Topochemical Synthesis, Anion Exchange, and Exfoliation of Co−Ni Layered Double Hydroxides: A Route to Positively Charged Co−Ni Hydroxide Nanosheets with Tunable Composition

Abstract

This paper describes the topochemical synthesis of Co−Ni layered double hydroxides (LDHs) from brucite-like Co−Ni hydroxides through a novel oxidative intercalation process employing bromine as an oxidizing agent, and their exfoliation into positively charged unilamellar nanosheets in formamide after anion-exchange treatment. In this protocol, hexagonal microplatelets of brucite-like Co−Ni hydroxides in variable composition were prepared by homogeneous precipitation of a mixed solution of divalent cobalt and nickel ions via hexamethylenetetramine hydrolysis. Subsequent treatment of the brucite-like Co−Ni hydroxides with excessive bromine in acetonitrile promoted partial oxidation of Co 2+ into Co 3+, producing Br − -intercalated Co−Ni LDHs inheriting the hexagonal morphology. This rational topochemical approach was applicable for realizing a pure phase of Co−Ni LDHs with nickel content up to 50% (metal content). Chemical analyses indicated that as-prepared Co−Ni−Br LDHs were unexceptionally characterized by a general chemical formula as [(Co 2+ 1−3 x /2 Ni 2+ 3 x /2 ) 2/3 Co 3+ 1/3 (OH − ) 2 ][Br − 1/3 ·0.5H 2 O] ( x ≤ 0.5), a thermodynamically stable LDH structure with a M 2+ /M 3+ ratio of 2:1. We developed an ethanol-assisted anion-exchange approach, which was effective in preventing carbonate contamination in preparing a variety of inorganic and organic anionic forms of Co−Ni LDHs. As-prepared NO 3 − intercalated Co−Ni LDHs without substantial carbonate contamination were successfully exfoliated into unilamellar nanosheets bearing positive charges upon contact with formamide. The translucent nanosheet suspensions exhibited characteristic colors depending on the variable Co/Ni ratio.