TY - JOUR
T1 - Low-temperature hydrogenation of nanodiamond as a strategy to fabricate sp3-hybridized nanocarbon as a high-performance persulfate activator
AU - Gim, Gundu
AU - Haider, Zeeshan
AU - Suh, Sae In
AU - Ahn, Yong Yoon
AU - Kim, Kitae
AU - Kim, Eun Ju
AU - Lee, Hongshin
AU - Kim, Hyoung il
AU - Lee, Jaesang
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/11/5
Y1 - 2022/11/5
N2 - This study presents the first instance of the application of hydrogenated nanodiamonds (H-NDs) for persulfate activation and the associated organic degradation. Surface hydrogenation at 600 ℃, confirmed by the increased surface density of the C-H moiety in XPS and FT-IR spectra, produced H-NDs that outperformed graphitized NDs (prepared via annealing at 1000 ℃) in terms of organic degradation and persulfate utilization efficiency. Hydrogenation improved the electrical conductivity of NDs; however, it was not accompanied by an increase in the sp2 carbon content − in contrast to energy-intensive ND graphitization − resulting from sp3-to-sp2 carbon transformation. In addition to the enhanced electron-transfer mediating activity, evidenced by the negative shift of the open circuit potential and current generation, isothermal titration calorimetry measurements indicated a significantly higher binding affinity of H-ND toward persulfate compared with that of graphitized ND. Multiple empirical results confirmed the progress of electron-transfer mediation as a major activation pathway.
AB - This study presents the first instance of the application of hydrogenated nanodiamonds (H-NDs) for persulfate activation and the associated organic degradation. Surface hydrogenation at 600 ℃, confirmed by the increased surface density of the C-H moiety in XPS and FT-IR spectra, produced H-NDs that outperformed graphitized NDs (prepared via annealing at 1000 ℃) in terms of organic degradation and persulfate utilization efficiency. Hydrogenation improved the electrical conductivity of NDs; however, it was not accompanied by an increase in the sp2 carbon content − in contrast to energy-intensive ND graphitization − resulting from sp3-to-sp2 carbon transformation. In addition to the enhanced electron-transfer mediating activity, evidenced by the negative shift of the open circuit potential and current generation, isothermal titration calorimetry measurements indicated a significantly higher binding affinity of H-ND toward persulfate compared with that of graphitized ND. Multiple empirical results confirmed the progress of electron-transfer mediation as a major activation pathway.
KW - Electron-transfer mediation
KW - Nanodiamond
KW - Non-radical persulfate activation
KW - Surface binding affinity
KW - Surface hydrogenation
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U2 - 10.1016/j.apcatb.2022.121589
DO - 10.1016/j.apcatb.2022.121589
M3 - Article
AN - SCOPUS:85132236062
SN - 0926-3373
VL - 316
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
M1 - 121589
ER -