Local Charge Distribution Engineered by Schottky Heterojunctions toward Urea Electrolysis

Urea electrooxidation with favorable thermodynamic potential offers great promise for decoupling H₂/O₂ evolution from sluggish water splitting, and simultaneously mitigating the problem of urea‐rich water pollution. However, the intrinsically slow kinetics of the six‐electron transfer process impels one to explore efficient catalysts in order to enable widespread use of this catalytic system. In response, taking CoS₂/MoS₂ Schottky heterojunctions as the proof‐of‐concept paradigm, a catalytic model to modulate the surface charge distribution for synergistically facilitating the adsorption and fracture of chemical group in urea molecule is proposed and the mechanism of urea electrooxidation at the molecular level is elucidated. Based on density functional calculations, the self‐driven charge transfer across CoS₂/MoS₂ heterointerface would induce the formation of local electrophilic/nucleophilic region, which will intelligently adsorb electron‐donating/electron‐withdrawing groups in urea molecule, activate the chemical bonds, and thus trigger the decomposition of urea. Benefiting from the regulation of local charge distribution, the constructed Schottky catalyst of CoS₂‐MoS₂ exhibits superior urea catalytic activities with a potential of 1.29 V (only 0.06 V higher than the thermodynamic voltage of water decomposition) to attain 10 mA cm^?2 as well as robust durability over 60 h. This innovational manipulation of charge distribution via Schottky heterojunction provides a model in exploring other highly efficient electrocatalysts.