Surfactant-assisted colloidal size and charge control in perovskite solutions for high-performance and stable solar cells
Solution-based lead halide perovskites have achieved remarkable success in both solar cell performance and market potential. However, limited attention has been given to the colloidal properties of perovskite precursor solutions, which are critical for achieving high performance. This study introduces a method to control colloidal charge and size in perovskite solutions using surfactants, thereby enhancing both solar cell performance and stability. The surfactant dodecyltrimethylammonium bromide (DTAB), featuring a positively charged ammonium head group and a long alkyl chain, induces the formation of smaller, positively charged perovskite colloids. These modified colloids promote slow, homogeneous crystallization, resulting in high-quality perovskite films with low defect densities. Importantly, we established for the first time the relationship between perovskite colloid charge and substrate surface charge. As a result, we achieved a power conversion efficiency (PCE) of 24.50% for FAPbI 3 -based perovskite solar cells (PSCs) under 1 SUN conditions, and a 39.01% indoor PCE for 1.67 eV wide-bandgap-based PSCs under 1000 lx LED illumination. Our findings provide critical insights into colloidal–substrate interactions, offering guidance for the development of high-performance PSCs suitable for both outdoor and indoor applications. This study presents colloidal engineering using surfactants to control colloidal size and charge in perovskite precursor solutions, enabling slow, homogeneous crystallization and high-quality, low-defect perovskite films. The established charge relationship between colloids and substrates advances high-performance perovskite solar cell development for diverse applications. • Surfactant-assisted colloidal engineering reduces size and reverses surface charge. • Controlled colloids lead to uniform grains and fewer defects at buried interfaces. • FAPbI 3 perovskite solar cells achieved 24.50% PCE under 1 SUN with colloid control. • Wide- E g perovskite solar cells reached 39.01% iPCE under LED 1000 lx with high V OC . • This strategy enables stable, high-efficiency PSCs across various light conditions.
Authors
- Seo‐Jin Ko (ORCID: https://orcid.org/0000-0002-7362-6149)
- Sang Uk Park (ORCID: https://orcid.org/0009-0005-7018-5746)
- Shujuan Huang (ORCID: https://orcid.org/0000-0003-3468-4773)
- Min Jun Choi
- Hye W. Chun
- Jincheol Kim (ORCID: https://orcid.org/0000-0001-7374-2740)
- Jong H. Kim (ORCID: https://orcid.org/0000-0001-6782-2154)
- Nochang Park (ORCID: https://orcid.org/0000-0001-7881-8492)
- Gyeong G. Jeon (ORCID: https://orcid.org/0000-0003-2463-1299)
- So Jeong Shin
- Sang Eun Yoon
- Jonghoon Han
Institutions
- Daegu Gyeongbuk Institute of Science and Technology (KR)
- Korea Electronics Technology Institute (KR)
- Ajou University (KR)
- Macquarie University (AU)
Publication Details
- Journal
- Chemical Engineering Journal
- Published
- 2025-06-16
- DOI
- https://doi.org/10.1016/j.cej.2025.164991
- Citations
- 2
- Primary Topic
- Perovskite Materials and Applications
- Type
- article
- Field-Weighted Citation Impact
- 1.46
Funders
- Ministry of Trade, Industry and Energy
- National Research Foundation of Korea
- Ministry of Science and ICT, South Korea
- Australian Research Council
- Korea Institute of Energy Technology Evaluation and Planning