Thermal images generated from infrared radiation are useful for monitoring many processes; however, infrared cameras are orders of magnitude more expensive than their visible counterparts. Methods that allow visible cameras to capture thermal images are therefore of interest. In this contribution, thermal images of a surface coated with an inexpensive inorganic micropowder phosphor are generated from the analysis of a video taken with a smartphone camera. The phosphor is designed to have a temperature‐dependent emission lifetime that is long enough to be determined from the analysis of a 30 frames‐per‐second video recording. This proof‐of‐principle work allows temperatures in the 270–320 K range to be accurately determined with a precision better than 2 K, even in the presence of bright background illuminance up to 1500 lm m−2. In the broader context, this inspires further development of phosphors to bring time‐resolved sensing techniques into lifetime long enough ranges to allow smartphone‐based detection.

Dynamic luminescent labels, in which a luminescent image changes with time after ultraviolet excitation is turned off, are attractive for anticounterfeiting. A sequence of Gd2O2S:Eu3+/Ti4+ phosphors is presented in which the Ti4+ doping concentration allows the persistent emission lifetime to be varied from 1.17 ± 0.02 to 5.95 ± 0.07 s. While this persistent lifetime is tuned, the photoluminescence quantum yield remains over 46% ± 3%. A broad charge‐transfer band allows these phosphors to be excited with inexpensive and relatively safe 375 nm light‐emitting diodes. By developing patterns with phosphors that have differing persistent lifetimes, dynamic changes in the luminescent image after the excitation source is removed can be observed. For patterns made from phosphor materials that have big differences in persistent lifetimes, these dynamic changes are observable by the eye. By contrast, the dynamic changes in patterns made by phosphors with comparable persistent lifetimes (0.20 s delayed lifetime difference) are difficult to observe by the naked eye but can be easily determined by analysis of a 30‐frames‐per‐second video taken with a smartphone. Thus, these bright phosphors with tunable persistent lifetime allow both overt (observable by eye) and covert (requiring smartphone video analysis) dynamic anticounterfeiting labels to be created.

Micron‐scale randomness during manufacturing can create unique and unclonable anti‐counterfeiting labels. The security of such labels typically comes at the expense of complex hardware being required for authentication. This work demonstrates unclonable labels that can be authenticated using simple hardware such as a standard light‐emitting diode and smartphone camera. These labels consist of a microlens array laminated to a luminescent‐microparticle‐doped polymer film, and thereby present a new method of making microscopic particle distributions visible on the macroscopic scale. The current novel design offers two significant practical advantages: 1) use of an incoherent source; and 2) authentication independent of the detector position. A comparison of 100 test images against 100 different reference images (total of 10,000 comparisons out of which 100 should authenticate and 9900 should not), demonstrates that authentication is robust with an estimated probability of a false positive on the order of 10−15. Finally, a proof‐of‐concept is demonstrated through successful authentication of a label by a single smartphone, simultaneously providing both excitation and detection on the front side of the label.

A significant impediment to the deployment of anti-counterfeiting technologies is the reliance on specialized hardware. Here, anti-counterfeiting labels are developed that are both excited and detected using a smartphone. The persistent luminescence pattern and color changes on the timescale of hundreds of milliseconds to seconds. The labels can be authenticated by comparing still images from the red and green channels of video acquired at known times after flashlight excitation against expected reference patterns. The labels are based on a green-emitting SrAl2O4: Eu2+,Dy3+ (SAED), and red-emitting CaS:Eu2+ phosphors whose lifetimes are varied: (i) for SAED from 0.5 to 11.7 s by annealing the commercial material in air; and (ii) CaS:Eu2+ from 0.1 to 0.6 s by varying the dopant concentration. Examples of anti-counterfeiting labels exhibiting changing emission patterns and colors on a seven-segment display, barcode, and emoji are demonstrated. These results demonstrate that phosphors with visible absorption and tunable persistent luminescence lifetimes on the order of hundreds of milliseconds to seconds are attractive for anti-counterfeiting applications as they allow authentication to be performed using only a smartphone. Further development should allow richer color shifts and enhancement of security by embedding further covert anti-counterfeiting features.

A ratiometric optical thermometer based on triply‐doped La2O3:Yb3+/Er3+/Nd3+ microcrystals is reported with a relative sensitivity above 1% K−1 in the entire range from 300–700 K, and is between 1.8–0.7% K−1 over the range 290–833 K. The 825 nm upconversion (UC) emission from the Nd3+ 4F5/2 level relies on thermally‐assisted energy transfer from Yb3+; thus, unusually, the near‐infrared emission increases with increasing temperature in the relevant range. More typically, the two‐photon 660 nm UC from Er3+ 4F9/2 level decreases in intensity with increasing temperature due to increasing non‐radiative rates. The variation of fluorescent intensity ratio between these emissions is amplified by their opposite responses to temperature change leading to excellent sensitivity. Concurrently, the different pathways for the temperature response in the two emitting ions enable the high sensitivity to be maintained over an atypically broad temperature range. The wide separation in wavelength means that a standard silicon‐based monochrome camera with broad (inexpensive) band pass filters is sufficient to use this phosphor for thermography. The concept of combining thermally‐activated UC with classical Stokes‐shifted emission is demonstrated to provide combined features of excellent and broad‐range sensitivity plus excellent repeatability. Materials based on this concept are very promising for optical thermometry.