光探测
钝化
红外线的
配体(生物化学)
量子点
材料科学
胶体
群(周期表)
化学
光电子学
纳米技术
光化学
光电探测器
物理
物理化学
光学
受体
生物化学
有机化学
图层(电子)
作者
Byung Ku Jung,Hyeri Yoo,Bogyeom Seo,Hyung Jin Choi,Young Kyun Choi,Tae Hyuk Kim,Nuri Oh,Soo Young Kim,Sangtae Kim,Yunki Lee,Jae Won Shim,Hye Yeon Park,Gyu Weon Hwang,Tse Nga Ng,Soong Ju Oh
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-01-22
卷期号:9 (2): 504-512
被引量:42
标识
DOI:10.1021/acsenergylett.3c02515
摘要
Group III–V colloidal quantum dots (CQDs) are promising infrared-absorbing materials that overcome the limitations of their regulated heavy-metal-containing counterparts, including Pb-, Cd-, and Hg-based materials. However, their surfaces and ligand chemistry remain unexplored, impeding sufficient ligand exchange. Therefore, approaches for selecting suitable exchange/passivation-enabling ligands for group III–V CQDs must be devised. Based on the hard–soft acid–base theory, diverse metal halide ligands and their interactions with InAs CQD surfaces were scrutinized in this study. Experimental investigations and density functional theory calculations indicated that hard-type Sn-based metal halide ligands exhibited a high affinity for the hard-type As-rich surface of InAs CQDs. Attaching different halides (X) affected the photoresponse performance of InAs-CQD-based devices. Here, high-affinity SnBr2 ligands were selected to fabricate the InAs-CQD-based photodiode, which exhibited the highest external quantum efficiency of 43.1% and responsivity of 0.36 A W–1 at an exciton peak of 1020 nm among previously reported InAs-CQD-based photodiodes.
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