光电流
光电探测器
材料科学
量子点
光致发光
光电子学
瞬态(计算机编程)
胶体
超快激光光谱学
配体(生物化学)
量子效率
存水弯(水管)
吸收(声学)
光谱学
化学
物理
物理化学
生物化学
受体
量子力学
计算机科学
复合材料
操作系统
气象学
作者
Darshan H. Parmar,Benjamin Rehl,Ozan Atan,Sjoerd Hoogland,Edward H. Sargent
标识
DOI:10.1021/acsami.3c14611
摘要
Colloidal quantum dot (CQD) photodetectors (PDs) can detect wavelengths longer than the 1100 nm limit of silicon because of their highly tunable bandgaps. CQD PDs are acutely affected by the ligands that separate adjacent dots in a CQD-solid. Optimizing the exchange solution ligand concentration in the processing steps is crucial to achieving high photodetector performance. However, the complex mix of chemistry and optoelectronics involved in CQD PDs means that the effects of the exchange solution ligand concentration on device physics are poorly understood. Here we report direct correspondence between simulated and experimental transient photocurrent responses in CQD PDs. For both deficient and excess conditions, our model demonstrated the experimental changes to the transient photocurrent aligned with changes in trap state density. Combining transient photoluminescence, absorption, and photocurrent with this simulation model, we revealed that different mechanisms are responsible for the increased trap density induced by excess and deficient active layer ligand concentrations.
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