异质结
外延
材料科学
范德瓦尔斯力
锑
卤化物
激子
钙钛矿(结构)
光电子学
纳米技术
化学物理
图层(电子)
凝聚态物理
化学
结晶学
无机化学
物理
有机化学
分子
冶金
作者
Zhicheng Zhou,Juntong Zhu,Lutao Li,Wang Chen,Changwen Zhang,Xinyu Du,Xiangyi Wang,Guoxiang Zhao,Ruonan Wang,Jiating Li,Zheng Lu,Yi Zong,Yinghui Sun,Mark H. Rümmeli,Guifu Zou
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-06-21
卷期号:18 (26): 17282-17292
标识
DOI:10.1021/acsnano.4c05293
摘要
Epitaxial growth stands as a key method for integrating semiconductors into heterostructures, offering a potent avenue to explore the electronic and optoelectronic characteristics of cutting-edge materials, such as transition metal dichalcogenide (TMD) and perovskites. Nevertheless, the layer-by-layer growth atop TMD materials confronts a substantial energy barrier, impeding the adsorption and nucleation of perovskite atoms on the 2D surface. Here, we epitaxially grown an inorganic lead-free perovskite on TMD and formed van der Waals (vdW) heterojunctions. Our work employs a monomolecular membrane-assisted growth strategy that reduces the contact angle and simultaneously diminishing the energy barrier for Cs3Sb2Br9 surface nucleation. By controlling the nucleation temperature, we achieved a reduction in the thickness of the Cs3Sb2Br9 epitaxial layer from 30 to approximately 4 nm. In the realm of inorganic lead-free perovskite and TMD heterojunctions, we observed long-lived interlayer exciton of 9.9 ns, approximately 36 times longer than the intralayer exciton lifetime, which benefited from the excellent interlayer coupling brought by direct epitaxial growth. Our research introduces a monomolecular membrane-assisted growth strategy that expands the diversity of materials attainable through vdW epitaxial growth, potentially contributing to future applications in optoelectronics involving heterojunctions.
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