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Zou, S.;  Zhao, X.;  Ouyang, W.;  Xu, S. Microfluidic Synthesis of Halide Perovskite. Encyclopedia. Available online: https://encyclopedia.pub/entry/28960 (accessed on 05 September 2024).
Zou S,  Zhao X,  Ouyang W,  Xu S. Microfluidic Synthesis of Halide Perovskite. Encyclopedia. Available at: https://encyclopedia.pub/entry/28960. Accessed September 05, 2024.
Zou, Shuangyang, Xiaoan Zhao, Wenze Ouyang, Shenghua Xu. "Microfluidic Synthesis of Halide Perovskite" Encyclopedia, https://encyclopedia.pub/entry/28960 (accessed September 05, 2024).
Zou, S.,  Zhao, X.,  Ouyang, W., & Xu, S. (2022, October 12). Microfluidic Synthesis of Halide Perovskite. In Encyclopedia. https://encyclopedia.pub/entry/28960
Zou, Shuangyang, et al. "Microfluidic Synthesis of Halide Perovskite." Encyclopedia. Web. 12 October, 2022.
Microfluidic Synthesis of Halide Perovskite
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This entry is adapted from the peer-reviewed paper 10.3390/mi13101647

Halide perovskites are increasingly exploited as semiconducting materials in diverse optoelectronic applications, including light emitters, photodetectors, and solar cells. The halide perovskite can be easily processed in solution, making microfluidic synthesis possible. 

microfluidics halide perovskite doping nanomaterials

1. Introduction

The microfluidic chip that confines fluids in micron channels can scale the chemical reactions from extensive batch synthesis down to the microscale, exploiting the physical and chemical properties of liquids and gases at a microscale, significantly reducing the synthesis and analysis of volume reagents [1][2][3][4][5]. In nanocrystal (NC) synthetic processes, the batch synthesis strategies of NCs are almost always challenging due to rapid perovskite crystallization, the extensive precursor preparation, the difficulties associated with product purification, and the need for particle post-synthesis. It is envisioned that a microreactor platform consisting of flow-focusing microfluidics might be suitable to synthesize high-crystallinity and narrow-size-distribution NCs due to the ultrafast mixing and phase separation during the crystal nucleation and growth. The microfluidic chemical reactions can be precisely detected and explored by in situ spectroscopy [6][7][8][9][10] and more sufficient and continuous during the reaction on the micron scale. Therefore, there are at least two advantages to microfluidic synthesis. On the macroscopic level, a microreactor can be considered a powerful and effective platform for the mass synthesis of semiconductor nanomaterials. On the microscopic level, the microfluidic technique facilitates the simultaneous collection of both absorption and photoluminescence (PL) spectra of various luminescent materials synthesized in the liquid states, particularly that of halide perovskite nanocrystals.
Quantum dot (QD) semiconductors are promising materials for various applications ranging from light-emitting diode (LED) displays to solar cells, biological sensing, and imaging [6][7][8]. Specifically as optoelectronic materials, perovskite nanocrystals have attracted much more attention due to their high PL quantum yields, high absorption/emission efficiency, long carrier lifetime, and tunable emission color over the entire visible region [9][10][11]. Lead halide perovskite structure can be characterized by the general formula ABX3 (X = Cl, Br, or I), where A and B represent two different cations. A-site cations can be inorganic or organic ions, such as cesium (Cs), formamidinium (FA), and methylammonium (MA), while B-site cation (Pb2+) could potentially be exchanged by dopant ions (Mn2+, Fe2+, Ce3+, Eu2+) [12][13][14][15][16][17][18]. Therefore, the hybrid organic−inorganic lead halide perovskite, such as CH3NH3PbX3; and all inorganic lead halide perovskite, such as CsPbX3, in the form of nanocrystals, thin films, microcrystals, and bulk single-crystals, show promising properties in LEDs [9][19], lasers [20], solar cells [21][22][23], gas sensors [24], etc.

