纳米片
化学
六价铬
催化作用
电子转移
密度泛函理论
铬
纳米颗粒
化学工程
氧化还原
热解
甲酸
纳米技术
光化学
无机化学
计算化学
有机化学
材料科学
工程类
作者
Lixia Wang,Rongfei Ye,Panming Jian,Jie Shi,Jiangyong Liu
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-02-20
卷期号:63 (9): 4214-4223
被引量:12
标识
DOI:10.1021/acs.inorgchem.3c04320
摘要
The reductive transformation of Cr(VI) into Cr(III) mediated by formic acid with efficient, stable, and cost-effective catalysts is a promising strategy for remediating Cr(VI) contamination. Herein, we report the facile construction of uniform Co@NC nanosheet-assembled microflowers for the reduction of Cr(VI). Both experimental results and density functional theory (DFT) calculations reveal the vital role of the intensive interfacial electronic interaction between Co nanoparticles and the N-doped carbon layer in facilitating the anchoring and dispersion of Co nanoparticles within the carbon framework. The interfacial electron transfer from Co to NC contributes to the interaction with Cr2O72– ions, promoting the subsequent H-transfer reaction. A Langmuir–Hinshelwood kinetic model has been established for the Cr(VI) reduction catalyzed by the CNCF2 (pyrolyzed at 700 °C), which shows a superior reaction performance. This study provides a facile strategy to delicately design well-assembled heterostructures with rich interfaces and strong interfacial interactions for a series of applications in environmental/thermal catalysis.
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