Design of well-defined shell-core covalent organic frameworks/metal sulfide as an efficient Z-scheme heterojunction for photocatalytic water splitting.

Development of a covalent-organic framework (COF)-based Z-scheme heterostructure is a promising strategy for solar energy driven water splitting, but the construction of a COF-based Z-scheme heterostructure with well-defined architecture, large contact area and intimate contact interfaces is scarce. Herein, we fabricated a direct Z-scheme heterostructure COF-metal sulfide hybrid (T-COF@CdS) with shell-core architecture by self-polymerization of 1,3,5-benzenetricarboxaldehyde and 2,4,6-tris(4-aminophenyl)-1,3,5-triazine on CdS. The formed C-S chemical bonding between T-COF and CdS could provide a very tight and stable interface.

Inside-mode indium oxide/carbon nanotubes for efficient carbon dioxide electroreduction by suppressing hydrogen evolution.

The hydrogen evolution reaction is a huge challenge for CO2 electroreduction. Herein, an inside-mode indium oxide/carbon nanotube compound (MWCNTs@In2O3) is developed to maximize the catalytic effect and suppress hydrogen evolution, its HCOOH selectivity can reach up to 92.2% at -16.

MOF-Templated Fabrication of Hollow CoN@N-Doped Carbon Porous Nanocages with Superior Catalytic Activity.

Metallic CoN catalysts have been considered as one of the most promising non-noble materials for heterogeneous catalysis because of their high electrical conductivity, great magnetic property, and high intrinsic activity. However, the metastable properties seriously limit their applications for heterogeneous water phase catalysis. In this work, a novel Co-metal-organic framework (MOF)-derived hollow porous nanocages (PNCs) composed of metallic CoN and N-doped carbon (NC) were synthesized for the first time.