Short‐Wave Infrared Colloidal QD Photodetector with Nanosecond Response Times Enabled by Ultrathin Absorber Layers

Author:

Deng Yu‐Hao12ORCID,Pang Chao23,Kheradmand Ezat12,Leemans Jari12,Bai Jing12,Minjauw Matthias4,Liu Jiayi25,Molkens Korneel123,Beeckman Jeroen25,Detavernier Christophe4,Geiregat Pieter12,Van Thourhout Dries23,Hens Zeger12ORCID

Affiliation:

1. Physics and Chemistry of Nanostructures Group Ghent University Ghent 9000 Belgium

2. Center for Nano and Biophotonics Ghent University Ghent 9052 Belgium

3. Photonics Research Group Ghent University Ghent 9052 Belgium

4. Department of Solid State Sciences Ghent University Ghent 9000 Belgium

5. Department of Electronics and Information Systems Ghent University Ghent 9052 Belgium

Abstract

AbstractUltrafast short‐wavelength infrared (SWIR) photodetection is of great interest for emerging automated vision and spatial mapping technologies. Colloidal quantum dots (QDs) stand out for SWIR photodetection compared to epitaxial (In,Ga)As or (Hg,Cd)Te semiconductors by their combining a size‐tunable bandgap and a suitability for cost‐effective, solution‐based processing. However, achieving ultrafast, nanosecond‐level response time has remained an outstanding challenge for QD‐based SWIR photodiodes (QDPDs). Here, record 4 ns response time in PbS‐based QDPDs that operate at SWIR wavelengths is reported, a result reaching the requirement of SWIR light detection and ranging based on colloidal QDs. These ultrafast QDPDs combine a thin active layer to reduce the carrier transport time and a small area to inhibit slow capacitive discharging. By implementing a concentration gradient ligand exchange method, high‐quality p–n junctions are fabricated in these ultrathin QDPDs. Moreover, these ultrathin QDPDs attain an external quantum efficiency of 42% at 1330 nm, due to a 2.5‐fold enhanced light absorption through the formation of a Fabry–Perot cavity within the QDPD and the highly efficient extraction (98%) of photogenerated charge carriers. Based on these results, it is estimated that a further increase of the charge‐carrier mobility can lead to PbS QDPDs with sub‐nanosecond response time.

Funder

Universiteit Gent

European Research Council

Publisher

Wiley

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