Superhydrophilic Dendritic FeP/Cu3P Electrocatalyst for Urea Splitting via the Intramolecular Mechanism

被引:4
|
作者
Li, Fang [1 ]
Cao, Jing [1 ]
Yu, Huiqin [1 ]
Lin, Haili [1 ]
Chen, Shifu [1 ]
机构
[1] Huaibei Normal Univ, Coll Chem & Mat Sci, Key Lab Green & Precise Synthet Chem & Applicat, Minist Educ, Huaibei 235000, Anhui, Peoples R China
关键词
BIFUNCTIONAL ELECTROCATALYSTS; HETEROPOROUS MOS2/NI3S2; OXIDATION CATALYSIS; HYDROGEN-PRODUCTION; NI FOAM; WATER; EFFICIENT; NANOSHEETS; INTERFACE; HYDROXIDE;
D O I
10.1021/acs.inorgchem.3c04285
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The electrocatalytic overall urea splitting can achieve the dual goals of urea treatment and hydrogen energy acquisition. Herein, we exploited the principle of precipitation dissolution equilibrium to obtain bimetallic phosphide FeP/Cu3P/CF for the simultaneous oxidation of urea and reduction of water and comprehensively reveal the inherent molecular thermodynamic mechanisms on the surface of catalysts. The excellent electrochemical performance can be derived from the super water affinity and synergistic effect. Especially, the theoretical calculation unveils that the synergistic effect between FeP and Cu3P can lower the activation energy required for urea electrooxidation, thereby promoting urea splitting. In situ differential electrochemical mass spectrometry (in situ DEMS) measurements further demonstrated that urea oxidation on FeP/Cu3P/CF proceeded according to the intramolecular mechanism. This work has laid the foundation for constructing highly efficient superhydrophilic bifunctional electrocatalysts. [GRAPHICS]
引用
收藏
页码:4204 / 4213
页数:10
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