State Key Laboratory of Chemical Resource Engineering, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, P.O. Box 98, Beijing 100029, P.R. China.
Nanoscale. 2018 Jul 19;10(28):13555-13564. doi: 10.1039/c8nr04776f.
Currently, designing and developing high-performance, cost-effective yet stable electrocatalysts for oxygen evolution reaction (OER) is a challenging task owing to the existing high overpotential and sluggish OER kinetics. Herein, we successfully fabricated a hierarchical necklace-like nanohybrid via assembling Ni-Co mixed metal phosphides/carbon (NiCoP/C) hollow nanocages and nanosheets with carbon nanotubes (CNTs). It was revealed that Ni-Co-layered double hydroxide/carbon hollow nanocages and nanosheets derived from Co-based MOF polyhedrons (ZIF-67) could pass through CNTs and perpendicularly anchor onto the surface of CNTs, respectively, thus finally constructing a hierarchical CNTs@NiCoP/C nanohybrid via further low-temperature phosphorization. The as-assembled CNTs@NiCoP/C electrocatalyst exhibited promising electrocatalytic performance towards OER with a low overpotential of about 0.297 V for reaching a current density of 10.0 mA cm-2 and a low Tafel slope of 57.35 mV dec-1 in 1.0 M KOH owing to the advantages of its unique superstructure and multiple composition. Furthermore, the present CNTs@NiCoP/C also possessed good long-term operation stability. This synthesis strategy involving the combination of transition metal phosphides and CNTs to form hierarchical nanostructures holds promising potential for designing highly OER-active electrocatalysts.
目前,由于存在高过电位和缓慢的 OER 动力学,设计和开发用于氧析出反应 (OER) 的高性能、具有成本效益且稳定的电催化剂是一项具有挑战性的任务。在此,我们通过组装 Ni-Co 混合金属磷化物/碳 (NiCoP/C) 空心纳米笼和纳米片与碳纳米管 (CNTs),成功制备了一种分级项链状纳米杂化物。结果表明,源自 Co 基 MOF 多面体 (ZIF-67) 的 Ni-Co 层状双氢氧化物/碳空心纳米笼和纳米片可以穿过 CNTs 并分别垂直锚定在 CNTs 的表面上,从而最终通过进一步的低温磷化构建了分级 CNTs@NiCoP/C 纳米杂化物。所组装的 CNTs@NiCoP/C 电催化剂在 1.0 M KOH 中表现出有前途的 OER 电催化性能,其达到 10.0 mA cm-2 的电流密度的过电位约为 0.297 V,Tafel 斜率低至 57.35 mV dec-1,这得益于其独特的超结构和多种组成的优势。此外,目前的 CNTs@NiCoP/C 还具有良好的长期运行稳定性。这种涉及将过渡金属磷化物与 CNTs 结合形成分级纳米结构的合成策略在设计高 OER 活性电催化剂方面具有很大的潜力。