Ionic liquid engineering enables 1D/3D perovskite photovoltaics with > 25 % efficiency: A real-time study exploring formation mechanism of 1D perovskites

被引:1
|
作者
Wang, Fei [1 ,2 ]
Sun, Yonggui [2 ]
Wang, Taomiao [2 ]
Sun, Xiaokang [2 ]
Yang, Guo [2 ]
Li, Yongjun [2 ]
Li, Qiannan [2 ]
Liang, Xiao [1 ,2 ]
Zhou, Xianfang [1 ,2 ]
Lv, Jie [2 ]
Zhu, Quanyao [1 ]
Yang, Chunming [3 ]
Lin, Haoran [2 ]
Yuan, Mingjian [4 ]
Li, Gang [5 ]
Hu, Hanlin [2 ]
机构
[1] Wuhan Univ Technol, Sch Mat Sci & Engn, State Key Lab Adv Technol Mat Synth & Proc, Wuhan, Hubei, Peoples R China
[2] Shenzhen Polytech Univ, Hoffmann Inst Adv Mat, 7098 Liuxian Blvd, Shenzhen 518055, Peoples R China
[3] Chinese Acad Sci, Shanghai Adv Res Inst, Shanghai Synchrotron Radiat Fac, Shanghai 201204, Peoples R China
[4] Nankai Univ, Coll Chem, Tianjin, Peoples R China
[5] Hong Kong Polytech Univ, Res Inst Smart Energy RISE, Dept Elect & Informat Engn, Hung Hom,Kowloon, Hong Kong, Peoples R China
关键词
1D/3D perovskite; In-situ GIWAXS; Ionic liquid; Stability; SOLAR-CELLS; PASSIVATION; LAYER;
D O I
10.1016/j.nanoen.2024.110063
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The advancements in low-dimensional/three-dimensional (LD/3D) perovskite devices represent a promising approach to enhancing both the efficiency and stability of of perovskite solar cells (PSCs). However, while significant efforts have been dedicated to understanding the role of already formed low-dimensional perovskites in passivating defects, refining the work function, little attention has been given to the crystallization process of LD perovskites, particularly when induced by ionic liquids (ILs) as green and stable additive. In this work, the formation process of IL Tetrabutylammonium Thiocyanate (TBASCN)-induced 1D perovskite onto the 3D perovskite under varying annealing conditions were explored by in-situ Grazing-Incidence Wide-Angle X-ray Scattering (GIWAXS) technology, providing a comprehensive investigation into the distinct impacts of 1D perovskite formed under diverse annealing processes on device performance. Owing to the robust interaction and favorable binding energy between the IL TBASCN and perovskite components, coupled with the low formation energy of 1D perovskites, 1D perovskites exhibit rapid formation on the surface of 3D perovskites and display markedly distinct crystallization processes under distinguished annealing conditions. Achieving full crystallization of 1D perovskites necessitates optimal temperature of 100 degrees C and adequate duration of 100 s. Once fully crystallized, the highly crystalline 1D perovskites and anions SCN- present in ILs can synergistically passivate defects in 3D perovskites, mitigate ion migration and impeding moisture infiltration. Benefiting from the optimized formation process of 1D perovskites, the champion device achieves a power conversion efficiencie (PCE) of 25.18 % and retains 91.0 % of its initial efficiency after 2000 h under RH=40 %. Our research provides new insights for optimizing the formation process of LD perovskites induced by different materials and their application in high-performance LD/3D PSCs.
引用
收藏
页数:12
相关论文
共 50 条
  • [1] Ionic Liquid-Induced 1D Perovskite: Exploring 1D Perovskite Structure to 1D/3D Heterojunction-Based Photovoltaics
    Wang, Fei
    Zhou, Kang
    Zhou, Chao
    Liang, Xiao
    Wang, Taomiao
    Sun, Yonggui
    Li, Yongjun
    Li, Qiannan
    Zhou, Xianfang
    Yang, Guo
    Duan, Dawei
    Zhu, Jiajie
    Zhu, Quanyao
    Lin, Haoran
    Shi, Yumeng
    Yang, Chunming
    Xing, Guichuan
    Hu, Hanlin
    ADVANCED ENERGY MATERIALS, 2024, 14 (23)
  • [2] Reducing 3D Vibrations to 1D in Real Time
    Park, Gunhyuk
    Kuchenbecker, Katherine J.
