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Metal nanoclusters (NCs) are considered ideal nanomaterials for biological applications owing to their strong photoluminescence (PL), excellent photostability, and good biocompatibility. This study presents a simple and versatile strategy to design proteins, via incorporation of a di‐histidine cluster coordination site, for the sustainable synthesis and stabilization of metal NCs with different metal composition. The resulting protein‐stabilized metal NCs (Prot‐NCs) of gold, silver, and copper are highly photoluminescent and photostable, have a long shelf life, and are stable under physiological conditions. The biocompatibility of the clusters was demonstrated in cell cultures in which Prot‐NCs showed efficient cell internalization without affecting cell viability or losing luminescence. Moreover, the approach is translatable to other proteins to obtain Prot‐NCs for various biomedical applications such as cell imaging or labeling. [ABSTRACT FROM AUTHOR]

Abstract: State‐of‐the‐art near‐infrared lasers based on poly[N‐9′‐heptadecanyl‐2,7‐carbazole‐alt‐5,5‐(4′,7′‐di‐2‐thienyl‐2′,1′,3′‐benzothiadiazole)] (PCDTBT) and poly(9,9‐dioctylfluorene‐alt‐benzothiadiazole) (F8BT) blends are reported. Polymer light‐emitting diodes (PLEDs) based on PCDTBT/F8BT blends with 30 wt% PCDTBT content exhibit a maximum radiance of 64.3 W sr−1 m−2 and external quantum efficiency of 2.11% with Commission Internationale de L'Eclairage (CIE) coordinates (x = 0.69, y = 0.30). Using an optimal blend ratio of 15 wt% PCDTBT in F8BT, a maximum gain value of 28.2 cm−1 at 710 nm is achieved, a remarkable value given that PCDTBT is a low emissive polymer extensively employed as donor polymer in organic photovoltaics. The lowest amplified spontaneous emission (ASE) and laser thresholds exhibited by the blends are 590 nJ pulse−1 (21 µJ cm−2) and 63.1 nJ pulse−1 (201 µJ cm−2). Transient absorption spectroscopy confirms efficient Förster resonant energy transfer from F8BT to PCDTBT which, together with the large miscibility of PCDTBT in F8BT, enables PCDTBT emission enhancement and optical gain. Furthermore, a ternary blend system composed of F8BT, PCDTBT, and poly(3‐hexylthiophene) is demonstrated, in which the ASE wavelength can be tuned in a 60 nm range from 650 to 710 nm at a very low threshold level via control of the blend content ratio. [ABSTRACT FROM AUTHOR]