skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Explore Research Products in the PAR
It may take a few hours for recently added research products to appear in PAR search results.


  • NSF Public Access
  • Search Results
  • Enhancing Uniform Crystallization and Grain Growth of Halide Perovskite Films by Combining Multipass Inkjet Printing and Antisolvent Bathing
Title: Enhancing Uniform Crystallization and Grain Growth of Halide Perovskite Films by Combining Multipass Inkjet Printing and Antisolvent Bathing
Recent manufacturing of perovskite solar cells (PSC) is moving beyond a spin coating technique. Among several new methods of the large‐area PSCs, inkjet printing (IJP) has emerged as a promising alternative to spin coating due to the high degree of control on printed film area and low material waste. In the IJP of PSCs, one important question is how to remove redundant excess solvent and facilitate the crystallization of the perovskite phase. Along with IJP, an antisolvent bathing is employed. This work reports how the IJP parameters and antisolvent bathing compositions affect the microstructure and initial efficiency of inkjet‐printed PSCs. The halide perovskite films are submerged in the antisolvent of different temperatures to observe the formation of an intermediate phase and the evolution of perovskite phase. By observing the phase evolution using X‐Ray diffraction, an optimized antisolvent bath duration is achieved for diethyl ether (DE) condition. An enhanced power conversion efficiency (PCE) and larger grain size with two sequential passes of inkjet‐deposited perovskite are also reported, and the dissolution of homogeneous nucleation sites as a mechanism for larger grains is proposed. Finally, with multipass IJP and cold antisolvent DE bathing, a champion device with 15.02% PCE is achieved.  more » « less
Award ID(s):
2314036 2130804
PAR ID:
10557130
Author(s) / Creator(s):
 ;  ;  ;  ;  
Publisher / Repository:
Wiley Blackwell (John Wiley & Sons)
Date Published:
Journal Name:
Advanced Energy and Sustainability Research
Volume:
6
Issue:
1
ISSN:
2699-9412
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. ; (, Energies)
    Perovskite photovoltaic technology carries immense opportunity for the solar industries because of its remarkable efficiency and prospect for cost-effective production. However, the successful deployment of perovskite solar modules (PSMs) in the solar market necessitates tackling stability-based obstacles, scalability, and environmental considerations. This paper unveils a comprehensive examination of the cutting-edge advancements in the manufacturing of perovskite solar cells (PSCs) and modules, with an emphasis on high-speed, large-area printing. The paper underscores the substantial progress achieved in printed PSCs and PSMs, demonstrating promising electrical performance and long-term device durability. This review paper categorizes printing techniques compatible with large-area high-speed manufacturing into three distinct families: blade coating, slot die coating, and screen printing, as these common printing practices offer precise control, scalability, cost-effectiveness, high resolution, and efficient material usage. Additionally, this paper presents an in-depth investigation and comparison of superior PSCs and PSMs fabricated by printing on power conversion efficiency (PCE), stability, and scalability. 
    more » « less
  2. ; ; ; ; ; ; ; ; ; ; et al (, Small)
    Abstract Dimethylammonium lead iodide (DMAPbIx) has the potential to address the phase stability issue of inorganic perovskite solar cells (PSCs). In this study, the crystallinity, phase structure, defect states, and crystal growth habits of DMAPbIxare controlled by adjusting thexvalue during synthesis, where N,N‐dimethylacetamide (DMAC) is used as the solvent to regulate perovskite film growth. Furthermore, large‐area CsPbI2.85Br0.15perovskite films with preferred oriented growth are achieved using the optimizedxvalue in DMAPbIxthrough the slot‐die coating method. The inorganic PSCs, with a n‐i‐p structure and the active area of 0.04 cm2, achieve a champion power conversion efficiency (PCE) of 19.82%, with an open‐circuit voltage (Voc) of 1.16 V based on perovskite films formed by slot‐die coating. This work provides important insights into the DMAPbIx‐based method for fabricating high‐quality inorganic perovskite films, and paves the way for large‐area inorganic PSCs fabrication for practical applications. 
