Near-IR Electrochromism in Electrodeposited Thin Films of Cyclometalated Complexes

ACS Appl Mater Interfaces. 2016 May 18;8(19):12272-81. doi: 10.1021/acsami.6b01167. Epub 2016 May 4.

Abstract

Homogeneous thin films of controlled thickness obtained from cyclometalated complexes of general formula [(C(∧)N)M(O(∧)N)], where M = Pd(II) or Pt(II), H(C(∧)N) = 2-phenylpyridine and, respectively, 2-thienylpyridine and H(O(∧)N) = a triphenylamine functionalized Schiff base, have been deposited by oxidative electropolymerization. The films have been electrochemically and morphologically characterized. The metallopolymeric thin films present stable reversible redox behavior and typical cauliflower-like textures in agreement with a nucleation-growth electropolymerization mechanism. However, the film growth is greatly influenced by the nature of the metal center, with a higher tendency of the Pt complexes to promote the 3D growth. Furthermore, a complete spectroelectrochemical study has been performed on electrodeposited films showing near-IR absorption in the oxidized state, high contrast ratios (up to 65%) and low response times.

Keywords: Pd(II) complexes; Pt(II) complexes; Pt—Pt interactions; cyclometalated metallopolymers; electropolymerization and electrochromism.

Publication types

  • Research Support, Non-U.S. Gov't