光电探测器
杰纳斯
光电子学
材料科学
量子效率
物理
纳米技术
作者
Hengwei Qiu,Yongqiang Ji,Weiyan Hu,Feiyang Liu,Donglin Jia,Lin Zhang,Xiaojun Lv,Meicheng Li
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-03-04
标识
DOI:10.1021/acs.nanolett.4c06595
摘要
Heteronanocrystals (HNCs) composed of colloidal lead halide perovskites and chalcogenides always offer unique photoelectric properties. Nevertheless, synthesizing perovskite-chalcogenide HNCs has been a tough challenge due to their completely different growth dynamics. Here, we present an effective strategy to synthesize Janus CsPbBr3-AgBiS2 HNCs by in situ growth of CsPbBr3 NCs on prepared AgBiS2 quantum dot (QDs). The as-synthesized HNCs show a large range of absorption characteristics from visible to near-infrared (NIR) wavebands. Femtosecond transient absorption (TA) spectroscopy reveals the transfer of both electron and hole from CsPbBr3 to AgBiS2. The enhanced absorption range and exciton dissociation in 150 °C HNCs leads to photoconductors with drastically improved responsivity (R of 183.8 A W-1) and specific detectivity (D* of 5.0 × 1014 Jones). This work not only provides a reliable method for combining ionic CsPbBr3 and covalent AgBiS2 but also has great potential for future practical applications, such as an NC (QD) solar cell.
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