Compound Quantum Dot-Perovskite Optical Absorbers on Graphene Enhancing Short-Wave Infrared Photodetection

被引:94
|
作者
Bessonov, Alexander A. [1 ]
Allen, Mark [1 ]
Liu, Yinglin [1 ]
Malik, Surama [1 ]
Bottomley, Joseph [1 ]
Rushton, Ashley [1 ]
Medina-Salazar, Ivonne [1 ]
Voutilainen, Martti [2 ]
Kallioinen, Sami [2 ]
Colli, Alan [1 ]
Bower, Chris [1 ]
Andrew, Piers [1 ]
Ryhanen, Tapani [2 ]
机构
[1] Emberion Ltd, Sheraton House,Castle Pk, Cambridge CB3 0AX, England
[2] Emberion Oy, Metsanneidonkuja 8, Espoo 02130, Finland
关键词
quantum dots; organometal halide perovskite; infrared absorber; graphene phototransistor; sensitivity-response speed trade-off; CHARGE-TRANSPORT; THIN-FILMS; HYBRID STRUCTURES; LIGHT DETECTION; PBS; PHOTOTRANSISTORS; HALIDE; NANOCRYSTALS; DEGRADATION; DIFFUSION;
D O I
10.1021/acsnano.7b00760
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Colloidal quantum dots (QDs) combined with a graphene charge transducer promise to provide a photoconducting platform with high quantum efficiency and large intrinsic gain, yet compatible with cost-efficient polymer substrates. The response time in these devices is limited, however, and fast switching is only possible by sacrificing the high sensitivity. Furthermore, tuning the QD size toward infrared absorption using conventional organic capping ligands progressively reduces the device performance characteristics. Here we demonstrate methods to couple large QDs (>6 nm in diameter) with organometal halide perovskites, enabling hybrid graphene photo transistor arrays on plastic foils that simultaneously exhibit a specific detectivity of 5 X 10(12) Jones and high video-frame-rate performance. PbI2, and CH3NH3I co-mediated ligand exchange in PbS QDs improves surface passivation and facilitates electronic transport, yielding faster charge recovery, whereas Pbs QDs embedded into a CH3NH3PbI3 matrix produce spatially separated photocarriers leading to large gain.
引用
收藏
页码:5547 / 5557
页数:11
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