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Interfacial properties between passivation molecules and perovskite surface determine passivation effects on the performance and stability of perovskite solar cells. [Display omitted] • Passivation effect is related to binding strength and probability. • Strong polarity of 2-MP enhances charge separation and adsorption capacity. • 2-MP passivation improves carrier transfer capability. • 2-MP passivation leads to large bandgap. • AIMD simulations reveal water blocking effects of 2-MP, Py, and PTT. Chemical passivation implemented by Lewis base has been demonstrated as an effective method to overcome the water vulnerability of perovskite solar cells (PSCs) along with better performance. Comprehensive understanding of the surface passivation effects is crucial to future improve the PSCs efficiency and stability. Herein, we utilized first-principles to simulate the structure and electronic properties of the passivated perovskite, and carried out ab initio molecular dynamics (AIMD) to understand the effectiveness of the experimental passivation molecules, 2-MP , Py , and PTT , on the classical perovskite (Zhu et al., 2019). Calculations show that introducing both -SH and the N atom of 2-MP enhances the electric dipole moment, the binding strength, the adsorption probability and the carrier transfer rate compared to these of Py and PTT. Moreover, the efficient separation of electrons and holes at the interface and the large bandgap can be achieved by the 2-MP treatment, which is beneficial to improve the photovoltaic performance. AIMD simulations indicate that the interactions of N⋯Pb, S⋯Pb, and H⋯I between 2-MP and the MAPbI 3 surface lead to a stronger passivation effect than that of Py and PTT , which is in agreement with the experimental observations. Our results are expected to provide new ideas for developing more distinguished passivation molecules to endow the PSCs stability against water. [ABSTRACT FROM AUTHOR]

The excellent catalytic activity of [N 2,2,2,2OH ][SA] is traced to the critical role played by nucleophilic-electrophilic dual activation from [SA]- anions in the cycloaddition reaction of CO 2. [Display omitted] • The catalytic mechanism of carboxylate anion-based ionic liquids is firstly elucidated in this work. • The catalytic role of carboxylate anions is complex and flexible. • The underlying electrophilic activation ability of the carboxylic acid anion plays a critical role in enhancing the catalytic activity. • The electrophilic activation plays a more important role than nucleophilic activation in the ring-opening step. Elucidating the mechanism of carbon dioxide (CO 2) cycloaddition reaction catalyzed by ionic liquid (ILs) facilitates the rational design of efficient IL catalysts at the molecular level. To date, a great deal of research has been devoted to the halogen-containing ILs, however, the catalytic mechanism of halogen-free ILs remains unclear. In this contribution, an exhaustive theoretical study of the coupling reaction of CO 2 with epichlorohydrin (ECH) catalyzed by three halogen-free ILs has been carried out for the first time by combining density functional theory (DFT) calculations with molecular dynamics (MD) simulations. Meanwhile, the effect of carboxylate anion structure on catalytic activity is deeply investigated. The final results provide a comprehensive catalytic mechanism of carboxylate anion-based ILs. The most favorable mechanism involves three steps, i.e., ring-opening of ECH, CO 2 insertion, and ring-closure to form the product. Among them, the ring-opening of ECH is the rate-determining step (RDS). Additionally, the analytical results of the independent gradient model based on Hirshfeld partition (IGMH) and atoms in molecules (AIM) suggest that the electrophilic activation from carboxylate anions plays a critical role in promoting the ECH ring-opening process. The electrophilic activation of anions is investigated for the first time in this work. The results indicate that incorporating electrophilic groups into anions is a promising pathway to develop new robust and efficient halogen-free ILs. [ABSTRACT FROM AUTHOR]