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Highly luminescent and stable bright-blue CH3NH3Pb(Cl/Br)3 perovskite quantum dots with in-situ formed silica shell
被引:1
|作者:
Yang, Mu
[1
,2
]
Dai, Qilin
[3
]
Tang, Aiwei
[1
]
Teng, Feng
[1
]
Peng, Hong-shang
[2
]
机构:
[1] Beijing Jiaotong Univ, Inst Optoelect Technol, Key Lab Luminescence & Opt Informat, Minist Educ, Beijing 100044, Peoples R China
[2] Minzu Univ China, Sch Sci, Beijing 100081, Peoples R China
[3] Jackson State Univ, Dept Chem Phys & Atmospher Sci, Jackson, MS 39217 USA
关键词:
CH3NH3Pb(Cl;
Br)3;
Postsynthetic;
Silica shell;
Defect passivation;
Photostability;
LIGHT-EMITTING-DIODES;
ANION-EXCHANGE;
EFFICIENT;
NANOCRYSTALS;
CSPBX3;
BR;
CL;
EMISSION;
D O I:
10.1016/j.materresbull.2022.112049
中图分类号:
T [工业技术];
学科分类号:
08 ;
摘要:
Current chloride-bromine mixed perovskite quantum dots (PQDs) suffered from low luminescence efficiency and instability due to migration-nature of ionic species and high defect density. To tackle these challenges, herein a novel type of CH3NH3Pb(Cl/Br)3 PQDs (Cl/Br-PQDs) were synthesized via a two-step method. Briefly, pristine silane-capped Br-PQDs were prepared, followed by anion exchange using oleylammonium chloride (OAm-Cl) and in-situ formation of silica shell. The optimal feeding ratio of Cl/Br was determined to be 1:1, which yielded colloidal Cl/Br-PQDs possessing a strong 464-nm emission, a high photoluminescence quantum yield of 94.6% and ultrahigh stability. The high quantum yield was attributed to efficient defects passivation by doped Cl- ions and silica-shell-locked OAm+ ligands, whilst the high stability was to silica-shell-restricted migration of halogen ions. Such a combinational strategy of anion exchange and in-situ growth of silica shell may provide an effective solution for synthesis of mixed PQDs with high quality.
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页数:6
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