Charge Redistribution of Lattice‐Mismatched Co─Cu3P Boosting pH‐Universal Water/Seawater Hydrogen Evolution

Abstract Practical applications of the hydrogen evolution reaction (HER) rely on the development of highly efficient, stable, and low‐cost catalysts. Tuning the electronic structure, morphology, and architecture of catalysts is an important way to realize efficient and stable HER electrocatalysts. Herein, Co‐doped Cu 3 P‐based sugar‐gourd structures (Co─Cu 3 P/CF) are prepared on copper foam as active electrocatalysts for hydrogen evolution. This hierarchical structure facilitates fast mass transport during electrocatalysis. Notably, the introduction of Co not only induces a charge redistribution but also leads to lattice‐mismatch on the atomic scale, which creates defects and performs as additional active sites. Therefore, Co─Cu 3 P/CF requires an overpotential of only 81, 111, 185, and 230 mV to reach currents of 50, 100, 500, and 1000 mA cm −2 in alkaline media and remains stable after 10 000 CV cycles in a row and up to 110 h i–t stability tests. In addition, it also shows excellent HER performance in water/seawater electrolytes of different pH values. Experimental and DFT show that the introduction of Co modulates the electronic and energy level structures of the catalyst, optimizes the adsorption and desorption behavior of the intermediate, reduces the water dissociation energy barrier during the reaction, accelerates the Volmer step reaction, and thus improves the HER performance.