Construction of Boron‐ and Nitrogen‐Enriched Nanoporous π‐Conjugated Networks Towards Enhanced Hydrogen Activation

Author:

Li Meijia1ORCID,Qiu Liqi2,Popovs Ilja1,Yang Weiwei1,Ivanov Alexander S.1,Kobayashi Takeshi3,Thapaliya Bishnu P.1,Moitra Debabrata2,Yu Xinbin1,Wu Zili14,Yang Zhenzhen1ORCID,Dai Sheng12

Affiliation:

1. Chemical Sciences Division Oak Ridge National Laboratory Oak Ridge TN 37831 USA

2. Department of Chemistry Institute for Advanced Materials and Manufacturing University of Tennessee Knoxville TN 37996 USA

3. U.S. DoE Ames Laboratory Iowa State University Ames IA 50011 USA

4. Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge TN 37831 USA

Abstract

AbstractBoron‐enriched scaffolds have demonstrated unique features and promising performance in the field of catalysis towards the activation of small gas molecules. However, there is still a lack of facile approaches capable of achieving high B doping and abundant porous channels in the targeted catalysts. Herein, construction of boron‐ and nitrogen‐enriched nanoporous π‐conjugated networks (BN‐NCNs) was achieved via a facile ionothermal polymerization procedure with hexaazatriphenylenehexacarbonitrile [HAT(CN)6] sodium borohydride as the starting materials. The as‐produced BN‐NCN scaffolds were featured by high heteroatoms doping (B up to 23 wt. % and N: up to 17 wt. %) and permanent porosity (surface area up to 759 m2 g−1 mainly contributed by micropores). With the unsaturated bonded B species acting as the active Lewis acid sites and defected N species acting as the active Lewis base sites, those BN‐NCNs delivered attractive catalytic performance towards H2 activation/dissociation in both gaseous and liquid phase, acting as efficient metal‐free heterogeneous frustrated Lewis pairs (FLPs) catalysts in hydrogenation procedures.

Funder

Basic Energy Sciences

U.S. Department of Energy

Publisher

Wiley

Subject

General Medicine

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