Title

Regulating Crystal Facets of MnO2 for Enhancing Peroxymonosulfate Activation to Degrade Pollutants: Performance and Mechanism

Publication Name

Catalysts

Abstract

On the catalyst surface, crystal facets with different surface atom arrangements and diverse physicochemical properties lead to distinct catalytic activity. Acquiring a highly reactive facet through surface regulation is an efficient strategy to promote the oxidative decomposition of wastewater organic pollutants via peroxymonosulfate (PMS) activation. However, the mechanism through which crystal facets affect PMS activation is still unclear. In this study, three facet-engineered α-MnO2 with different exposed facets were prepared via a facile hydrothermal route. The prepared 310-MnO2 exhibited superior PMS activation performance to 100-MnO2 and 110-MnO2. Moreover, the 310-MnO2/PMS oxidative system was active over a wide pH range and highly resistant to interfering substances from wastewater. These advantages of the 310-MnO2/PMS system make it highly promising for practical wastewater treatment. Based on quenching experiments, electron paramagnetic resonance (EPR) analysis, solvent exchange, and electrochemical measurements, mediated electron transfer was found to be the dominant nonradical pathway for p-chloroaniline (PCA) degradation. A sulfhydryl group (-SH) masking experiment showed that the highly exposed Mn atoms on the 310-MnO2 surface were sites of PMS activation. In addition, density functional theory (DFT) calculations confirmed that the dominant {310} facet promoted adsorption/activation of PMS, which favored the formation of more metastable complexes on the α-MnO2 surface. The reaction mechanism obtained here clarifies the relationship between PMS activation and crystal facets. This study provides significant insights into the rational design of high-performance catalysts for efficient water remediation.

Open Access Status

This publication may be available as open access

Volume

12

Issue

3

Article Number

342

Funding Number

201804010398

Funding Sponsor

National Natural Science Foundation of China

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Link to publisher version (DOI)

http://dx.doi.org/10.3390/catal12030342