Recently, there are significant progresses in the growth of organic-inorganic lead halide perovskite single crystals, however, due to their susceptible nucleation and growth mechanisms and solvent requirements, the efficient and generalized growth for these single crystals is still challenging. Here we report the work towards this target with a polymer-controlled nucleation process for the highly efficient growth of large-size high-quality simple ternary, mixed-cations and mixed-halide perovskite single crystals. Among them, the carrier lifetime of FAPbBr3 single crystals is largely improved to 10199 ns. Mixed MA/FAPbBr3 single crystals are synthesized. The crucial point in this process is suggested to be an appropriate coordinative interaction between polymer oxygen groups and Pb2+, greatly decreasing the nuclei concentrations by as much as 4 orders of magnitudes. This polymer-controlled route would help optimizing the solution-based OIHPs crystal growth and promoting applications of perovskite single crystals.

The photocatalytic CO2 reduction reaction is a sustainable route to the direct conversion of greenhouse gases into chemicals without additional energy consumption. Given the vast amount of greenhouse gas, numerous efforts have been devoted to developing inorganic photocatalysts, e.g., titanium dioxide (TiO2), due to their stability, low cost, and environmentally friendly properties. However, a more efficient TiO2 photocatalyst without noble metals is highly desirable for CO2 reduction, and it is both difficult and urgent to produce selectively valuable compounds. Here, a novel “single‐atom site at the atomic step” strategy is developed by anchoring a single tungsten (W) atom site with oxygen‐coordination at the intrinsic steps of classic TiO2 nanoparticles. The composition of active sites for CO2 reduction can be controlled by tuning the additional W5+ to form W5+–O–Ti3+ sites, resulting in both significant CO2 reduction efficiency with 60.6 μmol g−1 h−1 and selectivity for methane (CH4) over carbon monoxide (CO), which exceeds those of pristine TiO2 by more than one order of magnitude. The mechanism relies on the accurate control of the single‐atom sites at step with 22.8% coverage of surface sites and the subsequent excellent electron–hole separation along with the favorable adsorption–desorption of intermediates at the sites.

Galvanic replacement is a versatile approach to prepare hollow nanostructures with controllable morphology and elemental composition. The primary issue is to identify its fundamental mechanism. In this study, in situ liquid cell transmission electron microscopy was employed to monitor the dynamic reaction process and to explore the mechanism of galvanic replacement. The detailed reaction process was revealed based on in situ experiments in which small Au particles first appeared around Ag nanowires; they coalesced, grew, and adhered to Ag nanowires. After that, small pits grew from the edge of Ag nanowires to form tubular structures, and then extended along the Ag nanowires to obtain hollowed structures. All of our experimental observations from the viewpoint of electron microscopy, combined with DFT calculations, contribute towards an in‐depth understanding of the galvanic replacement reaction process and the design of new materials with hollow structures.

Solar thermal water evaporation is a clean, sustainable, and energy-saving approach to fresh water generation compared with traditional methods.

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