材料科学
光致发光
激发态
激子
结晶度
电子
化学物理
光电子学
凝聚态物理
原子物理学
物理
量子力学
复合材料
作者
Yue Wang,Guodi Zhang,Min Zhao,Hongbo Qi,Tianqi Gao,Limin An,Jianhui Sun
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2024-04-11
卷期号:35 (30): 305702-305702
被引量:1
标识
DOI:10.1088/1361-6528/ad3d63
摘要
Highly-crystallized carbon nitride (HCCN) nanosheets exhibit significant potential for advancements in the field of photoelectric conversion. However, to fully exploit their potential, a thorough understanding of the fundamental excitonic photophysical processes is crucial. Here, the temperature-dependent excitonic photoluminescence (PL) of HCCN nanosheets and amorphous polymeric carbon nitride (PCN) is investigated using steady-state and time-resolved PL spectroscopy. The exciton binding energy of HCCN is determined to be 109.26 meV, lower than that of PCN (207.39 meV), which is attributed to the ordered stacking structure of HCCN with a weaker Coulomb interaction between electrons and holes. As the temperature increases, a noticeable reduction in PL lifetime is observed on both the HCCN and PCN, which is ascribed to the thermal activation of carrier trapping by the enhanced electron-phonon coupling effect. The thermal activation energy of HCCN is determined to be 102.9 meV, close to the value of PCN, due to their same band structures. Through wavelength-dependent PL dynamics analysis, we have identified the PL emission of HCCN as deriving from the transitions:
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