NiFe Alloy Nanoparticles Tuning the Structure, Magnetism, and Application for Oxygen Evolution Reaction Catalysis

Author:

Raimundo Rafael A.12,Silva Vinícius D.3ORCID,Ferreira Luciena S.3,Loureiro Francisco J. A.4ORCID,Fagg Duncan P.4,Macedo Daniel A.3,Gomes Uílame U.5,Soares Márcio M.2ORCID,Gomes Rodinei M.1,Morales Marco A.6

Affiliation:

1. Department of Mechanical Engineering, Universidade Federal da Paraíba, João Pessoa 58051-900, Brazil

2. Department of Physics, Universidade Federal da Paraíba, João Pessoa 58051-900, Brazil

3. Department of Materials Science and Engineering, Universidade Federal da Paraíba, João Pessoa 58051-900, Brazil

4. Centre for Mechanical Technology and Automation, Department of Mechanical Engineering, University of Aveiro, 3810-193 Averio, Portugal

5. Department of Materials Science and Engineering, Universidade Federal do Rio Grande do Norte, Natal 59078-970, Brazil

6. Department of Physics, Universidade Federal do Rio Grande do Norte, Natal 59078-970, Brazil

Abstract

In this study, Ni-Fe alloy nanoparticles were prepared using the proteic sol–gel method, followed by a reduction in H2 at 500 and 700 °C, namely hereafter as NiFe-500 and NiFe-700, respectively. The morphological, structural, and magnetic properties were tuned via the thermal treatment in H2. The samples were studied using XPS, TEM, Mössbauer spectroscopy, DC magnetic measurements, and electrochemical measurements. Ritveld refinements showed that the sample NiFe-500 has FCC (face-centered cubic) and BCC (body-centered cubic) NiFe alloys, while the sample NiFe-700 has only FCC NiFe alloy. For both samples, magnetization measurements in the range of 300–900 K showed the presence of the Griffiths phase, indicating the formation of clusters of either Fe or Ni-Fe alloys rich in Fe. The sample NiFe-500 presented ferromagnetic (FM) transitions at 533, 700, and 834 K, assigned to the alloys Ni37Fe63-FCC, Ni46Fe54-FCC, and Ni55Fe45-FCC, respectively. In contrast, we could not observe the FM transition of the BCC Ni-Fe alloy because of limitations in our experimental setup (T ≤ 900 K). Meanwhile, three FM transitions were observed for the sample NiFe-700 at 480, 655, and 825 K, attributed to the alloys Ni34Fe66-FCC, Ni43Fe57-FCC, and Ni54Fe46-FCC, respectively. At 5 K, the samples NiFe-500 and NiFe-700 have saturation magnetizations of 164.2 and 173.6 emu g−1, respectively. For application in Oxygen Evolution Reaction catalysis, the samples NiFe-500 and NiFe-700 showed different overpotentials of 319 and 307 mV at 10 mA cm−2. These low overpotential values indicate a higher electrochemical activity of the FCC Ni-Fe alloy and, for both samples, a superior electrocatalytic activity in comparison to RuO2 e IrO2 conventional catalysts. Furthermore, the samples showed high electrochemical stability in chrono potentiometric studies for up to 15 h. This current work highlights that the Ni-Fe alloys produced via the proteic sol–gel and with a reduction in H2 methods can be promising for OER systems due to their good performance and low costs.

Funder

PORTUGAL 2020 Partnership Agreement through the European Regional Development Fund

Publisher

MDPI AG

Subject

Materials Chemistry,Chemistry (miscellaneous),Electronic, Optical and Magnetic Materials

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