Top‐Down Induced Crystallization Orientation toward Highly Efficient p‐i‐n Perovskite Solar Cells

Author:

Jiang Xiaofen123,Liu Baoze2,Wu Xin2,Zhang Shoufeng2,Zhang Dong2,Wang Xue123,Gao Shuang1,Huang Zongming4,Wang Haolin1,Li Bo2,Xiao Zhengguo4,Chen Tao1,Jen Alex K.‐Y.235,Xiao Shuang6,Yang Shangfeng1,Zhu Zonglong2357ORCID

Affiliation:

1. Key Laboratory of Precision and Intelligent Chemistry Collaborative Innovation Center of Chemistry for Energy Materials (iChEM) Anhui Laboratory of Advanced Photon Science and Technology Department of Materials Science and Engineering University of Science and Technology of China Hefei 230026 China

2. Department of Chemistry City University of Hong Kong Kowloon 999077 Hong Kong

3. Department of Materials Science and Engineering City University of Hong Kong Kowloon 999077 Hong Kong

4. CAS Key Laboratory of Strongly‐coupled Quantum Matter Physics Department of Physics University of Science and Technology of China Hefei 230026 China

5. Hong Kong Institute for Clean Energy City University of Hong Kong Kowloon 999077 Hong Kong

6. Shenzhen Key Laboratory of Ultraintense Laser and Advanced Material Technology Center for Intense Laser Application Technology (iLaT) and College of Engineering Physics Shenzhen Technology University Shenzhen 518118 China

7. City University of Hong Kong Shenzhen Research Institute Shenzhen Guangdong 518057 China

Abstract

AbstractCrystallization orientation plays a crucial role in determining the performance and stability of perovskite solar cells (PVSCs), whereas effective strategies for realizing oriented perovskite crystallization is still lacking. Herein, a facile and efficient top‐down strategy is reported to manipulate the crystallization orientation via treating perovskite wet film with propylamine chloride (PACl) before annealing. The PA+ ions tend to be adsorbed on the (001) facet of the perovskite surface, resulting in the reduced cleavage energy to induce (001) orientation‐dominated growth of perovskite film and then reduce the temperature of phase transition, meanwhile, the penetrating Cl ions further regulate the crystallization process. As‐prepared (001)‐dominant perovskite films exhibit the ameliorative film homogeneity in terms of vertical and horizontal scale, leading to alleviated lattice mismatch and lowered defect density. The resultant PVSC devices deliver a champion power conversion efficiency (PCE) of 25.07% with enhanced stability, and the unencapsulated PVSC device maintains 95% of its initial PCE after 1000 h of operation at the maximum power point under simulated AM 1.5G illumination.

Funder

Innovation and Technology Fund

National Natural Science Foundation of China

Publisher

Wiley

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