Reactant enrichment in yolk-shell structured Pd/TiN nanoreactors for boosting electrocatalytic hydrodechlorination performance

纳米反应器 催化作用 化学工程 纳米材料基催化剂 材料科学 介孔材料 金属 吸附 纳米技术 化学 纳米颗粒 有机化学 冶金 工程类
作者
Zhang Jun,Chunyuan Wang,Shiyu Lu,Shuyue Liu,Pingjuan Liang,Huan Yi,Mengjie Li,Jin Meng,Rong Wang,Guangming Jiang
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:481: 148325-148325 被引量:5
标识
DOI:10.1016/j.cej.2023.148325
摘要

Enhancing the enrichment behavior of low-concentration chlorinated organic pollutants remains a significant challenge in electrocatalytic hydrodechlorination (EHDC) technology. Metal-loaded hollow nanoarchitecture has emerged as a promising nanoreactor to improve reaction enrichment behavior because of its tailorable microenvironments and electronic properties. Herein, a structural engineering strategy is developed to synthesize yolk-shell structured TiN spheres supported Pd nanoreactors (Pd/YS-TiN) with confined mesoscopic spaces. Characterization by multiple techniques reveals that the yolk-shell structure of YS-TiN, with high specific surface area (139.0 m2/g) and appropriately mesoporosity (6.9 nm), exposes numerous Pd nanoparticles (∼4.0 nm) on outer/inner surface of the shell and yolk-core solid sphere, ensuring an efficient utilization of active sites for enhancing the 2,4-DCP detoxification. Consequently, the structurally optimized Pd/YS-TiN nanoreactor consistently displays maximum reaction kinetics, dechlorination degree, faradaic current density, H* utilization and product selectivity, surpassing hollow TiN-supported Pd and Pd/C catalysts. The super EHDC performance of 91.8 % 2,4-DCP conversion, a specific activity of 1.68 min−1 molPd−1, and a mass activity of 6.06 min−1 gPd−1 is obtained at −0.85 V and 180 min, outperforming most reported catalysts. Combining experimental and density functional theory results, the exceptional reaction enrichment behavior of Pd/YS-TiN originates from (1) alleviating the overstrong adsorption of product phenol through strong metal-support interactions and (2) enhancing mass transport efficiency facilitated by the local concentration gradient and mesoporous shell. This study elucidates how metal-support interactions and mass transport synergistically enhance reaction enrichment behavior, showcasing potential benefits in environmental remediation applications.
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