Unraveling the Electrocatalytic Activity in HMF Oxidation to FDCA by Fine‐Tuning the Degree of NiOOH Phase Over Ni Nanoparticles Supported on Graphene Oxide

Author:

Klinyod Sorasak1,Yodsin Nuttapon2,Nguyen Mai Thanh3,Pasom Zikkawas1,Assavapanumat Sunpet1,Ketkaew Marisa1,Kidkhunthod Pinit4,Yonezawa Tetsu3,Namuangruk Supawadee5,Wattanakit Chularat1ORCID

Affiliation:

1. Department of Chemical and Biomolecular Engineering School of Energy Science and Engineering Vidyasirimedhi Institute of Science and Technology Rayong 21210 Thailand

2. Department of Chemistry Faculty of Science Silpakorn University Nakorn Pathom 73000 Thailand

3. Division of Materials Science and Engineering Faculty of Engineering Hokkaido University Sapporo Hokkaido 060–8628 Japan

4. Synchrotron Light Research Institute (Public Organization) 111 University Avenue Muang Nakhon Ratchasima 30000 Thailand

5. National Nanotechnology Center (NANOTEC) National Science and Technology Development Agency Pathum Thani 12120 Thailand

Abstract

AbstractThe development of an efficient electrocatalyst for HMF oxidation to FDCA has been in the early stages. Herein, the NiNPs/GO‐Ni‐foam is fabricated as an electrocatalyst for FDCA production. However, the electrocatalytic performance of the untreated NiNPs/GO‐Ni‐foam is observed with moderate Faradaic efficiency (FE) (73.0%) and FDCA yield (80.2%). By electrochemically treating the NiNPs/GO‐Ni‐foam in an alkaline solution with positive potential at different treatment durations, the degree of NiOOH on metal surfaces is changed. The distinctive electrocatalytic activity obtained when using the different NiOOH degrees allows to understand the crucial impact of NiOOH species in HMF electrooxidation. Enhancing the portion of the NiOOH phase on the electrocatalyst surface improves electrocatalytic activity in terms of FE and FDCA yield up to 94.8±4.8% and 86.9±4.1%, respectively. Interestingly, as long as the NiOOH portion on the electrocatalyst surface is preserved or regenerated, the electrocatalyst performance can be intact even after several catalytic cycles. The theoretical study via density functional theory (DFT) also agrees with the experimental observations and confirms that the NiOOH phase facilitates the electrochemical transformation of HMF to FDCA through the HMFCA pathway, and the potential limiting step of the overall reaction is the oxidation of FFCA to FDCA.

Funder

National Research Council of Thailand

Vidyasirimedhi Institute of Science and Technology

Thailand Science Research and Innovation

Publisher

Wiley

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