID

Affiliation:

1. Chemical & Process Technology Division, Korea Research Institute of Chemical Technology (KRICT), 141 Gajeong-ro, Yuseong-gu, Daejeon 34114, Republic of Korea

2. Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Republic of Korea

3. Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), 77 Cheongam-ro, Nam-gu, Pohang 37673, Republic of Korea

4. Advanced Materials and Chemical Engineering, University of Science and Technology (UST), 113 Gwahangno, Yuseong-gu, Daejeon 34113, Republic of Korea

Abstract

In this work, we show that finding and controlling optimum pH environments with Pt-based alloy catalysts can create high catalytic performances for electrocatalytic glycerol oxidation reaction (EGOR). Compared to a Pt/C catalyst, the PtCu/C alloy catalyst has higher reaction rate and turnover frequency (TOF) values by increasing the pH. Specifically, the reaction rate and TOF of the PtCu/C catalyst at pH 13 were 2.93 and 6.65 times higher than those of Pt/C, respectively. The PtCu/C catalyst also showed lower onset potential value and higher mass and specific activities than the Pt/C by increasing the pH. This indicates that the Cu in the PtCu alloy improves the catalytic activity for the EGOR in an OH− group-rich environment. In the case of the PtCu/C catalyst at a high pH condition, the selectivities of tartronic acid and oxalic acid tended to increase as the selectivity of lactic acid decreased. This result means that the PtCu alloy follows primary alcohol oxidation pathways, which are more favorable in an OH− group-rich environment than with only Pt. This study proposes that it is critical to optimize and control the reaction conditions for developing efficient EGOR catalysts.

Funder

National Research Foundation of Korea

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis,General Environmental Science

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