• 文献标题:   Graphene oxide mediated self-sacrificial synthesis of LaCO3OH-Ni(OH)(2)@ graphene hierarchical composite for photocatalytic H-2 evolution and supercapacitor
  • 文献类型:   Article
  • 作  者:   LV T, XU ZN, HONG W, LI GF, LI YW, JIA LS
  • 作者关键词:   laco3oh, hierarchical composite, ni oh 2 @graphene, supercapacitor, photocatalytic
  • 出版物名称:   CHEMICAL ENGINEERING JOURNAL
  • ISSN:   1385-8947 EI 1873-3212
  • 通讯作者地址:   Xiamen Univ
  • 被引频次:   3
  • DOI:   10.1016/j.cej.2019.123021
  • 出版年:   2020

▎ 摘  要

Herein, we designed a one-step lattice-confined etching perovskite nanoparticles and self-sacrificing graphene oxide (GO) induced self-assembly strategy to synthesize novel 3D nest-like LaCO3OH and flower-like Ni(OH)(2)@graphene (RGO) hierarchical composite as a high performance photocatalyst and electrode material. The lattice-confined effect regulates the concentration and distribution of nickel ions migrating from perovskite to GO and thus constructs a homogeneous Ni(OH)(2)@RGO nanostructure. La(OH)(3) formed by residual lattice frames react with CO32- from self-sacrificing of GO self-assembly to form nest-like LaCO3OH, which is embedded in the Ni (OH)(2)@RGO nanosheets. GO was utilized as both morphology control reagent and self-sacrificed carbon source. Benefit from the extremely rapid transfer of electron on the homogeneous Ni(OH)(2)@RGO nanosheets and high light-harvesting capacity of 3D nest and flower-like composite of LaCO3OH-Ni(OH)(2)@RGO, the properties of photocatalysis and supercapacitor are greatly enhanced. The H-2 production rate of 1.3807 mmol h(-1) g(-1) has been achieved which is 13 times higher than pure LaCO3OH. Electrochemical studies showed that a specific capacitance of 572.47 F g(-1) was obtained at a scan rate of 10 mv/s with 80% capacitance retention even after 20,000 cycles. This composite synthesized from GO mediated etching solid phase perovskite surface ion migration under lattice-confined action provides a novel technical route for the direct self-assembly of solid nanoparticles and GO to synthesize new functional materials.