Key Laboratory of Macromolecular Science of Shaanxi Province, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an 710062, PR China.
Nanoscale. 2019 Jan 17;11(3):1058-1064. doi: 10.1039/c8nr08104b.
Atomically thick ultrathin nanomeshes (NMs) possessing the inherent advantages of both two-dimensional nanomaterials and porous nanomaterials are attracting increasing interest in catalysis and electrocatalysis. Herein, we report a direct chemical synthesis of atomically thick Ni(OH)2-NMs by a NaBH4 assisted cyanogel hydrolysis method, which overcomes the shortcoming of the post-etching method for NM synthesis. Various physical characterization methods show that the as-synthesized Ni(OH)2-NMs have 1.7 nm thickness, a big surface area, abundant nanoholes, and numerous surface/edge atoms with low-coordination numbers. The as-synthesized Ni(OH)2-NMs show a better electrocatalytic performance for the urea oxidation reaction than conventional Ni(OH)2 nanoparticles without holes in the alkaline electrolyte, including a lower onset oxidation potential, faster reaction kinetics, and higher mass activity.
原子层厚的超薄纳米网(NMs)兼具二维纳米材料和多孔纳米材料的固有优势,在催化和电催化领域引起了越来越多的关注。在此,我们通过 NaBH4 辅助的氰基凝胶水解法报告了原子层厚的 Ni(OH)2-NMs 的直接化学合成,该方法克服了 NM 合成的后蚀刻方法的缺点。各种物理特性表征方法表明,所合成的 Ni(OH)2-NMs 具有 1.7nm 的厚度、大的表面积、丰富的纳米孔和大量表面/边缘原子,这些原子具有低配位数。在碱性电解质中,与没有孔的传统 Ni(OH)2 纳米粒子相比,所合成的 Ni(OH)2-NMs 对尿素氧化反应表现出更好的电催化性能,包括更低的起始氧化电位、更快的反应动力学和更高的质量活性。