Phase evolution of all-inorganic perovskite nanowires during its growth from quantum dots

2021 ◽  
Author(s):  
Gokul M. A. ◽  
Atikur Rahman

Abstract All-inorganic lead-halide perovskites have emerged as an exciting material owing to their excellent optoelectronic properties and high stability over hybrid organometallic perovskites. Nanowires of these materials, in particular, have shown great promise for optoelectronic applications due to their high optical absorption coefficient and low defect state density. However, the synthesis of the most promising alpha-Cesium lead iodide (α-CsPbI3) nanowires is challenging as it is metastable and spontaneously converts to a non-perovskite δ-phase. The hot-injection method is one of the most facile, well-controlled, and commonly used approaches for synthesizing CsPbX3 nanostructures. But the exact mechanism of growing these nanowires in this technique is not clear. Here, we show that the hot-injection method produces photoactive phases of quantum dots (QDs) and nanowires of CsPbBr3, and QDs of CsPbI3, but CsPbI3 nanowires are grown in their non-perovskite δ-phase. Monitoring the nanowire growth during the hot-injection technique and through detailed characterization, we establish that CsPbI3 nanowires are formed in the non-perovskite phase from the beginning rather than transforming after its growth from perovskite to a non-perovskite phase. We have discussed a possible mechanism of how non-perovskite nanowires of CsPbI3 grow at the expense of photoactive perovskite QDs. Our findings will help to synthesize nanostructures of all-inorganic perovskites with desired phases, which is essential for successful technological applications.

2019 ◽  
Author(s):  
Sofia Masi ◽  
Carlos Echeverría-Arrondo ◽  
Salim K.P. Muhammed ◽  
Thi Tuyen Ngo ◽  
Perla F. Méndez ◽  
...  

<b>The extraordinary low non-radiative recombination and band gap versatility of halide perovskites have led to considerable development in optoelectronic devices. However, this versatility is limited by the stability of the perovskite phase, related to the relative size of the different cations and anions. The most emblematic case is that of formamidinium lead iodine (FAPI) black phase, which has the lowest band gap among all 3D lead halide perovskites, but quickly transforms into the non-perovskite yellow phase at room temperature. Efforts to optimize perovskite solar cells have largely focused on the stabilization of FAPI based perovskite structures, often introducing alternative anions and cations. However, these approaches commonly result in a blue-shift of the band gap, which limits the maximum photo-conversion efficiency. Here, we report the use of PbS colloidal quantum dots (QDs) as stabilizing agent for the FAPI perovskite black phase. The surface chemistry of PbS plays a pivotal role, by developing strong bonds with the black phase but weak ones with the yellow phase. As a result, stable FAPI black phase can be formed at temperatures as low as 85°C in just 10 minutes, setting a record of concomitantly fast and low temperature formation for FAPI, with important consequences for industrialization. FAPI thin films obtained through this procedure preserve the original low band gap of 1.5 eV, reach a record open circuit potential (V<sub>oc</sub>) of 1.105 V -91% of the maximum theoretical V<sub>oc</sub>- and preserve high efficiency for more than 700 hours. These findings reveal the potential of strategies exploiting the chemi-structural properties of external additives to relax the tolerance factor and optimize the optoelectronic performance of perovskite materials.</b>


2014 ◽  
Vol 2 (1) ◽  
pp. 015901 ◽  
Author(s):  
Shenghua Liao ◽  
Yu Huang ◽  
Ying Zhang ◽  
Xiaohui Shan ◽  
Zhengyu Yan ◽  
...  

Nanoscale ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 3246-3251
Author(s):  
Deng-Gui Zhang ◽  
Liang-Yu Jian ◽  
Zong-Liang Tseng ◽  
Hsin-Ming Cheng ◽  
Ja-Hon Lin

Random lasing from CsPbBr3 quantum dots (QDs) prepared by the hot injection method under ambient conditions has been demonstrated. The random laser produced a speckle reduced image with a contrast of around 0.051.


2016 ◽  
Vol 16 (3) ◽  
pp. 2652-2657 ◽  
Author(s):  
Longfei Tan ◽  
Guanbao Huang ◽  
Tianlong Liu ◽  
Changhui Fu ◽  
Yuan Zhou ◽  
...  

2019 ◽  
Author(s):  
Sofia Masi ◽  
Carlos Echeverría-Arrondo ◽  
Salim K.P. Muhammed ◽  
Thi Tuyen Ngo ◽  
Perla F. Méndez ◽  
...  

<b>The extraordinary low non-radiative recombination and band gap versatility of halide perovskites have led to considerable development in optoelectronic devices. However, this versatility is limited by the stability of the perovskite phase, related to the relative size of the different cations and anions. The most emblematic case is that of formamidinium lead iodine (FAPI) black phase, which has the lowest band gap among all 3D lead halide perovskites, but quickly transforms into the non-perovskite yellow phase at room temperature. Efforts to optimize perovskite solar cells have largely focused on the stabilization of FAPI based perovskite structures, often introducing alternative anions and cations. However, these approaches commonly result in a blue-shift of the band gap, which limits the maximum photo-conversion efficiency. Here, we report the use of PbS colloidal quantum dots (QDs) as stabilizing agent for the FAPI perovskite black phase. The surface chemistry of PbS plays a pivotal role, by developing strong bonds with the black phase but weak ones with the yellow phase. As a result, stable FAPI black phase can be formed at temperatures as low as 85°C in just 10 minutes, setting a record of concomitantly fast and low temperature formation for FAPI, with important consequences for industrialization. FAPI thin films obtained through this procedure preserve the original low band gap of 1.5 eV, reach a record open circuit potential (V<sub>oc</sub>) of 1.105 V -91% of the maximum theoretical V<sub>oc</sub>- and preserve high efficiency for more than 700 hours. These findings reveal the potential of strategies exploiting the chemi-structural properties of external additives to relax the tolerance factor and optimize the optoelectronic performance of perovskite materials.</b>


Nanoscale ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 1295-1303 ◽  
Author(s):  
Fanyuan Meng ◽  
Xinyan Liu ◽  
Xinyi Cai ◽  
Zifeng Gong ◽  
Binbin Li ◽  
...  

Rubidium cations (Rb+) can be used to develop blue perovskite quantum dots with simultaneous high photoluminescence and electroluminescence efficiency.


2014 ◽  
Vol 2 (28) ◽  
pp. 5593-5600 ◽  
Author(s):  
Taekeun Kim ◽  
Yun Ku Jung ◽  
Jin-Kyu Lee

The thermal decomposition of Cd(oleate)2, a metal organocarboxylate complex, in the presence of alkylamine was studied in order to understand the formation mechanism of CdSe nanocrystals (quantum dots, QDs) in the hot-injection method.


2017 ◽  
Vol 28 (18) ◽  
pp. 13633-13637 ◽  
Author(s):  
Yueli Liu ◽  
Qiaohui Zhong ◽  
Keqiang Chen ◽  
Jing Zhou ◽  
Xue Yang ◽  
...  

Author(s):  
Junke Jiang ◽  
Feng Liu ◽  
Qing Shen ◽  
Shuxia Tao

Narrow-bandgap CsSnxPb1-xI3 perovskite quantum dots (QDs) show great promise for optoelectronic applications owing to their reduced use of toxic Pb, improved phase stability, and tunable band gaps in the visible...


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