Intrinsic Effects of Sulfidation on the Reactivity of Zero-Valent Iron With Trichloroethene: A DFT Study

Abstract

Sulfidation represents a promising approach to enhance the selectivity and longevity of zero-valent iron (ZVI) in water treatment, particularly for nanoscale ZVI (nZVI). While previous mechanistic studies have primarily concentrated on the impact of sulfidation on the (n)ZVI hydrophobicity, the fundamental effects of sulfidation on the (n)ZVI reactivity with target contaminants remain poorly understood. Herein, we employed density functional theory to elucidate reaction mechanisms of trichloroethene (TCE) dechlorination at various (n)ZVI surface models, ranging from pristine Fe ⁰ to regularly sulfidated Fe surfaces. Our findings indicate that sulfidation intrinsically hinders the TCE dechlorination by (n)ZVI, which aligns with prior observations of sulfur poisoning in transition metal catalysts. We further demonstrate that the positive effects of sulfidation emerge when the surface of (n)ZVI undergoes corrosion. Notably, S sites exhibit higher reactivity compared to the sites typically present on the surface of (n)ZVI oxidized in water. Additionally, S sites protect nearby Fe sites against oxidation and make them more selective for direct electron transfer. Overall, our results reveal that the reactivity of sulfidated (n)ZVI is governed by an interplay of intrinsic inhibitory effects and corrosion protection. A deeper understanding of these phenomena may provide new insights into the selectivity of sulfidated (n)ZVI for specific contaminants.