and thus abundant PL emissions covering ultraviolet, visible light, as well as infrared region. [11,12] In addition, the FWHM could even reach 10 nm, enabling high color purity and serving as phosphors in display, biolabeling, etc. [13,14] Recently, some reports demonstrated that colloidal CsPbX 3 NCs with Mn 2+ doping exhibited dual-color emission, validating the facile doping in perovskites due to their nonrigid structures. [15][16][17] Manganese (Mn) ions were incorporated into CsPbX 3 NCs, exhibiting a dramatic effect on relative intensities of intrinsic band-edge emission and Mn ion emission, which was ascribed to the influence of energy transfer between the Mn ion and the semiconductor host. Subsequently, Sn 2+ , Cd 2+ , and Zn 2+ are found to partially replace Pb 2+ cations in colloidal CsPbBr 3 NCs by the method of cation exchange and lead to a blueshift of the optical spectra, while maintaining the high photoluminescence quantum yields (>50%) and narrow emission of the parent NCs. [18] However, as far as we are concerned, there is still no report about RE ion doping in lead halide perovskite NCs.In the present work, we successfully doped the RE ions Eu 3+ and Tb 3+ into CsPbBr 3 NCs through one-pot ultrasonication. The ultrasonic method has been proven a successful route for nanocrystal synthesis. [19][20][21] During the ultrasonication, acoustic cavitation could create bubbles, with the temperature of hot spots reaching above 5000 K and the pressure exceeding 1000 bar, and hence accumulate intensive energy inside. [22] Collapse of these bubbles supplies a transient ultrahigh energy to overcome the nucleation barrier and initiates the growth of NCs simultaneously. [23] Here, we believe that the ultrasonication could not only provide energy for the synthesis of our CsPbBr 3 NCs, but also facilitate the incorporation of RE dopants into the NC lattices. We thus developed a one-pot strategy to synthesize RE ion-doped halide perovskite NCs, and the synthetic process is schematically shown in Figure 1. Briefly, CsBr and PbBr 2 powder was loaded into N,N-Dimethylformamide (DMF) solution containing a proper amount of RE ions, and then the solution was subjected to ultrasonication with the assistance of water cooling. RE ion-doped CsPbBr 3 NCs were collected after centrifugation and other processes. The detailed procedure was documented in the Experimental Section. Such method has a relatively low yield (around 4.32%), and we can always find the undissolved precursors (CsBr, PbBr 2 ) in the bottom. These undissolved precursors can be reused for another sonication cycle to enable high utilization efficiency.The products were first characterized by transmission electron microscope (TEM) images, as shown in Figure 2a-c. The nondoped and doped NCs exhibited cubic shapes with different levels of aggregate and slight truncations caused by the ultrasonication synthesis procedure. The average sizes of CsPbBr 3 , CsPbBr 3 :Eu 3+ ,