No abstract

Solar‐driven photocatalytic CO2 reduction is regarded as a promising way to simultaneously mitigate the energy crisis and CO2 pollution. However, achieving high efficiency of photocatalytic CO2 reduction, especially without the assistance of sacrifice reagents or extra alkaline additives, remains a critical issue. Herein, a photocatalyst of 3D ordered macroporous N‐doped carbon (NC) supported CdS quantum dots (3DOM CdSQD/NC) is successfully fabricated toward photocatalytic CO2 reduction via an in situ transformation strategy. Additionally, an amines oxidation reaction is introduced to replace the H2O oxidation process to further boost the photocatalytic CO2 reduction efficiency. Impressively, 3DOM CdSQD/NC exhibits superior activity and selectivity in photocatalytic CO2 reduction coupled with amines oxidation, affording a CO production rate as high as 5210 µmol g−1 h−1 in the absence of any sacrificial agents and alkaline additives. Moreover, 3DOM CdSQD/NC achieves an apparent quantum efficiency of 2.9% at 450 nm. Mechanism studies indicate that the 3D ordered macropores in the NC matrix are beneficial to the transfer of photogenerated carriers. Furthermore, the highly dispersed CdS QDs on the NC skeleton are able to significantly promote the adsorption of both CO2 and amine molecules and depress the CO2 activation energy barriers by stabilizing the *COOH intermediate, directly contributing to the high activity.

This review narrates the recent developments on the catalytic applications of pristine metal–organic frameworks (MOFs), functionalized MOFs, guests embedded over MOFs and MOFs derived carbon composites for biomass conversion into platform chemicals.

Rationally tailoring the coordination environments of metal single atoms (SAs) is an effective approach to promote their catalytic performances, which, however, remains as a challenge to date. Here, we report a novel misplaced deposition strategy for the fabrication of differently coordinated dual-metal hetero-SAs. Systematic characterization results imply that the as-synthesized dual-metal hetero-SAs (exemplified by Cu and Co) are affixed to a hierarchical carbon support via Cu–C4 and Co–N4 coordination bonds. Density functional theory studies reveal that the strong synergistic interactions between the asymmetrically deployed CuC4 and CoN4 sites lead to remarkably polarized charge distributions, i.e., electron accumulation and deficiency around CuC4 and CoN4 sites, respectively. The obtained CuC4/CoN4@HC catalyst exhibits significantly enhanced capability in substrate adsorption and O2 activation, achieving superior catalytic performances in the oxidative esterification of aromatic aldehydes in comparison with the Cu- and Co-based SA counterparts.

A new one-dimensional hierarchical hollow MnO2 nanotubes@NiCo-LDH/CoS2 nanocage supercapacitor, MnO2@NiCo-LDH/CoS2, achieves a high specific capacitance and high stability.