Jafari Sahar, Shaghaghi Zohreh
Coordination Chemistry Research Laboratory, Department of Chemistry, Faculty of Science, Azarbaijan Shahid Madani University, Tabriz, 5375171379, Iran.
Sci Rep. 2025 Feb 3;15(1):4145. doi: 10.1038/s41598-025-87423-8.
The rational design of highly efficient and stable bifunctional catalysts for overall water splitting is vitally important. In this study, to increase the active catalytic sites of CeO for electrochemical water splitting, a ternary CeO-CuO-MnO heterostructure, synthesized by coprecipitation method, is loaded on reduced graphene oxide (rGO) nanosheets in different amounts to produce CeO-CuO-MnO@rGO nanocomposites. It is found that CeO-CuO-MnO@rGO nanocomposites show higher electrocatalytic activity than unsupported samples, and the best activity is observed when the wieght ratio of CeO-CuO-MnO is three times that of rGO. The CeO-CuO-MnO@rGO(3:1) requires low overpotentials of 130 and 270 mV for hydrogen and oxygen evolution reactions (HER and OER) at a current density of 10 mA cm. Furthermore, this material demonstrates a large electrochemically active surface area, low charge transfer resistance, suitable kintics, and high long-term stability for both OER and HER. Additionally, when CeO-CuO-MnO@rGO(3:1) is used as self-supported electrodes for the overall water splitting reaction, a low cell voltage of 1.68 V is obtained. This superior performance is due to: (i) active multi-metal sites that produce strong synergistic effects; (ii) the high conductivity of rGO, which faciliate favorable electron transfer; and (iii) the homogenous anchoring of CeO-CuO-MnO on rGO, which increases the number of active sites available on the catalyst surface.
设计高效稳定的用于全水分解的双功能催化剂至关重要。在本研究中,为增加CeO用于电化学水分解的活性催化位点,通过共沉淀法合成的三元CeO-CuO-MnO异质结构以不同量负载在还原氧化石墨烯(rGO)纳米片上,以制备CeO-CuO-MnO@rGO纳米复合材料。研究发现,CeO-CuO-MnO@rGO纳米复合材料表现出比无载体样品更高的电催化活性,当CeO-CuO-MnO与rGO的重量比为3:1时观察到最佳活性。CeO-CuO-MnO@rGO(3:1)在电流密度为10 mA cm时,析氢反应(HER)和析氧反应(OER)所需的过电位分别低至130和270 mV。此外,该材料具有大的电化学活性表面积、低电荷转移电阻、合适的动力学以及对OER和HER均具有高的长期稳定性。另外,当CeO-CuO-MnO@rGO(3:1)用作全水分解反应的自支撑电极时,可获得1.68 V的低电池电压。这种优异的性能归因于:(i)产生强协同效应的活性多金属位点;(ii)rGO的高导电性,有利于电子的良好转移;(iii)CeO-CuO-MnO在rGO上的均匀锚定,增加了催化剂表面可用的活性位点数量。