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Supported bimetallic AuCu@CeO2 nanocomposites with high Cu-content demonstrate high catalytic activity, selectivity and stability for photocatalytic oxidation of benzyl alcohol.

As an excellent n-type semiconductor, indium oxide (In O ) is also a good candidate for photocatalysis such as light-induced water splitting. However, the efficiency of the oxygen evolution reaction (OER) underperforms in view of the wide band gap (BG) and fast charge recombination in In O . N-doping provides a sound method to narrow the BG and to prohibit the charge recombination by forming new energy levels between the valence band (VB) and the conduction band (CB). In this work, an In-based organic framework sod-ZMOF was used as a precursor to prepare the N-doped In O . After calcination, sod-ZMOF is transformed into N-doped In O nanocrystalline, in which the ligand within sod-ZMOF serves as the nitrogen source. In addition, sod-ZMOF acts as self-template during calcination to generate abundant nanopores within the In O frameworks, providing large specific surface area and active sites for OER. The BG is narrowed to 2.9 from 3.7 eV of the pure In O on account of the N-doping. N species are doped in both the substitutional and interstitial fashion, and the interstitial doping is believed to improve the photo-induced carrier separation by the formation of oxygen vacancies. As a consequence, the overpotential for OER is effectively decreased from the pure In O , and the electrocatalytic experiment proves superior catalytic activity with a high current density and long-term durability compared to the In O nanoparticles obtained from In(OH) .

A novel one-dimensional covalent organic framework (COF-K) was firstly designed and synthesized through a Schiff-based reaction from a porphyrin building block and a nonlinear right-angle building block. The COF-K exhibited high BET surface area and narrow pore size of 1.25 nm and gave a CO2 adsorption capacity of 89 mg g−1 at 273K and 1bar.

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