Junzhi Ye, Charlie Nicholls, Woo Hyeon Jeong, Dong Yoon Chung, Ashish Gaurav, Kieran De-Ville, Rui Xu, Zongming Ni, Qingyu Wang, Xinyu Shen, Jieling Tan, Eilidh L. Quinn, Maxime Atkinson, Wei Zhang, Haitao Zhao, Henry J. Snaith, Robert A. Taylor, Yunwei Zhang, Robert L. Z. Hoye
High Resolution Image Download MS PowerPoint Slide Lead-halide perovskite nanocrystals (NCs) have gained attention for optoelectronics, but careful selection of the antisolvent used for purification is essential to achieve high monodispersity and yield while minimizing surface damage. Current understanding indicates that this requires lowering the relative polarity of the antisolvent, yet high-polarity antisolvents are widely used for purification, as we confirm through data mining. We show that polarity alone is insufficient for antisolvent selection by comparing ethyl acetate and acetonitrile for CsPbI 3 NC purification. Despite its higher polarity, acetonitrile yields improved colloidal stability compared to ethyl acetate. Using 1 H NMR, FTIR, and XPS measurements, alongside DFT calculations, we demonstrate that acetonitrile acts as a stronger Lewis base, binding to and passivating the NC surface. Coordination of acetonitrile to the perovskite NC surface enhances stability and improves their performance in light-emitting diodes. These findings establish a mechanistic framework for antisolvent selection to realize bright and stable halide perovskite NCs.