材料科学
成核
氢氧化物
化学工程
纳米线
析氧
异质结
多孔性
塔菲尔方程
分解水
纳米技术
催化作用
电极
光电子学
电化学
复合材料
物理化学
化学
有机化学
工程类
生物化学
光催化
作者
Ying Wang,Liting Yan,Kamran Dastafkan,Chuan Zhao,Xuebo Zhao,Yingying Xue,Jiamin Huo,Shu-Ni Li,Quan‐Guo Zhai
标识
DOI:10.1002/adma.202006351
摘要
The conjugation of metal-organic frameworks (MOFs) into different multicomponent materials to precisely construct aligned heterostructures is fascinating but elusive owing to the disparate interfacial energy and nucleation kinetics. Herein, a promising lattice-matching growth strategy is demonstrated for conductive MOF/layered double hydroxide (cMOF/LDH) heteronanotube arrays with highly ordered hierarchical porous structures enabling an ultraefficient oxygen evolution reaction (OER). CoNiFe-LDH nanowires are used as interior template to engineer an interface by inlaying cMOF and matching two crystal lattice systems, thus conducting a graft growth of cMOF/LDH heterostructures along the LDH nanowire. A class of hierarchical porous cMOF/LDH heteronanotube arrays is produced through continuously regulating the transformation degree. The synergistic effects of the cMOF and LDH components significantly promote the chemical and electronic structures of the heteronanotube arrays and their electroactive surface area. Optimized heteronanotube arrays exhibit extraordinary OER activity with ultralow overpotentials of 216 and 227 mV to deliver current densities of 50 and 100 mA cm-2 with a small Tafel slope of 34.1 mV dec-1 , ranking it among the best MOF and non-noble-metal-based catalysts for OER. The robust performance under high current density and vigorous gas bubble conditions enable such hierarchical MOF/LDH heteronanotube arrays as promising materials for practical water electrolysis.
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