Electrocatalytic ammonia production from nitrite via dual-site Co3O4/NiO catalysts derived from laser-induced cyanonickelate frameworks
- Authors
- Begildayeva, Talshyn; Theerthagiri, Jayaraman; Min, Ahreum; Moon, Cheol Joo; Choi, Myong Yong
- Issue Date
- Apr-2024
- Publisher
- Elsevier BV
- Keywords
- Ammonia synthesis; Co<sub>3</sub>O<sub>4</sub>/NiO; CoNi coordination polymer frameworks; Electrochemical nitrite reduction; Pulsed laser irradiation in liquids
- Citation
- Chemical Engineering Journal, v.485
- Indexed
- SCIE
SCOPUS
- Journal Title
- Chemical Engineering Journal
- Volume
- 485
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/69999
- DOI
- 10.1016/j.cej.2024.150041
- ISSN
- 1385-8947
1873-3212
- Abstract
- Herein, we report the pioneering synthesis of the cobalt–nickel coordination frameworks (Co(H2O)2·Ni(CN)4, CoNi-CF) via pulsed laser irradiation in liquids (PLIL). The distinctive morphology of CoNi-CF has attracted considerable attention as a potential template to produce Co3O4/NiO composites with varying Co and Ni ratios. After subjecting CoNi-CF to a high-temperature calcination process at 400 °C, the resulting Co3O4/NiO composites displayed dual-active canters for efficient electrochemical nitrite (NO2−) reduction to ammonia (NH3). Optimizing the Co:Ni ratio at 1:0.75 yielded Co3O4/NiO with exceptional performance, achieving a remarkable 99.4 % Faradaic efficiency in NH3 production while maintaining a 96.1 % mass balance at −1.2 V vs. Ag/AgCl. Furthermore, this composite displayed long-term stability, degrading 60.82 % of NO2− in 180 min, with high NH3 yield rate (2012.03 μM h−1 cm−2) at −1.6 V vs. Ag/AgCl. The superior performance in NO2− reduction to NH3 can be attributed to the unique structural features inherited from CoNi-CF, including well-defined and self-standing Co3O4 and NiO phases. Synergistic effects at the oxide interface enhance electrochemical performance and facilitate efficient charge transfer kinetics of Co3O4/NiO, underscoring the unique potential of these composite materials. © 2024 Elsevier B.V.
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