Precise microscale patterning is a prerequisite to incorporate the emerging colloidal metal halide perovskite nanocrystals into advanced, integrated optoelectronic platforms for widespread technological applications. Current patterning methods suffer from some combination of limitations in patterning quality, versatility, and compatibility with the workflows of device fabrication. This work introduces the direct optical patterning of perovskite nanocrystals with ligand cross-linkers or DOPPLCER. The underlying, nonspecific cross-linking chemistry involved in DOPPLCER supports high-resolution, multicolored patterning of a broad scope of perovskite nanocrystals with their native ligands. Patterned nanocrystal films show photoluminescence (after postpatterning surface treatment), electroluminescence, and photoconductivity on par with those of conventional nonpatterned films. Prototype, pixelated light-emitting diodes show peak external quantum efficiency of 6.8% and luminance over 20,000 cd m −2 . Both are among the highest for patterned perovskite nanocrystal devices. These results create new possibilities in the system-level integration of perovskite nanomaterials and advance their applications in various optoelectronic and photonic platforms.

A N2 fixation by the electrocatalytic nitrogen reduction reaction from humidified air is regarded to be a critical tool for producing NH3 and reducing the globally accelerating CO2 emissions. Notwithstanding great efforts to improve catalyst activity and selectivity, promoting catalyst accessibility to high N2 concentrations to ensure that active sites fulfill their function should be a promising design direction. Here, Au nanoparticles are firmly anchored through atomic O on the surface of two-dimensional Ti3C2 using an ultrasound reduction process. Akin to the conspicuous role of the web in the predatory process of spiders, N2 adsorption experiments primarily suggest that a Ti3C2 “web” is beneficial for extraction of N2 from air, and embedding high valence-state Au clusters in the Ti3C2 “web” strengthens the chemical bonding effect toward N2 molecules. The high energy of N2 adsorption on the interface between gold clusters and Ti3C2 is the driving force for weakening triple NN bonds, and thereby the activation energy barrier is lowered via effective stabilization of N2H* species and destabilizing NH2NH2* under an alternative pathway. With Au loading content of ∼0.94%, Au/Ti3C2 exhibits an outstanding average yield of 30.06 μg h–1 mg–1 for NH3 production, with a high Faraday efficiency of 18.34% at −0.2 V.