Xu Hanwen, Zhang Wen-Da, Liu Jiangyong, Yao Yang, Yan Xiaodong, Gu Zhi-Guo
Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, China.
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China.
J Colloid Interface Sci. 2022 Feb;607(Pt 2):1353-1361. doi: 10.1016/j.jcis.2021.09.105. Epub 2021 Sep 22.
Edge sites and interlayer space of NiFe layered double hydroxides (LDHs) play an important role in water oxidation. However, the combined effect of interlayer expansion and partial exfoliation on the catalytic activity is yet to be investigated. Herein, scalable synthesis of partially exfoliated citrate-intercalated NiFe LDHs with tunable interlayer space have been achieved. The effect of citrate concentration on the phase, morphology, surface elemental composition, electronic states of surface metals, and electrochemical properties are comprehensively studied. The unique structure results in improved intrinsic catalytic activity and abundant active edge sites for oxygen evolution reaction. The optimal NiFe LDHs show an overpotential of 225 mV at 10 mA cm, which is much smaller than that (∼305 mV) of the single-layer NiFe LDH nanosheets reported in the literature. The high catalytic activity can be mainly attributed to the combined effect between the enlarged interlayer space and the partial exfoliation/nanosheet thickness. That is, the interlayer space is related to the reaction kinetics/mechanism, while the degree of exfoliation affects the magnitude of the current density at a certain potential.
镍铁层状双氢氧化物(LDHs)的边缘位点和层间空间在水氧化过程中起着重要作用。然而,层间膨胀和部分剥离对催化活性的综合影响尚未得到研究。在此,已实现了具有可调层间空间的部分剥离的柠檬酸盐插层镍铁LDHs的可扩展合成。全面研究了柠檬酸盐浓度对相、形态、表面元素组成、表面金属的电子态以及电化学性质的影响。独特的结构导致本征催化活性提高以及析氧反应有丰富的活性边缘位点。最优的镍铁LDHs在10 mA cm时的过电位为225 mV,远小于文献报道的单层镍铁LDH纳米片的过电位(约305 mV)。高催化活性主要可归因于层间空间扩大与部分剥离/纳米片厚度之间的综合作用。也就是说,层间空间与反应动力学/机理相关,而剥离程度在一定电位下影响电流密度的大小。