Theoretical insight into mercury species adsorption on graphene-based Pt single-atom catalysts

Wenchao Ji; Xiuhua Xiao; Feiyue Li; Xingjun Fan; Yuanyuan Meng; Maohong Fan

doi:10.1039/d1ra08891b

Theoretical insight into mercury species adsorption on graphene-based Pt single-atom catalysts

RSC Adv. 2022 Feb 16;12(10):5797-5806. doi: 10.1039/d1ra08891b.

Authors

Wenchao Ji¹, Xiuhua Xiao¹, Feiyue Li¹, Xingjun Fan¹, Yuanyuan Meng², Maohong Fan³

Affiliations

¹ College of Resource and Environment, Anhui Science and Technology University Fengyang 233100 China.
² College of Chemistry & Chemical Engineering, Taiyuan University of Technology Taiyuan 030024 P. R. China mengyuanyuan@tyut.edu.cn.
³ Departments of Chemical and Petroleum Engineering, University of Wyoming Laramie WY 82071 USA mfan@uwyo.edu.

Abstract

Mercury emission from coal-fired flue gases is environmentally crucial. Revealing the interaction between mercury (Hg) and functional materials is significant to controlling emission. We conducted an investigation into the adsorption mechanism of mercury species onto graphene-based Platinum (Pt) single-atom catalysts (SACs). Single-atom Pt is the active center for Hg species chemisorption, with an adsorption energy range of 0.555-3.792 eV. In addition, Hg species adsorbed preferentially at lower temperatures. Pt/3N-GN exhibits a higher adsorption ability than Pt/SV-GN. The strong interaction of Hg⁰ with Pt SACs contributed to atomic-orbital hybridization between them. Further analysis revealed that s, p orbitals of Hg contribute significantly to orbital hybridization with Pt SACs. Moreover, the charge decomposition analysis confirmed that s, p orbitals of Hg hybridized with d, s orbitals of Pt SACs. The net charge transfer from Hg⁰ to Pt/SV-GN and Pt/3N-GN are 0.059 and 0.097 e^-, respectively. The higher the charge transfers, the more intense the electron and orbital interaction between Hg and the surface. Consequently, Pt/3N-GN is a highly effective catalyst for Hg adsorption.