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增强空穴传输分子的自组装以制备稳定的倒置钙钛矿太阳能电池。

Reinforcing self-assembly of hole transport molecules for stable inverted perovskite solar cells.

作者信息

Tang Hongcai, Shen Zhichao, Shen Yangzi, Yan Ge, Wang Yanbo, Han Qifeng, Han Liyuan

机构信息

State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai 200240, China.

出版信息

Science. 2024 Mar 15;383(6688):1236-1240. doi: 10.1126/science.adj9602. Epub 2024 Mar 14.

Abstract

Power conversion efficiencies (PCEs) of inverted perovskite solar cells (PSCs) have been improved by the use of a self-assembled monolayer (SAM) hole transport layer. Long-term stability of PSCs requires keeping the SAM compact under the perovskite layer during operation. We found that strong polar solvents in the perovskite precursor desorb the SAM if it is anchored on substrates by hydrogen-bonded, rather than covalently bonded, hydroxyl groups. We used atomic-layer deposition to create an indium tin oxide substrate with a fully covalent hydroxyl-covered surface for SAM anchoring, as well as a SAM with a trimethoxysilane group that exhibited strong tridentate anchoring to the substrate. The resulting PSCs achieved PCEs of 24.8 (certified 24.6) and 23.2% with aperture areas of 0.08 and 1.01 square centimeters, respectively. The devices retained 98.9 and 98.2% of the initial PCE after 1000 hours damp-heat test and operation in maximum power point tracking at 85°C for 1200 hours under standard illumination, respectively.

摘要

通过使用自组装单分子层(SAM)空穴传输层,倒置钙钛矿太阳能电池(PSC)的功率转换效率(PCE)得到了提高。PSC的长期稳定性要求在运行过程中使SAM在钙钛矿层下方保持致密。我们发现,如果SAM通过氢键而非共价键连接的羟基锚定在基底上,钙钛矿前驱体中的强极性溶剂会使SAM解吸。我们使用原子层沉积法制备了一种铟锡氧化物基底,其表面完全被共价键连接的羟基覆盖以用于SAM锚定,还制备了一种带有三甲氧基硅烷基团的SAM,该基团对基底表现出强三齿锚定作用。由此制备的PSC在孔径面积分别为0.08平方厘米和1.01平方厘米时,功率转换效率分别达到24.8%(认证值为24.6%)和23.2%。在标准光照下,经过1000小时湿热测试以及在85°C最大功率点跟踪运行1200小时后,这些器件分别保留了初始PCE的98.9%和98.2%。

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