In Situ Probing the Structure Change and Interaction of Interfacial Water and Hydroxyl Intermediates on Ni(OH) 2 Surface over Water Splitting.

There is growing acknowledgment that the properties of the electrochemical interfaces play an increasingly pivotal role in improving the performance of the hydrogen evolution reaction (HER). Here, we present, for the first time, direct dynamic spectral evidence illustrating the impact of the interaction between interfacial water molecules and adsorbed hydroxyl species (OH ad ) on the HER properties of Ni(OH) 2 using Au/core-Ni(OH) 2 /shell nanoparticle-enhanced Raman spectroscopy. Notably, our findings highlight that the interaction between OH ad and interfacial water molecules promotes the formation of weakly hydrogen-bonded water, fostering an environment conducive to improving the HER performance. Furthermore, the participation of OH ad in the reaction is substantiated by the observed deprotonation step of Au@2 nm Ni(OH) 2 during the HER process. This phenomenon is corroborated by the phase transition of Ni(OH) 2 to NiO, as verified through Raman and X-ray photoelectron spectroscopy. The significant redshift in the OH-stretching frequency of water molecules during the phase transition confirms that surface OH ad disrupts the hydrogen-bond network of interfacial water molecules. Through manipulation of the shell thickness of Au@Ni(OH) 2 , we additionally validate the interaction between OH ad and interfacial water molecules. In summary, our insights emphasize the potential of electrochemical interfacial engineering as a potent approach to enhance electrocatalytic performance.