During
the last two decades, spectacular development of light-emitting
diodes (LEDs) has been achieved owing to their widespread application
possibilities. However, traditional LEDs suffer from unavoidable energy
loss because of the down conversion of photons, toxicity due to the
involvement of rare-earth materials in their production, higher manufacturing
cost, and reduced thermal stability that prevent them from all-inclusive
applications. To address the existing challenges associated with current
commercially available white LEDs, herein, we report a broad-band
emission originating from an intrinsic lanthanide-free single-molecule-based
LED. Self-assembly of a butterfly-shaped strontium-based compound
{[Sr(H2btc)2(MeOH)(H2O)2]·2H2O} (1) was achieved through the
reaction of Sr(NO3)2 with 1,2,3-benzenetricarboxylic
acid hydrate (1,2,3-H3btc) under hydrothermal conditions.
A white LED based on this single molecule exhibited a remarkable broad-band
luminescence spectrum with Commission Internationale de l’Eclairage
(CIE) coordinates at (0.33, 0.32) under 30 mA current injection. Such
a broad luminescence spectrum can be attributed to the simultaneous
existence of several emission lines originating from the intramolecular
interactions within the structure. To further examine the nature of
the observed transitions, density functional theory (DFT) calculations
were carried out to explore the geometric and electronic properties
of the complex. Our study thus paves the way toward a key step for
developing a basic understanding and the development of high performance
broad-band light-emitting devices with environment-friendly characteristics
based on organic–inorganic supramolecular materials.