Abstract

It is crucial for the photovoltaic (PV) industry to establish a circular materials flow for more sustainable solar silicon production. In the present work, a series of K2O-SiO2 and K2O-CaO-SiO2 slags were examined for the combination of silicon purification and Si-kerf waste recycling. The study revealed that the predominant mass transfer mechanism and the variation in slag composition during refining are due to the silicothermic reduction of K2O. The boron removal degree reached levels above 80% in most of tests, with boron gasification as potassium metaborate confirmed as an important mechanism for boron removal, especially in slags with high K2O content. In the case of ternary slags, the results indicated that an increase in CaO enhances boron partitioning in slag phase and a high K2O content also led to boron accumulation in the slag phase due to rapid reaction kinetics in the early stage of refining. The distinct behaviours of calcium and postassium ions in the slag phase were revealed by molecular dynamics simulations. It was found that potassium ions preferentially modify bridging oxygen, while calcium ions contribute more to depolymerizing the tectosilicate network and generating more non-bridging oxygens, which may further aid in the boron stabilization in slag phase. The oxidation layer of Si-kerf was removed successfully and enabled the coalescence of the silicon nanoparticles into the Si melt. Additionally, the presence of SiC clusters in the slag phase was also observed, indicating effective removal of SiC and the feasibility of Si-kerf waste recycling.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call