An active and stable photocatalyst to directly split water is desirable for solar-energy conversion. However, it is difficult to accomplish overall water splitting without sacrificial electron donors. Herein, we demonstrate a strategy via constructing a single site to simultaneously promote charge separation and catalytic activity for robust overall water splitting. A single Co -P site confined on g-C N nanosheets was prepared by a facile phosphidation method, and identified by electron microscopy and X-ray absorption spectroscopy. This coordinatively unsaturated Co site can effectively suppress charge recombination and prolong carrier lifetime by about 20 times relative to pristine g-C N , and boost water molecular adsorption and activation for oxygen evolution. This single-site photocatalyst exhibits steady and high water splitting activity with H evolution rate up to 410.3 μmol h g , and quantum efficiency as high as 2.2 % at 500 nm.

A NiS/C3 N4 photocatalyst containing earth-abundant elements only was constructed by means of a simple hydrothermal method. This photocatalyst shows efficient hydrogen evolution (48.2 μmol h(-1) ) under visible light when using triethanolamine as a sacrificial reagent. The optimal loading of 1.1 wt % NiS on C3 N4 as a cocatalyst can enhance the H2 production by about 250 times compared with the native C3 N4 . The highest apparent quantum efficiency of 1.9 % was recorded at 440 nm.

A convenient, multigram-scale synthesis of arylene ethynylene macrocycles near room temperature is described. Driven by the precipitation of a diarylacetylene byproduct, alkyne metathesis produces the desired macrocycles in one step from monomers in high yields.

Carbon capture in an organic cage: A shape‐persistent, organic prismatic molecular cage (see structure) was synthesized in one step and high yield from readily accessible starting materials through dynamic covalent chemistry. The resulting cage molecule exhibited high selectivity for the adsorption of CO2 over N2 and thus shows promise as a carbon‐capture material.