2021
DOI: 10.1016/j.mtphys.2021.100513
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The effect of defects in tin-based perovskites and their photovoltaic devices

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Cited by 24 publications
(30 citation statements)
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“…Similarly, the calculated trap densities of the fabricated electron-only devices are 5.5 × 10 15 and 2.7 × 10 15 cm –3 for CB–PVK and CB+PC–PVK, respectively. Thus, the reduced defect density in CB+PC–PVK can suppress nonradiative recombination in the film, , which could be due to the formation of perovskite seeds for templated perovskite growth.…”
Section: Resultsmentioning
confidence: 99%
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“…Similarly, the calculated trap densities of the fabricated electron-only devices are 5.5 × 10 15 and 2.7 × 10 15 cm –3 for CB–PVK and CB+PC–PVK, respectively. Thus, the reduced defect density in CB+PC–PVK can suppress nonradiative recombination in the film, , which could be due to the formation of perovskite seeds for templated perovskite growth.…”
Section: Resultsmentioning
confidence: 99%
“…Similarly, the calculated trap densities of the fabricated electron-only devices are 5.5 × 10 15 and 2.7 × 10 15 cm −3 for CB−PVK and CB+PC−PVK, respectively. Thus, the reduced defect density in CB+PC−PVK can suppress nonradiative recombination in the film,39,40 which could be due to the formation of perovskite seeds for templated perovskite growth.Moreover, steady-state photoluminescence (PL) and timeresolved photoluminescence (TRPL) studies were conducted to investigate the charge-carrier dynamics of perovskite films treated with different antisolvents (Figure3g, h). Although steady-state PL, CB−PVK, and CB+PC−PVK exhibit the same emission at around 778 nm, the latter has a much higher PL intensity.…”
mentioning
confidence: 99%
“…TTF−BTD derivative was synthesized by the method that mentioned above. [1,3]dithiole-2-thione (3 g, 14 mmol) and triethylamine (25 mL) in dichloromethane (300 mL). After addition, the reaction mixture was heated to reflux for 6 h. The solution was cooled and concentrated in a vacuum followed by trituration in water (100 mL) and the product was extracted with dichloromethane (300 mL).…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…The combined organic phase was washed with water (200 mL), saturated NaHCO 3 (aq) (200 mL), 1 M Na 2 SO 3 (aq) (200 mL), and then dried with MgSO 4 . The solvent was evaporated under reduced pressure and the crude product was recrystallized from ethanol, then solubilized in chloroform (30 mL), and passed through a plug of silica gel to afford 4,8dibromo- [1,3] c][1,2,5]thiadiazole-6-thione (4 g, 10 mmol) in a triethyl phosphite (50 mL, freshly distilled) and the reaction mixture was stirred for 2 h at 100− 105 °C. After cooling to room temperature, the precipitate was collected, washed with methyl alcohol, and dried to give methyl 2-(4,8-dibromo- [1,3] 4).…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
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