In semiconductors, quantum confinement can greatly enhance the interaction between band carriers (electrons and holes) and dopant atoms. One manifestation of this enhancement is the increased stability of exciton magnetic polarons in magnetically-doped nanostructures. In the limit of very strong 0D confinement that is realized in colloidal semiconductor nanocrystals, a single exciton can exert an effective exchange field Bex on the embedded magnetic dopants that exceeds several tesla. Here we use the very sensitive method of resonant photoluminescence (PL) to directly measure the presence and properties of exciton magnetic polarons in colloidal Cd1−xMnxSe nanocrystals. Despite small Mn 2+ concentrations (x=0.4-1.6%), large polaron binding energies up to ∼26 meV are observed at low temperatures via the substantial Stokes shift between the pump laser and the resonant PL maximum, indicating nearly complete alignment of all Mn 2+ spins by Bex. Temperature and magnetic field-dependent studies reveal that Bex ≈ 10 T in these nanocrystals, in good agreement with theoretical estimates. Further, the emission linewidths provide direct insight into the statistical fluctuations of the Mn 2+ spins. These resonant PL studies provide detailed insight into collective magnetic phenomena, especially in lightly-doped nanocrystals where conventional techniques such as nonresonant PL or time-resolved PL provide ambiguous results.Advances in the colloidal synthesis of magneticallydoped nanomaterials have sparked a renewed focus on low-dimensional magnetic semiconductors [1][2][3][4][5][6][7][8]. The interesting magnetic properties of these materials originates in the strong sp-d exchange interactions that exist between carrier spins (i.e., band electrons and holes with s-and p-type wavefunctions) and the local 3d spins of embedded paramagnetic dopant atoms such as Mn, Co,. At the microscopic level, the strength of this interaction for a dopant located at position r i scales with the probability density of the carrier envelope wavefunctions at that point: |ψ e,h (r i )| 2 . As such, local spin-spin interactions can be greatly enhanced by strong quantum confinement, which compresses carrier wavefunctions to nanometer-scale volumes and therefore increases |ψ e,h (r)| 2 . The extent to which these exchange interactions can be enhanced and controlled via quantum confinement is an area of significant current interest and has recently been studied in a variety of magnetically-doped semiconductor nanostructures, including nanoribbons [12, 13], nanoplatelets [14], epitaxial quantum dots [14][15][16][18][19][20][21][22][23][24][25][26], and colloidal nanocrystals [1-8, 27, 28, 30].A particularly striking consequence of sp-d interactions in II-VI semiconductors is the formation of exciton magnetic polarons (EMPs), wherein the effective magnetic exchange field from a single photogenerated exciton -B ex -induces the collective and spontaneous ferromagnetic alignment of the magnetic dopants within its wavefunction envelope, generating a net local...