All-inorganic perovskite is a promising candidate for solar cell applications. However, a significant challenge lies in its poor phase stability to environmental moisture. To address this problem, we develop a strategy for in-situ reconstruction of the CsPbI3 3 surface using siloxane surfactants such as 3-aminopropyltriethoxysilane (APTES) and 3-aminopropyltrimethoxysilane (APTMS), which both demonstrate multifunctional roles in surface engineering. The siloxanes undergo air-induced hydrolysis, leading to the formation of Si-O-Si networks. Additionally, the -NH2 2 convert to -NH3+, 3 + , enabling interaction with the I-- ions on the surface of CsPbI3. 3 . This facilitates the formation of a self-assembled siloxane cross-linked ligand layer, which offers extra function for providing water and oxygen shielding, consequently stabilizing the surface of CsPbI3. 3 . Furthermore, the siloxane surfactants can passivate uncoordinated Pb2+ 2+ ions, resulting in a reduction of non-radiative recombination at the interface, thereby significantly augmenting device performance and stability. Following research comparisons, APTES with longer alkyl chains displays superior performance. As a result, with the APTES passivation, the PCE is increased from 19.01 % to 21.42 %, which is one of the highest PCE devices in pure CsPbI3 3 PSCs reported so far. Meanwhile, the devices treated with APTES show superior moisture stability over those without APTES, especially in the absence of encapsulation.