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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
来源:
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.
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页数:12
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