Li Gong,Jingting Chen,Guangming Zhan,Junning Zu,Hao Li,Feng He,Paul G. Tratnyek,Lizhi Zhang
The widespread application of zerovalent iron (ZVI) in water treatment and remediation has motivated research into modifications of the material that result in improved performance. The newest and most promising involves nitridation, but available methods for nitridation are not environmentally sustainable processes. Here, we demonstrate that mechanochemical molten-salt-assisted synthesis can be an effective method to produce surface-nitridated ZVI (sN-ZVI). This modification promoted the dechlorination rate of ZVI by up to 82-fold toward chlorinated ethenes and chloroform (CF). Enhanced conductivity of the nitridated shell boosts outward electron transfer from the iron core, while the exposed iron nitrides are efficient in activating the C–Cl bond of both trichloroethene and chloroform and facilitate electron-transfer-mediated C–Cl cleavage with an energy barrier of 0.20 eV, lower than that of iron oxides (0.78 eV). More importantly, sN-ZVI minimizes side hydrogen evolution and promotes deep dechlorination, thus preventing the formation of any toxic chlorinated intermediates, even in the case of highly chlorinated carbons such as tetrachloroethene and chloroform. sN-ZVI maintains its dechlorination performance even after 100 days of water aging, highlighting its great potential for field remediation applications.
Silicon (Si), a promising high-capacity anode material for lithium-ion batteries, suffers from severe volume changes upon cycling, leading to rapid capacity fading. This study mitigates the capacity fading issue by introducing a surface SiN x layer on micron Si, which is in-situ converted into a Li x SiN y -based artificial solid electrolyte interphase (SEI). This artificial SEI not only effectively restricts SEI growth to the outmost surface, but also induces a self-optimized structural evolution of the inner Si from micron particles to nanoporous network within 20 cycles. This self-optimized nanoprous Si network exhibits low volume expansion and enhanced reaction kinetics. Consequently, the Si@SiN x /TiN demonstrates a high capacity, stable cycling, and good fast-charging capability.
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