钝化
光电探测器
卤化物
材料科学
钙钛矿(结构)
暗电流
光电子学
二硫化钼
比探测率
猝灭(荧光)
光致发光
图层(电子)
纳米技术
光学
无机化学
物理
化学工程
荧光
复合材料
工程类
化学
作者
Haoliang Wang,Xudong Wang,Yan Chen,Shukui Zhang,Wei Jiang,Xin Zhang,Jiajun Qin,Jiao Wang,Xiaoguo Li,Yiyi Pan,Fengcai Liu,Zejiao Shi,Haijuan Zhang,Luqi Tu,Hailu Wang,Huabao Long,Dapeng Li,Tie Lin,Jianlu Wang,Yiqiang Zhan,Hong Shen,Xiangjian Meng,Junhao Chu
标识
DOI:10.1002/adom.201901402
摘要
Abstract Toward pursuing high‐performance photodetectors based on 2D transition metal dichalcogenides (TMDs) such as molybdenum disulfide (MoS 2 ), it is desirable to reduce the high dark current and sluggish response time. Here, in multilayer MoS 2 ‐based photodetectors, a 2D halide perovskite, (C 6 H 5 C 2 H 4 NH 3 ) 2 PbI 4 ((PEA) 2 PbI 4 ), is introduced as a bifunctional material: both as electron reservoir to reduce free carriers and passivation agent to passivate defects. Surprisingly, dark current is suppressed by six orders of magnitude after coating a (PEA) 2 PbI 4 thin layer onto pristine MoS 2 photodetector, with the dark current decreased to 10 −11 A. This huge reduction of dark current suggests an efficient interlayer charge transfer from MoS 2 to (PEA) 2 PbI 4 , which is further verified by photoluminescence quenching phenomenon. It indicates that (PEA) 2 PbI 4 serves as electron reservoir to reduce carrier density of MoS 2 , resulting in ultrahigh detectivity (1.06 × 10 13 Jones). Moreover, the response speed is also accelerated by more than 100‐fold due to passivation by 2D perovskite. In addition, it is found that this type of photodetectors can further work at self‐power mode (with the bias of 0 V). Therefore, the strategy of applying 2D perovskite on the surface of TMDs provides a novel way to fabricate high‐performance photodetectors.
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