A construction strategy for ratiometric fluorescent nanosensors based on water soluble C-dots was developed, which could sense temperature (10-82 °C), pH values (lower than 6.0 or higher than 8.6) and Fe(3+) ions (>0.04 μM) by monitoring the intensity ratios of dual fluorescence bands (Ib/Ig) under 380 nm excitation. Ib/Ig decreased nearly linearly with increasing temperature from 10 to 82 °C. In the pH range from 8.6 to 6.0, the Ib/Ig was nearly constant at 0.75. Ib/Ig gradually decreased from 0.75 to 0.52 in the pH range from 6.0 to 1.9, and increased nearly linearly from 0.52 to 0.75 in the pH range from 1.9 to 1.0. The dual fluorescence behavior was reversible in the pH range from 1.0 to 8.6. As pH increased from 10.6 to 13.0, the green fluorescence band decreased continuously and blue shifted with a nearly linear increase in Ib/Ig from 0.75 to 2.15, while the green fluorescence band cannot be recovered by decreasing the pH value. Ib/Ig was ultrasensitive and selective in presence of Fe(3+) (>0.04 μM) in neutral aqueous environments. The two fluorescence bands of the C-dots were attributed to different surface states that may produce different fluorescent signal responses to external physical or chemical stimuli.

In this work, two Cu(II) complex compounds are designed and synthesized for applications as p-type dopants in solid-state perovskite solar cells (PSCs). Through the characterization of the optical and electrochemical properties, the complex Cu(bpcm) 2 is shown to be eligible for oxidization of the commonly used hole-transport material (HTM) Spiro-OMeTAD. The reason is the electron-withdrawing effect of the chloride groups on the ligands. When the complex was applied as p-type dopant in PSCs containing Spiro-OMeTAD as HTM, an efficiency as high as 18.5% was achieved. This is the first time a Cu(II) pyridine complex has been used as p-type dopant in PSCs.

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