    HAPTIC INTERACTION: PERCEPTION, DEVICES AND ALGORITHMS, 2019, 535 : 21 - 24
  • [3] Cation substitution enables the complete conversion of 1D perovskites to 3D perovskites for photovoltaic application
    Wang, Fuchang
    Li, Weiping
    Liu, Huicong
    Zhu, Liqun
    Chen, Haining
    NANOSCALE, 2019, 11 (30) : 14465 - 14471
  • [4] Formation Dynamics of Thermally Stable 1D/3D Perovskite Interfaces for High-Performance Photovoltaics
    Liang, Lusheng
    Nan, Zi-Ang
    Li, Yuheng
    Zhang, Yi
    Fei, Zhaofu
    Shibayama, Naoyuki
    Zhang, Zilong
    Lin, Zexin
    Chen, Weizhong
    Li, Chi
    Chen, Yong
    Xie, Zhaoxiong
    Dyson, Paul
    Nazeeruddin, Mohammad Khaja
    Gao, Peng
    ADVANCED MATERIALS, 2025, 37 (08)
  • [5] 3D Shape Recognition Based on 1D Signal Processing for Real-Time Applications
    K. Baibai
    K. Hachami
    M. Emharraf
    B. Bellach
    Pattern Recognition and Image Analysis, 2020, 30 : 315 - 327
  • [6] 3D Shape Recognition Based on 1D Signal Processing for Real-Time Applications
    Baibai, K.
    Hachami, K.
    Emharraf, M.
    Bellach, B.
    PATTERN RECOGNITION AND IMAGE ANALYSIS, 2020, 30 (03) : 315 - 327
  • [7] Ionic liquid engineering enabled in-plane orientated 1D perovskite nanorods for efficient mixed-dimensional perovskite photovoltaics
    Wang, Fei
    Duan, Dawei
    Zhou, Kang
    Xue, Y. Z. B.
    Liang, Xiao
    Zhou, Xianfang
    Ge, Chuangye
    Zhou, Chao
    Xiang, Jin
    Zhu, Jiajie
    Zhu, Quanyao
    Lin, Haoran
    Shi, Yumeng
    Chen, Yonghua
    Li, Gang
    Hu, Hanlin
    INFOMAT, 2023, 5 (08)
  • [8] Spontaneous Formation of 1D/3D Perovskite Heterojunctions for Efficient Inverted Perovskite Solar Cells
    Ji, Ran
    Zhang, Zongbao
    Deconinck, Marielle
    Hofstetter, Yvonne J.
    Shi, Juanzi
    Paulus, Fabian
    Raval, Parth
    Reddy, G. N. Manjunatha
    Vaynzof, Yana
    ADVANCED ENERGY MATERIALS, 2024, 14 (20)
  • [9] 1D and 3D shaped ionic Liquid/Aluminum hydroxide nanohybrids for electrochemical device
    Park, Ho Seok
    You, Jong Kyun
    Choi, Bong Gill
    Hong, Won Hi
    Yoo, Ki-Pung
    2007 2ND IEEE INTERNATIONAL CONFERENCE ON NANO/MICRO ENGINEERED AND MOLECULAR SYSTEMS, VOLS 1-3, 2007, : 946 - +
  • [10] Exploring Group 14 Structures: 1D to 2D to 3D
    Wen, Xiao-Dong
    Cahill, Thomas J.
    Hoffmann, Roald
    CHEMISTRY-A EUROPEAN JOURNAL, 2010, 16 (22) : 6555 - 6566