Computationally guided synthesis of carbon coated mesoporous silica materials

Mesoporous silica materials (MSMs) are well -suited for biomedical applications due to their unique features, including a large surface area and tunable pore size. To enhance their durability, the small pores in MSMs are filled with carbon precursors and then carbonized to prevent them from interacting with unreacted silicic acid. In this study, we synthesized and healed MSMs using a combination of non -reactive and reactive molecular dynamics (MD) simulations. The non -reactive MD simulation revealed that the self -assembly of Pluronic (R) L64 polymers in water resulted in nearly 80 % hydrogen bonds between the hydrophilic sections of the micelle and water. In the bond -boosted ReaxFF MD simulations, silicic acid precursors were condensed on the micelle surface, with over 60 % of them leading to the creation of periodic mesoporous silica within the system. Condensation of silicic acid precursors at 300 K with bond -boosting and at 1500 K without it both significantly promoted the polymerization of Si(OH)4, with the latter doubling the rate compared to the former. Subsequently, we healed the MSM surface by carbonizing carbon precursors inside an MSM pore. Polyethylene (PE) and high -rank lignite were identified as the most suitable precursors due to their ability to form turbostratic graphene structures. High -rank lignite exhibited the highest carbon conversion ratio to 6 -membered rings, closely followed by PE, in the carbon ring formation analysis. Additionally, the production of gases, such as H2, increased significantly for PE at both 2200 K and 2600 K, indicating the conversion of a considerable portion of carbon into graphitic or turbostratic structures. The carbonization of PE primarily led to the formation of planar (sp2) structures, while sucrose yielded the least planar structures. Finally, we studied the protective blocking of unreacted silicic acid precursor by considering a PET turbostratic graphene structure in a silica mesopore formed at 2600 K. The trajectory analysis showed that the surface of the silica was effectively coated with PET tar, preventing unreacted silicic acid from interacting with the inner silica pore surface. These findings offer valuable insights into the synthesis and carbonization -based healing processes of MSMs, enhancing their potential for various biomedical applications.