Surface reconstruction enabling MoO2/MoP hybrid for efficient electrocatalytic oxidation of p-xylene to terephthalic acid

被引:15
|
作者
Lv, Ye [1 ]
Peng, Mao [1 ,2 ]
Yang, Weiwei [1 ]
Liu, Menghui [1 ]
Kong, Aiqun [3 ]
Fu, Yan [1 ]
Li, Wei [1 ]
Zhang, Jinli [1 ,3 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300350, Peoples R China
[2] Tianjin Univ, Inst Shaoxing, Tianjin 312300, Zhejiang, Peoples R China
[3] Shihezi Univ, Sch Chem & Chem Engn, State Key Lab Incubat Base Green Proc Chem Engn, Shihezi 832003, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrocatalytic oxidation; p-Xylene; Transition metal phosphide; Surface reconstruction; Terephthalic acid; OXYGENATION;
D O I
10.1016/j.apcatb.2023.123229
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Selective oxidation of p-xylene (PX) to terephthalic acid (TA) remains exceptionally challenging since it easily undergoes deep oxidation. Herein, a nickel foam-supported molybdenum dioxide/molybdenum phosphide hybrid electrocatalyst (MoO2/MoP/NF) is reported for highly selective generation of TA via electrocatalytic oxidation (ECO) of PX in alkaline medium. The efficient MoO2/MoP/NF anode material displays a unique cluster like nanocone architecture, showing abundant active sites and rapid charge transfer kinetics. Benefit from the synergy between MoO2 and MoP, the MoO2/MoP/NF provides a high TA selectivity of 94.8% and an outstanding faradaic efficiency of 76.9% at the conversion of 71.6%. Additionally, the anodic oxidation of PX over MoO2/ MoP/NF promotes the cathodic hydrogen production. The potential-induced surface reconstruction of the as synthesized MoO2/MoP/NF yields new phases of phosphomolybdate and potassium molybdate. The top P site on the phosphomolybdate surface facilitates the adsorption of reaction intermediates but weakens the adsorption of TA, thereby yielding high selectivity toward TA.
引用
收藏
页数:12
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