Abstract
The construction of heterogeneous frustrated Lewis pairs (FLPs) with performance comparable to or surpassing the homogeneous counterparts in H2activation is a long-standing challenge. Herein, sterically hindered Lewis acid ("B" center) and Lewis base ("N" center) sites were anchored within the rigid lattice of highly crystalline hexagonal boron nitride (h-BN) scaffolds. The active sites were created via precision defect regulation during the molten-salt-involved (NaNH2and NaBH4) h-BN construction procedure. The as-afforded h-BN scaffolds achieved highly efficient H2/D2activation and dissociation under ambient pressure via FLP-like behavior, and attractive catalytic efficiency in hydrogenation reactions surpassing the current heterogeneous analogues.
Original language | English |
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Pages (from-to) | 10688-10693 |
Number of pages | 6 |
Journal | Journal of the American Chemical Society |
Volume | 144 |
Issue number | 24 |
DOIs | |
State | Published - Jun 22 2022 |
Funding
The research was supported financially by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division, Catalysis Science program. The IR study was conducted as part of a user project at the Center for Nanophase Materials Sciences, which is a US Department of Energy, Office of Science User Facility at Oak Ridge National Laboratory. J. F was supported by the National Natural Science Foundation of China (No. 22022812, 21978259) and the Fundamental Research Funds for the Central Universities.