Nickel telluride as a bifunctional electrocatalyst for efficient water splitting in alkaline medium

• Published in: Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (17), p.768-7622
• Main Authors: De Silva, Umanga, Masud, Jahangir, Zhang, Ning, Hong, Yu, Liyanage, Wipula P. R, Asle Zaeem, Mohsen, Nath, Manashi
• Format: Article
• Language: English
• Subjects: Activation; Anions; Catalysis; Catalysts; Catalytic activity; Chalcogenides; Electrocatalysts; Electrochemistry; Electrolysis; Electronegativity; Hypotheses; Intermetallic compounds; Metals; Nickel; Oxidation; Oxides; Renewable energy; Splitting; Stoichiometry; Surface stability; Sustainability; Tellurides; Water splitting
• ISSN: 2050-7488; 2050-7496
• DOI: 10.1039/c8ta01760c

Designing efficient electrocatalysts has been one of the primary goals for water electrolysis, which is one of the most promising routes towards sustainable energy generation from renewable sources. In this article, we have tried to expand the family of transition metal chalcogenide based highly efficient OER electrocatalysts by investigating nickel telluride, Ni 3 Te 2 as a catalyst for the first time. Interestingly Ni 3 Te 2 electrodeposited on a GC electrode showed very low onset potential and overpotential at 10 mA cm −2 (180 mV), which is the lowest in the series of chalcogenides with similar stoichiometry, Ni 3 E 2 (E = S, Se, Te) as well as Ni-oxides. This observation falls in line with the hypothesis that increasing the covalency around the transition metal center enhances catalytic activity. Such a hypothesis has been previously validated in oxide-based electrocatalysts by creating anion vacancies. However, this is the first instance where this hypothesis has been convincingly validated in the chalcogenide series. The operational stability of the Ni 3 Te 2 electrocatalyst surface during the OER for an extended period of time in alkaline medium was confirmed through surface-sensitive analytical techniques such as XPS, as well as electrochemical methods which showed that the telluride surface did not undergo any corrosion, degradation, or compositional change. More importantly we have compared the catalyst activation step (Ni 2+ → Ni 3+ oxidation) in the chalcogenide series, through electrochemical cyclic voltammetry studies, and have shown that catalyst activation occurs at lower applied potential as the electronegativity of the anion decreases. From DFT calculations we have also shown that the hydroxyl attachment energy is more favorable on the Ni 3 Te 2 surface compared to the Ni-oxide, confirming the enhanced catalytic activity of the telluride. Ni 3 Te 2 also exhibited efficient HER catalytic activity in alkaline medium making it a very effective bifunctional catalyst for full water splitting with a cell voltage of 1.66 V at 10 mA cm −2 . It should be noted here that this is the first report of OER and HER activity in the family of Ni-tellurides. Ni 3 Te 2 has been reported as a highly efficient OER electrocatalyst with an overpotential of 180 mV at 10 mA cm −2 and also showing HER catalytic activity in alkaline medium.