Structure-Dependent Photoluminescence in Low-Dimensional Ethylammonium, Propylammonium, and Butylammonium Lead Iodide Perovskites

2019 ◽  
Vol 12 (4) ◽  
pp. 5008-5016 ◽  
Author(s):  
Chang-Wei Lin ◽  
Fangzhou Liu ◽  
Ting-Yang Chen ◽  
Kuan-Hua Lee ◽  
Chung-Kai Chang ◽  
...  
Keyword(s):  
2019 ◽  
Author(s):  
Noor Titan Putri Hartono ◽  
Shijing Sun ◽  
María Gélvez-Rueda ◽  
Polly Pierone ◽  
Matthew Erodici ◽  
...  

<p>Methylammonium lead iodide (MAPI) is a prototypical photo absorber in perovskite solar cells (PSCs), reaching efficiencies above 20%. However, its hygroscopic nature has prompted the quest to find water-resistant alternatives. Recent studies have suggested that mixing MAPI with lower dimensional, bulky-<i>A</i>-site-cation perovskites helps mitigate this environmental instability. On the other hand, low dimensional perovskites suffer from poor device performance, which has been suggested to be due to limited out-of-plane charge carrier mobility resulting from structural dimensionality and large binding energy of the charge carriers. To understand the effects of dimensionality on performance, we systematically mixed MA-based 3D perovskites with larger <i>A</i>-site cation, dimethylammonium, iso-propylammonium, and t-butylammonium lead iodide perovskites. During the shift from MAPI to lower dimensional (LD) PSCs, the efficiency is significantly reduced by 2 orders of magnitude, with short-circuit currents decreasing from above 20 mA/cm<sup>2</sup> to less than 1 mA/cm<sup>2</sup>. In order to explain these decrease in performance, we studied the charge carrier mobilities of these materials using optical-pump/ terahertz-probe, time-resolved microwave photoconductivity, and photoluminescence measurements. The results show that as we add more of the low dimensional perovskites, the mobility decreases by a factor of 20 when it reaches pure LD perovskites. In addition, the photoluminescence decay fitting is slightly slower for the mixed perovskites, suggesting some improvement in the recombination dynamics. These findings indicate that changes in structural dimensionality by mixing<i> A</i>-site cations play an important role in measured charge carrier mobility, and in the performance of perovskite solar cells.</p>


2017 ◽  
Vol 2017 (47) ◽  
pp. 5539-5544 ◽  
Author(s):  
Hendrik Herrmann ◽  
Petra Walter ◽  
Elisabeth Kaifer ◽  
Hans-Jörg Himmel

2019 ◽  
Vol 7 (15) ◽  
pp. 8811-8817 ◽  
Author(s):  
Chunqing Ma ◽  
Dong Shen ◽  
Bin Huang ◽  
Xiaocui Li ◽  
Wen-Cheng Chen ◽  
...  

One-dimensional perovskites enable high performance low-dimensional perovskite solar cells.


2017 ◽  
Vol 2017 (47) ◽  
pp. 5536-5536
Author(s):  
Hendrik Herrmann ◽  
Petra Walter ◽  
Elisabeth Kaifer ◽  
Hans-Jörg Himmel

2003 ◽  
Vol 67 (15) ◽  
Author(s):  
T. Umebayashi ◽  
K. Asai ◽  
T. Kondo ◽  
A. Nakao

2016 ◽  
Vol 28 (13) ◽  
pp. 4554-4562 ◽  
Author(s):  
Machteld E. Kamminga ◽  
Hong-Hua Fang ◽  
Marina R. Filip ◽  
Feliciano Giustino ◽  
Jacob Baas ◽  
...  

2017 ◽  
Vol 2017 (47) ◽  
pp. 5537-5537
Author(s):  
Hendrik Herrmann ◽  
Petra Walter ◽  
Elisabeth Kaifer ◽  
Hans-Jörg Himmel

2019 ◽  
Author(s):  
Noor Titan Putri Hartono ◽  
Shijing Sun ◽  
María Gélvez-Rueda ◽  
Polly Pierone ◽  
Matthew Erodici ◽  
...  

<p>Methylammonium lead iodide (MAPI) is a prototypical photo absorber in perovskite solar cells (PSCs), reaching efficiencies above 20%. However, its hygroscopic nature has prompted the quest to find water-resistant alternatives. Recent studies have suggested that mixing MAPI with lower dimensional, bulky-<i>A</i>-site-cation perovskites helps mitigate this environmental instability. On the other hand, low dimensional perovskites suffer from poor device performance, which has been suggested to be due to limited out-of-plane charge carrier mobility resulting from structural dimensionality and large binding energy of the charge carriers. To understand the effects of dimensionality on performance, we systematically mixed MA-based 3D perovskites with larger <i>A</i>-site cation, dimethylammonium, iso-propylammonium, and t-butylammonium lead iodide perovskites. During the shift from MAPI to lower dimensional (LD) PSCs, the efficiency is significantly reduced by 2 orders of magnitude, with short-circuit currents decreasing from above 20 mA/cm<sup>2</sup> to less than 1 mA/cm<sup>2</sup>. In order to explain these decrease in performance, we studied the charge carrier mobilities of these materials using optical-pump/ terahertz-probe, time-resolved microwave photoconductivity, and photoluminescence measurements. The results show that as we add more of the low dimensional perovskites, the mobility decreases by a factor of 20 when it reaches pure LD perovskites. In addition, the photoluminescence decay fitting is slightly slower for the mixed perovskites, suggesting some improvement in the recombination dynamics. These findings indicate that changes in structural dimensionality by mixing<i> A</i>-site cations play an important role in measured charge carrier mobility, and in the performance of perovskite solar cells.</p>


Solar Energy ◽  
2018 ◽  
Vol 173 ◽  
pp. 1315-1322 ◽  
Author(s):  
Narayan N. Som ◽  
P.M.W.P. Sampath ◽  
Shweta D. Dabhi ◽  
Venu Mankad ◽  
Satyam Shinde ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Noor Titan Putri Hartono ◽  
Janak Thapa ◽  
Armi Tiihonen ◽  
Felipe Oviedo ◽  
Clio Batali ◽  
...  

Abstract Environmental stability of perovskite solar cells (PSCs) has been improved by trial-and-error exploration of thin low-dimensional (LD) perovskite deposited on top of the perovskite absorber, called the capping layer. In this study, a machine-learning framework is presented to optimize this layer. We featurize 21 organic halide salts, apply them as capping layers onto methylammonium lead iodide (MAPbI3) films, age them under accelerated conditions, and determine features governing stability using supervised machine learning and Shapley values. We find that organic molecules’ low number of hydrogen-bonding donors and small topological polar surface area correlate with increased MAPbI3 film stability. The top performing organic halide, phenyltriethylammonium iodide (PTEAI), successfully extends the MAPbI3 stability lifetime by 4 ± 2 times over bare MAPbI3 and 1.3 ± 0.3 times over state-of-the-art octylammonium bromide (OABr). Through characterization, we find that this capping layer stabilizes the photoactive layer by changing the surface chemistry and suppressing methylammonium loss.


Sign in / Sign up

Export Citation Format

Share Document