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Enhancement of photoluminescence and the stability of CsPbX3 (X = Cl, Br, and I) perovskite nanocrystals with phthalimide passivation

机译:光致发光增强和稳定CsPbX3 (X = Cl, Br,我)钙钛矿纳米晶体与phthalimide钝化

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Cesium lead halide perovskite nanocrystals (CsPbX3 NCs) have been the flourishing area of research in the field of photovoltaic and optoelectronic applications because of their excellent optical and electronic properties. However, they suffer from low stability and deterioration of photoluminescence (PL) properties post-synthesis. In this work, we demonstrate that incorporating an additional ligand can further enhance the optical properties and stability of NCs. Here, we introduced phthalimide as a new surface passivation ligand into the oleic acid/oleylamine system in situ to get near-unity photoluminescence quantum yield (PLQY) of CsPbBr3 and CsPbI3 perovskite NCs. Phthalimide passivation dramatically improves the stability of CsPbCl3, CsPbBr3, and CsPbI3 NCs under ambient light and UV light. The PL intensity was recorded for one year, which showed a dramatic improvement for CsPbBr3 NCs. Nearly 11% of PL can be retained even after one year with phthalimide passivation. CsPbCl3 NCs exhibit 3 times higher PL with phthalimide and retain 12% PL intensity even after two months, while PL of as-synthesized NCs completely diminishes. Under continuous UV light illumination, the PL intensity of phthalimide passivated NCs is well preserved, while the as-synthesized NCs exhibit negligible PL emission in 2 days. About 40% and 25% of initial PL is preserved for CsPbBr3 and CsPbCl3 NCs in the presence of phthalimide. CsPbI3 NCs with phthalimide exhibit PL even after 2 days, while PL for as-synthesized NCs rapidly declined in the first 10 h. The presence of phthalimide in CsPbI3 NCs could maintain stability even after a week, while the as-synthesized NCs underwent a transition to the non-luminescent phase within 4 days. Furthermore, blue, green, yellow, and red-emitting diodes using CsPbCl1.5Br1.5, CsPbBr3, CsPbBr1.5I1.5, CsPbI3 NCs, respectively, are fabricated by drop-casting NCs onto blue LED lights, which show great potential in the field of display and lighting technologies.
机译:铯卤化铅钙钛矿纳米晶体(CsPbX3nc)蓬勃发展的研究领域在光伏领域的光电因其优异的光学应用和电子性质。从低稳定性和恶化光致发光(PL) post-synthesis属性。在这项工作中,我们证明合并一个额外的配体可以进一步提高光学特性和nc的稳定。介绍了phthalimide作为一种新的表面钝化配体到油酸/油酰胺系统原位near-unity光致发光量子产率(PLQY CsPbBr3)和CsPbI3钙钛矿nc。钝化大大提高了稳定性CsPbCl3, CsPbBr3, CsPbI3 nc环境下光和紫外线。一年,显示一个戏剧性的改善对于CsPbBr3 nc。即使一年phthalimide钝化。CsPbCl3 nc展览PL高出3倍phthalimide甚至保留12% PL强度两个月后,而PL as-synthesized nc完全减少。照明,phthalimide的PL强度nc钝化是保存完好,而as-synthesized nc展览PL发射可以忽略不计在2天。保存CsPbBr3和CsPbCl3 ncphthalimide的存在。phthalimide展览PL即使在2天之后,PL的as-synthesized nc迅速下降前10 h。CsPbI3 phthalimide的存在nc可以保持稳定甚至一个星期后,虽然as-synthesized nc接受了在4 non-luminescent过渡阶段天。使用CsPbCl1.5Br1.5 red-emitting二极管,CsPbBr3、CsPbBr1.5I1.5 CsPbI3 nc分别由drop-casting捏造nc在蓝色的领导灯,显示了很大的潜力显示和照明技术。

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