    more » « less
  3. ; ; ; ; (, Energy Technology)
    Rapid chemistry and processing development has increased the performance of perovskite solar cells (PSCs) in an unprecedented manner, yet postdeposition annealing impedes high‐throughput manufacturing. Herein, SnO2and carbon charge transport films are fabricated entirely through an integrated robotic setup utilizing inkjet printing and intense pulse light (IPL) as a high‐speed postprocess annealing method; hence, process optimization is crucial for successful fabrication of PSCs. This work investigates the role of inkjet deposition parameters as well as IPL annealing on the morphology and uniformity of films with aid of spectroscopy and spectrophotometry. Initially PSCs exceeding 13% efficiency are developed by only fabricating the SnO2film through the robotic setup, but spin coating all other films followed by IPL annealing to demonstrate successful fabrication of SnO2layer. Finally, SnO2and carbon back contact films are entirely fabricated through the integrated robotic setup in a high humid ambient environment (>60%), resulting in PSCs exceeding 5% efficiency. Unlike successful direct annealing of SnO2wet films, IPL annealing of wet carbon severely damaged the phase and morphology necessitating rapid solvent removal before IPL annealing. This work establishes pioneering steps towards utilizing IPL in an entirely automated fabrication line, allowing for scalable fabrication of PSCs through non‐roll‐to‐roll. 
    more » « less
  4. ; ; ; ; ; ; ; ; ; ; et al (, Angewandte Chemie International Edition)
    Abstract Surface passivation of perovskite solar cells (PSCs) using a low‐cost industrial organic pigment quinacridone (QA) is presented. The procedure involves solution processing a soluble derivative of QA,N,N‐bis(tert‐butyloxycarbonyl)‐quinacridone (TBOC‐QA), followed by thermal annealing to convert TBOC‐QA into insoluble QA. With halide perovskite thin films coated by QA, PSCs based on methylammonium lead iodide (MAPbI3) showed significantly improved performance with remarkable stability. A PCE of 21.1 % was achieved, which is much higher than 18.9 % recorded for the unmodified devices. The QA coating with exceptional insolubility and hydrophobicity also led to greatly enhanced contact angle from 35.6° for the pristine MAPbI3thin films to 77.2° for QA coated MAPbI3thin films. The stability of QA passivated MAPbI3perovskite thin films and PSCs were significantly enhanced, retaining about 90 % of the initial efficiencies after more than 1000 hours storage under ambient conditions. 
    more » « less
  5. ; ; ; ; ; ; ; ; ; (, Advanced Materials)
    Abstract The performance of large‐area perovskite solar cells (PSCs) has been assessed for typical compositions, such as methylammonium lead iodide (MAPbI3), using a blade coater, slot‐die coater, solution shearing, ink‐jet printing, and thermal evaporation. However, the fabrication of large‐area all‐inorganic perovskite films is not well developed. This study develops, for the first time, an eco‐friendly solvent engineered all‐inorganic perovskite ink of dimethyl sulfoxide (DMSO) as a main solvent with the addition of acetonitrile (ACN), 2‐methoxyethanol (2‐ME), or a mixture of ACN and 2‐ME to fabricate large‐area CsPbI2.77Br0.23films with slot‐die coater at low temperatures (40–50 °C). The perovskite phase, morphology, defect density, and optoelectrical properties of prepared with different solvent ratios are thoroughly examined and they are correlated with their respective colloidal size distribution and solar cell performance. The optimized slot‐die‐coated CsPbI2.77Br0.23perovskite film, which is prepared from the eco‐friendly binary solvents dimethyl sulfoxide:acetonitrile (0.8:0.2 v/v), demonstrates an impressive power conversion efficiency (PCE) of 19.05%. Moreover, the device maintains ≈91% of its original PCE after 1 month at 20% relative humidity in the dark. It is believed that this study will accelerate the reliable manufacturing of perovskite devices. 
    more » « less
  • Citation Formats
  • MLA
  • APA
  • Chicago
  • BibTeX
  • Save / Share this Record
  • Send to Email