{"title":"Amorphous/Crystalline ZrO2 with Oxygen Vacancies Anchored Nano‐Ru Enhance Reverse Hydrogen Spillover in Alkaline Hydrogen Evolution","authors":"Jidong Niu, Huimei Duan, Tanxu Sun, Zhenhai Zhi, Daohao Li, Xiaokun Fan, Lijie Zhang, Dongjiang Yang","doi":"10.1002/smll.202410436","DOIUrl":null,"url":null,"abstract":"Hydrogen spillover‐based binary (HSBB) system has attracted significant attention in alkaline hydrogen evolution reaction (HER). Accelerating hydrogen spillover in the HSBB system is crucial for the HER activity. Herein, a highly efficient HSBB system is developed by anchoring nano‐Ru on oxygen vacancy (Vo) rich amorphous/crystal ZrO<jats:sub>2</jats:sub>. Theoretical and experimental results reveal that the water molecules dissociate on the Vo of ZrO<jats:sub>2</jats:sub> into protons, which then couple with electrons to form H<jats:sup>*</jats:sup>, and the produced H<jats:sup>*</jats:sup> are spilled over to the nano‐Ru to evolve H<jats:sub>2</jats:sub>. The amorphous regions enhance the adsorption and desorption rates of hydrogen while exposing a greater number of active sites; meanwhile, the Vo significantly reduce the work function of ZrO<jats:sub>2</jats:sub>, facilitates electron transfer from ZrO<jats:sub>2</jats:sub> to Ru, and thereby accelerates hydrogen spillover. As a result, the Ru/ac‐ZrO<jats:sub>2</jats:sub> delivers a low overpotential of 14 mV at 10 mA cm<jats:sup>−2</jats:sup> and a high mass activity of 46.47 A mg<jats:sub>metal</jats:sub><jats:sup>−2</jats:sup> at 300 mV for alkaline HER, bypass those of commercial Pt/C (19 mV and 0.09 A mg<jats:sub>metal</jats:sub><jats:sup>−2</jats:sup>, respectively).","PeriodicalId":228,"journal":{"name":"Small","volume":"48 1","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/smll.202410436","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Hydrogen spillover‐based binary (HSBB) system has attracted significant attention in alkaline hydrogen evolution reaction (HER). Accelerating hydrogen spillover in the HSBB system is crucial for the HER activity. Herein, a highly efficient HSBB system is developed by anchoring nano‐Ru on oxygen vacancy (Vo) rich amorphous/crystal ZrO2. Theoretical and experimental results reveal that the water molecules dissociate on the Vo of ZrO2 into protons, which then couple with electrons to form H*, and the produced H* are spilled over to the nano‐Ru to evolve H2. The amorphous regions enhance the adsorption and desorption rates of hydrogen while exposing a greater number of active sites; meanwhile, the Vo significantly reduce the work function of ZrO2, facilitates electron transfer from ZrO2 to Ru, and thereby accelerates hydrogen spillover. As a result, the Ru/ac‐ZrO2 delivers a low overpotential of 14 mV at 10 mA cm−2 and a high mass activity of 46.47 A mgmetal−2 at 300 mV for alkaline HER, bypass those of commercial Pt/C (19 mV and 0.09 A mgmetal−2, respectively).
氢溢出基二元体系(HSBB)在碱性析氢反应(HER)中引起了广泛的关注。加速HSBB系统中的氢气溢出对HER活性至关重要。本文通过将纳米钌锚定在富氧空位(Vo)的非晶/晶体ZrO2上,开发了一种高效的HSBB系统。理论和实验结果表明,水分子在ZrO2的Vo上解离成质子,然后与电子偶联形成H*,产生的H*溢出到纳米钌上生成H2。无定形区提高了氢的吸附和解吸速率,同时暴露出更多的活性位点;同时,Vo显著降低了ZrO2的功函数,促进了电子从ZrO2向Ru的转移,从而加速了氢的溢出。结果表明,Ru/ac‐ZrO2在10 mA cm−2条件下具有14 mV的过电位,在300 mV条件下具有46.47 a mgmetal−2的高质量活度,超过了商业Pt/C(分别为19 mV和0.09 a mgmetal−2)。
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