the visible to near-IR wavelengths of the electromagnetic spectrum. [9,10] Though organic-inorganic metal halides based perovskites can produce high photoluminescence (PL) yield, their instability makes it difficult for practical use. On the other side, all inorganic perovskite, e.g., cesium lead halides (CsPbX 3 ), based colloidal quantum dots attract much attention due to its very high PL yield (PLQY ≈ 90%), [11] narrow emission peak (enhanced color purity), low trap density, and reduced blinking [12] with high stability. Recent studies show ultralow threshold density (≈4.5 µJ cm −2 ) for amplified spontaneous emission (ASE) in CsPbBr 3 nanocrystals (NCs) film. [13,14] In past few years the successful employment of CsPbBr 3 quantum dots as light-emitting diodes, [9] single photon emitter, [15] advanced lasing material, [13] and photodetectors [16] make it necessary to have an in-depth study of different photophysical processes in this material. Some recent studies have been devoted to investigating excitonic recombination processes in this material at ultrafast timescale. [17] To date, most of these studies have been done at room temperature (RT). However, to understand the photoexcited carrier dynamics, temperature-dependent time-resolved PL (TRPL) study is an essential tool. Since PL lifetime can be significantly affected by the presence of surface traps, temperature-dependent TRPL gives us an insight of the trap-related kinetics in the NC. [18] Some recent studies [19,20] of the fine structure analysis of the excitonic and PL spectra of CsPbX 3 (X = Cl, Br, I) NCs show the presence of trion formation at low T. These trions are red-shifted by few meV from free excitons peak and decay radiatively with much faster rate than the excitons which results in faster PL decay at low T. [19,21] It has also been argued that the lowest triplet excitonic states are bright (emission red-shifted by few meV) in this material which is the cause of the higher photon emission rate. [22] Here, we have studied temperature-dependent TRPL decay of CsPbBr 3 NCs along with the steady-state absorption and PL to get insight into the influence of surface trap states on the emission kinetics in highly luminescent NCs. From timeresolved emission spectroscopy, we have found that the PL decaying faster at low temperature is in contrast to many other colloidal NCs such as PbS and CdS, [23,24] where PL lifetime gets extended by lowering the temperature. However, similar lengthening of PL lifetimes at elevated temperatures has also Temperature-dependent time-resolved photoluminescence (TRPL) spectroscopy of high optical gain CsPbBr 3 nanocrystals (NCs) films along with temperaturedependent steady-state absorption and photoluminescence (PL) spectra is studied. A red shift in the optical band edge and the corresponding PL peak is observed by lowering the temperature from room temperature, analogous to hybrid perovskite semiconductors. However, the faster PL decay of CsPbBr 3 NCs film at a low temperature as compared to room temperature is in con...