Quantum dots (QDs) are a particularly interesting nanostructure for applications that require optical emission in the visible or near-infrared spectrum. These small (D < 10 nm) semiconducting nanoparticles exhibit size-dependent broadband absorption and narrowband photoluminescence (PL) (full-width half-maximum (FWHM) below 40 nm) due to quantum confinement of the exciton. [9][10][11] Many synthesis approaches have been developed for different QD architectures, including core, [12] core-shell, [13,14] alloyed coreshell, [15] and even core-shell-shell QDs, [16] which offer a range of optical characteristics. Not surprisingly, the intrinsic properties of QDs and the wide variety of QDs available have led to their implementation in a number of applications, including imaging/labeling/sensing in biological investigations, [17] light-emitting diodes (LEDs), [18] solar cells, [19,20] quantum computing, [21] and, more recently, lasers and optical gain media. [22][23][24] In addition, the application of nanotechnology for controlled light-matter interactions has been augmented by the variety of micro-and nanoscale patterning approaches that have been developed, including techniques like electron-and photolithography, [25] soft lithographies, [26,27] inkjet printing, [28] and molding and printing. [29] One of the unifying principles of these approaches is that patterns are created by adding, removing, or rearranging material during a multi-step fabrication procedure. Less investigation has been done on "nonphysical" patterning approaches like spectral photo patterning, which creates patterns by modifying the emission efficiency of quantum dots in specific areas of the film without physically modifying the film. [30][31][32][33] The modification of QD emission efficiency is due to intrinsic modification of the exciton relaxation pathways within the QD, so no physical deposition or removal of material is required to impart an emission pattern in a spectral photopattern. The non-physical aspect of spectral photopatterning is in sharp contrast to the traditional microand nanoscale physical patterning techniques. For this reason, spectral photopatterning could be very useful in areas such as photonic parity-time systems that require periodic modulation of optical gain and loss with no corresponding change in Positive and negative photoluminescent photopattern contrasts arising from intrinsic modification of quantum dot (QD) emission (decay or recovery) upon exposure to light are reported. The ability to fabricate a variety of photopattern types using a single type of quantum dot is due to a two-step decayto-recovery evolution upon light exposure. It is shown that high-contrast photopatterns spanning mm 2 areas can be fabricated within seconds with a facile one-step process, representing a drastic reduction in the time required to develop an emissive pattern in a QD-polymer film (from hours to seconds). Furthermore, the controlled light exposure allows for a programmed transformation of the emissive pattern contrast, with a rev...