Bright and stable blue emitters with narrow full‐width at half‐maxima are particularly desirable for applications in television displays and related technologies. Here, this study shows that doping aluminum (Al³⁺) ion into CsPbBr₃ nanocrystals (NCs) using AlBr₃ can afford lead‐halide perovskites NCs with stable blue photoluminescence. First, theoretical and experimental analyses reveal that the extended band gap and quantum confinement effect of elongated shape give rise to the desirable blueshifted emission. Second, the aluminum ion incorporation path is rationalized qualitatively by invoking fundamental considerations about binding relations in AlBr₃ and its dimer. Finally, the absence of anion‐exchange effect is corroborated when green CsPbBr₃ and blue Al:CsPbBr₃ NCs are mixed. Combinations of the above two NCs with red‐emitting CdSe@ZnS NCs result in UV‐pumped white light‐emitting diodes (LED) with an National Television System Committee (NTSC) value of 116% and ITU‐R Recommendation B.T. 2020 (Rec. 2020) of 87%. The color coordinates of the white LED are optimized at (0.32, 0.34) in CIE 1931. The results suggest that low‐cost, earth‐abundant, solution‐processable Al‐doped perovskite NCs can be promising candidate materials for blue down‐conversion layer in backlit displays.

A new method of fabricating small metal-molecule-metal junctions is developed, approaching the single-molecule limit. The conductance of different conjugated molecules in a broad temperature, source-drain, and gate voltage regime is reported. At low temperature, all investigated molecules display sharp conductance steps periodic in source-drain voltage. The position of these steps can be controlled by a gate potential. The spacing corresponds to the energy of the lowest molecular vibrations. These results show that the low-bias conductance of molecules is dominated by resonant tunneling through coupled electronic and vibration levels.