Nickel@Siloxene catalytic nanosheets for high-performance CO2 methanation

Xiaoliang Yan(University of Toronto), Wei Sun(University of Toronto), Liming Fan(Taiyuan University of Technology), Paul N. Duchesne(University of Toronto), Wu Wang(Karlsruhe Institute of Technology), Christian Kübel(Karlsruhe Institute of Technology), Di Wang(Karlsruhe Institute of Technology), Sai Govind Hari Kumar(University of Toronto), Young Feng Li(University of Toronto), Alexandra Tavasoli(University of Toronto), Thomas E. Wood(University of Toronto), Darius L. H. Hung(University of Toronto), Lili Wan(University of Toronto), Lu Wang(University of Toronto), Rui Song(University of Toronto), Jiuli Guo(University of Toronto), Ilya Gourevich(University of Toronto), Feysal M. Ali(University of Toronto), Jingjun Lu(Taiyuan University of Technology), Ruifeng Li(Taiyuan University of Technology), Benjamin D. Hatton(University of Toronto), Geoffrey A. Ozin(University of Toronto)
Nature Communications
June 13, 2019
Cited by 187Open Access
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Abstract

Abstract Two-dimensional (2D) materials are of considerable interest for catalyzing the heterogeneous conversion of CO 2 to synthetic fuels. In this regard, 2D siloxene nanosheets, have escaped thorough exploration, despite being composed of earth-abundant elements. Herein we demonstrate the remarkable catalytic activity, selectivity, and stability of a nickel@siloxene nanocomposite; it is found that this promising catalytic performance is highly sensitive to the location of the nickel component, being on either the interior or the exterior of adjacent siloxene nanosheets. Control over the location of nickel is achieved by employing the terminal groups of siloxene and varying the solvent used during its nucleation and growth, which ultimately determines the distinct reaction intermediates and pathways for the catalytic CO 2 methanation. Significantly, a CO 2 methanation rate of 100 mmol g Ni −1 h −1 is achieved with over 90% selectivity when nickel resides specifically between the sheets of siloxene.


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