Boron-dipyrromethene (BODIPY) dyes have turned out to be a challenge for many Time-Dependent Density Functional Theory (TD-DFT) methods. Almost all DFT methods overestimate the absorption energies of BODIPY dyes.1 Many rigorous benchmarking studies involving both wavefunction and TD-DFT methods have emerged trying to identify an accurate method for the calculation of their absorption energies.1 Many researchers have also developed non-DFT based strategies to bring accuracy for the calculated numbers.2 However, no one identified solutions within the TD-DFT regime for this overestimation problem. In 2021, the Goerigk group developed a class of spin-scaled double-hybrid functionals exclusively for excited state calculations.3 These spin-scaled double hybrids represent a more advanced version of the existing double hybrids, but they remained untested on BODIPYs. In our first work,4 we carried out a first benchmark study for BODIPY’s absorptions with our spin-scaled double hybrids along with 14 other DFT methods belonging to two highest rungs of the Jacob’s ladder, on a diverse set of BODIPY derivatives.4 Our study showed that most spin-scaled double hybrids give significantly better results, closer to the experimental absorption references without overestimation. Following this initial study, we extended our benchmark study to BODIPY’s emissions and the Stoke shifts.5 Unlike absorptions, BODIPY’s emissions has not been explored in detail in the literature. Thus, our study5 presents the first benchmark study in this area. Challenges arose in acquiring the suitable excited state geometries for BODIPYs. Regardless, the benchmarking emission results and the Stoke shifts were in favor of our spin-scaled double hybrids as in absorptions. This verifies the robustness of the spin-scaled double hybrids for excited state calculations. Therefore, we suggest TD-DFT users to utilize the recommended spin-scaled double hybrids for accurate computational treatment of BODIPY dyes.