Ruijing Wang, De Zhang, Sijia Luo, Lijuan Jiang, Qunlong Wang, Linlin Chen, Guang-Feng Wei, Xuefeng Wang
{"title":"The engineered interfacial Pd-O-Ti sites on the TiO2 nanobelts to accelerate water dissociation for the alkaline hydrogen evolution","authors":"Ruijing Wang, De Zhang, Sijia Luo, Lijuan Jiang, Qunlong Wang, Linlin Chen, Guang-Feng Wei, Xuefeng Wang","doi":"10.1016/j.electacta.2024.145198","DOIUrl":null,"url":null,"abstract":"Electrochemical water splitting derived by the renewable electricity is one attractive route to produce the green hydrogen. The hydrogen evolution reaction (HER) at the cathode side under the alkaline condition is relatively difficult compared with the acidic, because there is a rate-determining step of breaking strong H-OH bonding in the water molecular. Herein, the ultrafine Pd nanoparticles are uniformly distributed on the TiO<sub>2</sub> nanobelts (Pd<sub>NPs</sub>/TiO<sub>2</sub>) by the pulsed laser deposition to expose the abundant interfacial sites, showing a lower HER overpotential of 71 mV at the current density of -10 mA cm<sup>-2</sup> in 1 M KOH. The interfacial Pd-O-Ti structure on Pd<sub>NPs</sub>/TiO<sub>2</sub> provides the direct contact between active phase and the water molecules, contributing to break H-OH bond. At the same time, a selective adsorption of H on Pd and OH intermediate on TiO<sub>2</sub> is achieved in the interfacial Pd-O-Ti sites under the alkaline HER, optimizing the whole catalytic dynamic.","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":null,"pages":null},"PeriodicalIF":5.5000,"publicationDate":"2024-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.electacta.2024.145198","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Electrochemical water splitting derived by the renewable electricity is one attractive route to produce the green hydrogen. The hydrogen evolution reaction (HER) at the cathode side under the alkaline condition is relatively difficult compared with the acidic, because there is a rate-determining step of breaking strong H-OH bonding in the water molecular. Herein, the ultrafine Pd nanoparticles are uniformly distributed on the TiO2 nanobelts (PdNPs/TiO2) by the pulsed laser deposition to expose the abundant interfacial sites, showing a lower HER overpotential of 71 mV at the current density of -10 mA cm-2 in 1 M KOH. The interfacial Pd-O-Ti structure on PdNPs/TiO2 provides the direct contact between active phase and the water molecules, contributing to break H-OH bond. At the same time, a selective adsorption of H on Pd and OH intermediate on TiO2 is achieved in the interfacial Pd-O-Ti sites under the alkaline HER, optimizing the whole catalytic dynamic.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.