Abstract
Tuning the local reaction environment is an important and challenging issue for determining electrochemical performances. Herein, we propose a strategy of intentionally engineering the local reaction environment to yield highly active catalysts. Taking Pt(δ-) nanoparticles supported on oxygen vacancy enriched MgO nanosheets as a prototypical example, we have successfully created a local acid-like environment in the alkaline medium and achieve excellent hydrogen evolution reaction performances. The local acid-like environment is evidenced by operando Raman, synchrotron radiation infrared and X-ray absorption spectroscopy that observes a key H(3)O(+) intermediate emergence on the surface of MgO and accumulation around Pt(δ-) sites during electrocatalysis. Further analysis confirms that the critical factors of the forming the local acid-like environment include: the oxygen vacancy enriched MgO facilitates H(2)O dissociation to generate H(3)O(+) species; the F centers of MgO transfers its unpaired electrons to Pt, leading to the formation of electron-enriched Pt(δ-) species; positively charged H(3)O(+) migrates to negatively charged Pt(δ-) and accumulates around Pt(δ-) nanoparticles due to the electrostatic attraction, thus creating a local acidic environment in the alkaline medium.