Alves Daniele, Moral Rafael A, Jayakumari Darshana, Dempsey Eithne, Breslin Carmel B
Department of Chemistry, Maynooth University, Maynooth, Co. Kildare Ireland, W23 F2H6.
Department of Mathematics and Statistics, Maynooth University, Maynooth, Co. Kildare Ireland, W23 F2H6.
ACS Appl Mater Interfaces. 2024 Sep 25;16(38):50846-50858. doi: 10.1021/acsami.4c10870. Epub 2024 Sep 12.
The layered double hydroxides (LDHs) have demonstrated significant potential as non-noble-metal electrocatalysts for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Their unique compositional and structural properties contribute to their efficiency and stability as catalysts. In this study, CoCuFe-LDH composites were grown on graphene (G) via a cost-effective and straightforward one-step hydrothermal process. A 2-level full-factorial model was employed to determine the impact of Co (1.5, 3, and 4.5 mmol) and graphene (10, 30, and 50 mg) concentrations on the onset potential of OER and HER, which were the chosen response variables. OER and HER activity variabilities were assessed in triplicate using CoCuFe-LDH/G (central point), which were determined at 0.01% and 0.02%, respectively. Statistical analyses demonstrated that CoCuFe-LDH/G and CoCuFe-LDH/G showed the lowest onset potential at 1.52 V and -0.32 V (V vs RHE) for the OER and HER, respectively, suggesting that a high cobalt concentration enhances OER performance, while optimal HER catalysis was achieved with lower cobalt concentrations. Moreover, the trimetallic composites exhibited good stability with negligible loss of catalytic activity over 24 h.
层状双氢氧化物(LDHs)已显示出作为析氢反应(HER)和析氧反应(OER)的非贵金属电催化剂的巨大潜力。它们独特的组成和结构特性有助于其作为催化剂的效率和稳定性。在本研究中,通过一种经济高效且简单的一步水热法在石墨烯(G)上生长了CoCuFe-LDH复合材料。采用二级全因子模型来确定Co(1.5、3和4.5 mmol)和石墨烯(10、30和50 mg)浓度对OER和HER起始电位的影响,这两个电位是选定的响应变量。使用CoCuFe-LDH/G(中心点)对OER和HER活性变异性进行了三次评估,其分别在0.01%和0.02%的水平下测定。统计分析表明,CoCuFe-LDH/G和CoCuFe-LDH/G分别在1.52 V和-0.32 V(V vs RHE)时对OER和HER显示出最低的起始电位,这表明高钴浓度可提高OER性能,而较低的钴浓度可实现最佳的HER催化效果。此外,三金属复合材料表现出良好的稳定性,在24小时内催化活性损失可忽略不计。