Spontaneous synthesis of silver nanoparticles on cobalt-molybdenum layer double hydroxide nanocages for improved oxygen evolution reaction

Abstract

Modulating electronic resistance properties and enhancing both active site populations and per-site activity are highly desirable for the application of layered double hydroxides (LDHs) in the electrocatalytic oxygen evolution reaction (OER). Herein, a metal-support structure consisting of silver (Ag) nanoparticles supported by MoO42− intercalated Co-LDH (CoMo-LDH) nanocages (Ag@CoMo-LDH) was developed using a sacrificial template method and a subsequent spontaneous strategy. The resultant hybrid was shown to be a highly efficient OER electrocatalyst in alkaline media. The required overpotential of Ag@CoMo-LDH for affording a geometric current density of 10 mA cm−2 is as low as 205 mV, which is not only significantly lower than that of separate CoMo-LDH or Ag nanoparticles but also superior to that of most developed OER electrocatalysts reported recently. The constituents and respective work mechanism of Ag@CoMo-LDH are discussed in detail. The superior performance of Ag@CoMo-LDH is related to the unique construction and the effective and stable heterointerfaces between Ag nanoparticles and CoMo-LDH, which accelerate the electron and mass transfer, provide a large number of new active sites and optimize the activity of the original sites. Impressively, Ag@CoMo-LDH also exhibited promising practical prospect on account of the remarkable cyclic and long-term stability. This finding demonstrates that pointedly integrating multiple strategies into one system is a promising way to construct new LDH-based OER electrocatalysts with synthetically improved performance, providing a promising model for developing advanced electrocatalysts in energy conversion devices.