2. Microfluidic Synthesis of Halide Perovskite

Generally, microfluidic devices have microchannels ranging from submicron to a few millimeters. For various microfluidic syntheses of perovskite nanostructures and composite, which can move or analyze the tiny amount of liquid (droplet) in a single- or multi-phase flow.
The microfluidic reaction has been recognized to be more controllable and continuous during the nanostructure’s synthesis on the microscale. As shown in schematic of the PL dynamics of microfluidic droplet, the QDs were synthesized from multiphase (liquid, gas) in microfluidic channels. Compared to conventional flask synthesis under gas protection at high temperatures, the continuous-flow microfluidic approach benefits the alignment of the quantum-confined perovskite nanocrystals and can promote crystal growth orientation to form long nanowires (NWs) at room temperature. Reagent precursor solution is injected into the microchannel. After combination in the channel, different types of nanomaterials can be achieved (Table 1) [25][26][27][29][31][32][33].
Table 1. Microfluidic synthesis of nanostructured halide perovskite.
Materials Synthesis Temp. (°C) Size PL Peak Location (nm) Year [Ref.]
CsPbBr3 QDs RT <10 nm ~500 2017, Epps et al. [33]
CsPbBr3 QDs RT 10–20 nm ~520 2019, Wei et al. [34]
CsPbBr3 NWs 50 3–9 μm 535 2021, Koryakina et al. [29]
CsPbBr3 NWs 50 ~4 nm (width) ~475 2019, Zhang et al. [31]
MAPbI3 85 60 μm (width) - 2020, Khorramshahi et al. [35]
QD encapsulation 37 500–700 nm 430–625 2021, Bian et al. [32]
MAPbBr3 composite - 500 μm ~530 2021, Kim et al. [26]
FAPb(I/Br)3 QDs 120 ~10 nm 530–690 2017, Maceiczyk et al. [36]
Cs4PbBr6 MCs 60–150 >1 μm 520 2018, Bao et al. [37]
CsPbX3 QDs 130–220 8–12.5 nm 470–690 2016, Lignos et al. [38][39][40]
CsPbX3 QDs RT <20 nm 422–660 2019, Abdel-Latif et al. [30]
CsPbX3 NCs RT ~15 nm ~520 2020, Lin et al. [41]
CsPbX3 NCs 100–180 <20 nm 406–677 2022, Geng et al. [42]
In the materials column of the table, QDs: quantum dots, NCs: nanocrystals, NWs: nanowires, MCs: microcrystals, and X = Br, I, Cl, respectively.
The microfluidic channel with controllable morphology and configuration could be efficiently designed and achieved, therefore, nanomaterials could be more precisely synthesized in the microfluidic channel. For example, Kim et al. reported the in situ reaction of metal halide perovskite nanoparticles by the ligand-assisted reprecipitation process (LARP) and encapsulation by ultraviolet light (UV) cross-linking polymerization, in which the stable, water-resistant light-emitting perovskite–polymer composite microparticles can be synthesized in a continuous one-step microfluidic reactor [26]. Tuning the reactant concentration and the flow rate in the microreactor, ranging from several nanometers to over one hundred nanometers, hollow spherical silica-based functional materials and the Cs4PbBr6 perovskite microcrystals (MCs) were synthesized by mixing two reactant flows, respectively [25][37]. With the microfluidic template, well-aligned and uniform heterojunctions of MAPbI3 and organic semiconductors (OSC) in the silicon nanowire patterns can be grown. Different morphologies (1D, 2D) of halide perovskite have already been successfully synthesized via solution methods [17][43][44], which are difficult to batch produce and industrially apply in comparison to microfluidic synthesis. In continuous anion exchange reactions of CsPbBr3 QDs, the halide exchange reactions are realized in a modular microfluidic platform called Quantum Dot Exchanger, which offers a unique time- and material-efficient approach for studies of solution phase-processed colloidal nanocrystals [30][45][46]. Perovskite precursor solutions could be simultaneously pumped into the microfluidic device. By changing the ratio of different perovskite precursor solutions, a series of perovskite QDs can be precipitated and encapsulated in ethyleneglycol dimethacrylate (EGDMA) resin [32]. The microfluidic synthesis makes chemical composition tuning and doping in perovskite more available.

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Subjects: Nanoscience & Nanotechnology
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Shuangyang Zou
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Xiaoan Zhao
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Wenze Ouyang
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Shenghua Xu
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Update Date: 12 Oct 2022
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