Karpuraranjith Marimuthu, Chen Yuanfu, Wang Bin, Ramkumar Jeyagopal, Yang Dongxu, Srinivas Katam, Wang Wei, Zhang Wanli, Manigandan Ramadoss
School of Electronic Science and Technology, and State Key Laboratory of Electronic Thin Films and Integrated Devices, University of Electronic Science and Technology of China, Chengdu 610054, PR China.
School of Electronic Science and Technology, and State Key Laboratory of Electronic Thin Films and Integrated Devices, University of Electronic Science and Technology of China, Chengdu 610054, PR China; School of Science and Institute of Oxygen Supply, Tibet University, Lhasa 850000, PR China.
J Colloid Interface Sci. 2021 Jun 15;592:385-396. doi: 10.1016/j.jcis.2021.02.062. Epub 2021 Feb 23.
Rational design and highly efficient dual-functional catalyst are still difficult to develop for electrocatalytic oxygen evolution reaction and degradation of RhB dye pollutant. Herein, we report a highly efficient "bandgap matching and interfacial coupling" strategy to synthesize nano-assembled ultrathin layered MoS@NiFeO (MS@NiFeO) bifunctional catalyst constructed by the hydrothermal route and subsequently amine-hydrolysis. The OER performance of the prepared MS@NiFeO catalyst delivers a low overpotential of 290 mV at 10 mA/cm and Tafel slope is 69.2 mV dec in an alkaline solution. In addition, the nano-assembled ultrathin layered structure of MS@NiFeO showed a highly efficient (96.37%) RhB dye degradation performance than that of MoS nanosheets and NiFeO nanostructures. Unique nanostructure of ultrathin layered MS@NiFeO with suitable band matching, interfacial charge transfer, high surface area and more active sites favored for the enhancement of the catalytic activity. This work presents an unpretentious construction and low-cost production strategy to synthesize bifunctional hybrid catalyst for oxygen evolution reaction as well as degradation of organic pollutant with superior efficiency and longer stability.
对于电催化析氧反应和降解罗丹明B染料污染物而言,合理设计和高效的双功能催化剂仍然难以开发。在此,我们报道了一种高效的“带隙匹配和界面耦合”策略,通过水热法和随后的胺水解合成纳米组装超薄层状MoS@NiFeO(MS@NiFeO)双功能催化剂。制备的MS@NiFeO催化剂在碱性溶液中于10 mA/cm²时的析氧反应性能具有290 mV的低过电位,塔菲尔斜率为69.2 mV/dec。此外,MS@NiFeO的纳米组装超薄层状结构显示出比MoS纳米片和NiFeO纳米结构更高的(96.37%)罗丹明B染料降解性能。具有合适能带匹配、界面电荷转移、高表面积和更多活性位点的超薄层状MS@NiFeO独特纳米结构有利于提高催化活性。这项工作提出了一种简单的构建和低成本生产策略,以合成用于析氧反应以及高效降解有机污染物且具有更长稳定性的双功能混合催化剂。