Self-Assembly of Copper Oxide Interfaced MnO2 for Oxygen Evolution Reaction

Author:

Bathula Chinna1,Meena Abhishek2,Sekar Sankar34ORCID,Singh Aditya Narayan5ORCID,Soni Ritesh6ORCID,El-Marghany Adel7,Palem Ramasubba Reddy8ORCID,Kim Hyun-Seok1ORCID

Affiliation:

1. Division of Electronics and Electrical Engineering, Dongguk University–Seoul, Seoul 04620, Republic of Korea

2. Division of Physics and Semiconductor Science, Dongguk University-Seoul, Seoul 04620, Republic of Korea

3. Department of Semiconductor Science, Dongguk University-Seoul, Seoul 04620, Republic of Korea

4. Quantum-Functional Semiconductor Research Center, Dongguk University-Seoul, Seoul 04620, Republic of Korea

5. Department of Energy and Materials Engineering, Dongguk University-Seoul, Seoul 04620, Republic of Korea

6. Department of Chemical Engineering, Department of Energy Engineering, Ulsan National Institute of Science and Technology (UNIST), 50 UNIST-gil, Ulsan 44919, Republic of Korea

7. Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia

8. Department of Medical Biotechnology, Dongguk University, 32 Dongguk-ro, Ilsandong-gu, Goyang 10326, Republic of Korea

Abstract

Designing efficient electrocatalytic systems through facile synthesis remains a formidable task. To address this issue, this paper presents the design of a combination material comprising two transition metal oxides (copper oxide and manganese oxide (CuO/MnO2)), synthesized using a conventional microwave technique to efficiently engage as an active oxygen evolution reaction (OER) catalyst. The structural and morphological properties of the composite were confirmed by the aid of X-ray diffraction (XRD) studies, field emission scanning electron microscopy (FESEM), X-ray photoelectron spectroscopy (XPS), and energy-dispersive spectrometry (EDS). FESEM clearly indicated well-aligned interlacing of CuO with MnO2. The OER performance was carried out in 1 M KOH. The assembled CuO/MnO2 delivered a benchmark current density (j = 10 mA cm−2) at a minimal overpotential (η = 294 mV), while pristine CuO required a high η (316 mV). Additionally, the CuO/MnO2 electrocatalyst exhibited stability for more than 15 h. These enhanced electrochemical performances were attributed to the large volume and expanded diameter of the pores, which offer ample surface area for catalytic reactions to boost OER. Furthermore, the rate kinetics of the OER are favored in composite due to low Tafel slope (77 mV/dec) compared to CuO (80 mV/dec).

Funder

Ministry of Science and ICT

Dongguk University

King Saud University

Publisher

MDPI AG

Subject

General Materials Science,General Chemical Engineering

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