Abstract

Novel flower-shaped C-dots/Co3O4{111} with dual-reaction centers were constructed to improve the Fenton-like reaction activity and peroxymonosulfate (PMS) conversion to sulfate radicals. Due to the exposure of a high surface area and Co3O4{111} facets, flower-shaped C-dots/Co3O4{111} could provide more Co(II) for PMS activation than traditional spherical Co3O4{110}. Meanwhile, PMS was preferred for adsorption on Co3O4{111} facets because of a high adsorption energy and thereby facilitated the electron transfer from Co(II) to PMS. More importantly, the Co–O–C linkage between C-dots and Co3O4{111} induced the formation of the dual-reaction center, which promoted the production of reactive organic radicals (R•). PMS could be directly reduced to SO4−• by R• over C-dots. On the other hand, electron transferred from R• to Co via Co–O–C linkage could accelerate the redox of Co(II)/(III), avoiding the invalid decomposition of PMS. Thus, C-dots doped on Co3O4{111} improved the PMS conversion rate to SO4−• over the single active site, resulting in high turnover numbers (TONs). In addition, TPR analysis indicated that the optimal content of C-dots doped on Co3O4{111} is 2.5%. More than 99% of antibiotics and dyes were degraded over C-dots/Co3O4{111} within 10 min. Even after six cycles, C-dots/Co3O4{111} still remained a high catalytic activity.

Highlights

  • Introduction published maps and institutional affilBeing attributed to higher oxidative potential (E0 = 2.5–3.1 V) and longer half-life (t1/2 = 30–40 μs), sulfate radical (SO4 − ) could degrade organics more efficiently thanOH (E0 = 2.80 V, t1/2 =

  • Co3 O4 synthesized by hydrothermal reaction without CTMAB are spherical particles with the diameter of 2 μm (Figure 1a)

  • We propose that Co–O–C bonds conjugated in flower-shaped carbon quantum dots (C-dots)/Co3 O4 {111} facilitate electron transfer and correlate well with the transformation from R to R

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Summary

Introduction

Introduction published maps and institutional affilBeing attributed to higher oxidative potential (E0 = 2.5–3.1 V) and longer half-life (t1/2 = 30–40 μs), sulfate radical (SO4 − •) could degrade organics more efficiently thanOH• (E0 = 2.80 V, t1/2 =

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