Mechanistic Insights into the Role of Elements in Ni‐Co‐P Catalysts for Electrochemical Conversion of 5‐Hydroxymethylfurfural to 2,5‐Furandicarboxylic Acid

Author:

Woo Jongin12,Choi Jinu3,Choi Juhyung4,Lee Mi‐Young1,Kim Eunji1,Yun Sang15,Yoo Suhwan4,Lee Eunchong4,Lee Ung12,Won Da Hye156,Park Jong Hyeok7,Hwang Yun Jeong48,Yoo Jong Suk3ORCID,Lee Dong Ki1257ORCID

Affiliation:

1. Clean Energy Research Center Korea Institute of Science and Technology Seoul 02792 Republic of Korea

2. Graduate School of Energy and Environment Korea University Seoul 02841 Republic of Korea

3. Department of Chemical Engineering University of Seoul Seoul 02504 Republic of Korea

4. Department of Chemistry Seoul National University Seoul 08826 Republic of Korea

5. Division of Energy and Environmental Technology KIST School, Korea University of Science and Technology (UST) Seoul 02792 Republic of Korea

6. KHU‐KIST Department of Converging Science and Technology Kyung Hee University Seoul 02477 Republic of Korea

7. Department of Chemical and Biomolecular Engineering Yonsei‐KIST Convergence Research Institute Yonsei University Seoul 03722 Republic of Korea

8. Center for Nanoparticle Research, Institute for Basic Science (IBS) Seoul 08826 Republic of Korea

Abstract

AbstractNi phosphides and NiCo alloys are extensively explored for their remarkable efficiency in biomass alcohol oxidations, yet the underlying mechanisms remain inadequately understood. This study thoroughly elucidates the roles of Ni, Co, and P in improving the catalytic performance of Ni‐Co‐P catalysts for the electrochemical conversion of 5‐hydroxymethylfurfural (HMF) to 2,5‐furandicarboxylic acid (FDCA), a promising biomass‐derived building block replacing terephthalic acid. Phosphorization of Ni results in the partial formation of Ni2P phase and significantly boosts the formation of the reactive NiOOH phase on the surface, which is the crucial catalytic phase for converting HMF into FDCA. The integration of Co into the heterojunction between Ni2P and NiOOH enhances the oxidation reactivity of 5‐formyl‐2‐furancarboxylic acid (FFCA), a pivotal intermediate influencing FDCA productivity, by selectively stabilizing aldehydes, thereby promoting further oxidation rather than surface desorption. in situ/operando spectroscopic analyses consistently highlight the equal significance of the rapid generation of NiOOH and the robust adsorption of reactant molecules at the surface in achieving high catalytic performance. These insights into elemental contributions set a new standard for designing multi‐component electrocatalysts for efficient biomass alcohol oxidation.

Funder

National Research Foundation of Korea

Korea Institute of Science and Technology

Ministry of Science and ICT, South Korea

University of Seoul

Publisher

Wiley

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