TY - JOUR
T1 - Millisecond self-heating and quenching synthesis of Fe/carbon nanocomposite for superior reductive remediation
AU - Sun, Liming
AU - Wu, Xuan
AU - Jiao, Yubing
AU - Jia, Chao
AU - Teng, Tao
AU - Lin, Litao
AU - Yu, Fengbo
AU - He, Zhelin
AU - Gao, Jie
AU - Yan, Shuwen
AU - Shi, Guosheng
AU - Ren, Zhiyong Jason
AU - Yang, Jinguang
AU - Zhang, Shicheng
AU - Zhu, Xiangdong
N1 - Publisher Copyright: © 2023 Elsevier B.V.
PY - 2024/3
Y1 - 2024/3
N2 - Fe0-based nanomaterials are extensively applied in environmental remediation, but their passivated oxide shell restricts deep application. However, efforts aimed at revitalizing Fe-oxide shells have shown limited success. Here, we report a “faster win fast” approach by preferential carbon layer deposition in milliseconds to block Fe-oxide shell growth via carbon-assisted flash Joule heating (C-FJH) reaction. C-FJH induced ultra-high temperature and electric shock promoted reductive Fe formation and subsequently melted to a phase-fusional heterostructure (Fe0/FeCl2). Therefore, theoretical calculation confirmed that electron delocalization effect of derived heterostructure promoted electron transfer. Synchronously, rapid self-heating/quenching rate (∼102 K/ms) realized a thin aromatic-carbon layer deposition to sustain both high stability and activity of reductive Fe. The channels of thin aromatic-carbon layer favored inward diffusion of pollutants, which facilitated the subsequent reduction. Accordingly, derived heterostructure and carbon layer jointly contributed to the boosted removal of multiple pollutants (including metal oxyanions, perfluorinated compounds, and disinfection by-products).
AB - Fe0-based nanomaterials are extensively applied in environmental remediation, but their passivated oxide shell restricts deep application. However, efforts aimed at revitalizing Fe-oxide shells have shown limited success. Here, we report a “faster win fast” approach by preferential carbon layer deposition in milliseconds to block Fe-oxide shell growth via carbon-assisted flash Joule heating (C-FJH) reaction. C-FJH induced ultra-high temperature and electric shock promoted reductive Fe formation and subsequently melted to a phase-fusional heterostructure (Fe0/FeCl2). Therefore, theoretical calculation confirmed that electron delocalization effect of derived heterostructure promoted electron transfer. Synchronously, rapid self-heating/quenching rate (∼102 K/ms) realized a thin aromatic-carbon layer deposition to sustain both high stability and activity of reductive Fe. The channels of thin aromatic-carbon layer favored inward diffusion of pollutants, which facilitated the subsequent reduction. Accordingly, derived heterostructure and carbon layer jointly contributed to the boosted removal of multiple pollutants (including metal oxyanions, perfluorinated compounds, and disinfection by-products).
KW - Environmental remediation
KW - Fe-based nanomaterials
KW - Flash Joule heating
KW - Oxide shell-free
KW - Reduction
UR - http://www.scopus.com/inward/record.url?scp=85174192216&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85174192216&partnerID=8YFLogxK
U2 - 10.1016/j.apcatb.2023.123361
DO - 10.1016/j.apcatb.2023.123361
M3 - Article
SN - 0926-3373
VL - 342
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
M1 - 123361
ER -