Fatma Aras, Ulrich Burkhardt, Alim Ormeci, Horst Borrmann, Simone G Altendorf, Yuri Grin, Iryna Antonyshyn
{"title":"Chemical Behavior of Mo<sub>2</sub> <i>TM</i>B<sub>2</sub> (<i>TM</i> = Fe, Co, Ni) upon the Oxygen Evolution Reaction (OER).","authors":"Fatma Aras, Ulrich Burkhardt, Alim Ormeci, Horst Borrmann, Simone G Altendorf, Yuri Grin, Iryna Antonyshyn","doi":"10.1021/acsmaterialsau.5c00035","DOIUrl":null,"url":null,"abstract":"<p><p>The (electro)-chemical behavior of intermetallic compounds Mo<sub>2</sub> <i>TM</i>B<sub>2</sub> (<i>TM</i> = Fe, Co, Ni) under OER conditions has been investigated using electrochemical data combined with extensive bulk- and surface-sensitive material characterization. <i>In situ</i> formation of <i>TM</i>-rich amorphous layers, composed of oxides and hydroxides, accompanied by partial dissolution of molybdenum and boron, was observed for all three compounds. The degree of molybdenum and boron dissolution also influences the electronic state of <i>TM</i>s in their oxides/hydroxides formed on the surface of Mo<sub>2</sub> <i>TM</i>B<sub>2</sub>. The <i>in situ</i>-formed Fe<sub>2</sub>O<sub>3</sub> and Ni-(OH)<sub>2</sub> on the surface of Mo<sub>2</sub>FeB<sub>2</sub> and Mo<sub>2</sub>NiB<sub>2</sub>, respectively, are the origin of surface passivation and their OER inactivity. At the same time, the simultaneous presence of Co<sub>3</sub>O<sub>4</sub> and Co-(OH)<sub>2</sub> on the surface of an OER-exposed Mo<sub>2</sub>CoB<sub>2</sub> electrode allows for the start of OER at a lower overpotential (ca. 290 mV) compared to elemental Co (ca. 370 mV), revealing better electrocatalytic activity. Extensive characterization of these materials as well as variation of the experimental conditions extends our understanding of the chemical properties of intermetallic compounds, which are of clear importance for their possible application as efficient electrocatalysts.</p>","PeriodicalId":29798,"journal":{"name":"ACS Materials Au","volume":"5 4","pages":"718-731"},"PeriodicalIF":6.5000,"publicationDate":"2025-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12257420/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Materials Au","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/acsmaterialsau.5c00035","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/9 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The (electro)-chemical behavior of intermetallic compounds Mo2TMB2 (TM = Fe, Co, Ni) under OER conditions has been investigated using electrochemical data combined with extensive bulk- and surface-sensitive material characterization. In situ formation of TM-rich amorphous layers, composed of oxides and hydroxides, accompanied by partial dissolution of molybdenum and boron, was observed for all three compounds. The degree of molybdenum and boron dissolution also influences the electronic state of TMs in their oxides/hydroxides formed on the surface of Mo2TMB2. The in situ-formed Fe2O3 and Ni-(OH)2 on the surface of Mo2FeB2 and Mo2NiB2, respectively, are the origin of surface passivation and their OER inactivity. At the same time, the simultaneous presence of Co3O4 and Co-(OH)2 on the surface of an OER-exposed Mo2CoB2 electrode allows for the start of OER at a lower overpotential (ca. 290 mV) compared to elemental Co (ca. 370 mV), revealing better electrocatalytic activity. Extensive characterization of these materials as well as variation of the experimental conditions extends our understanding of the chemical properties of intermetallic compounds, which are of clear importance for their possible application as efficient electrocatalysts.
期刊介绍:
ACS Materials Au is an open access journal publishing letters articles reviews and perspectives describing high-quality research at the forefront of fundamental and applied research and at the interface between materials and other disciplines such as chemistry engineering and biology. Papers that showcase multidisciplinary and innovative materials research addressing global challenges are especially welcome. Areas of interest include but are not limited to:Design synthesis characterization and evaluation of forefront and emerging materialsUnderstanding structure property performance relationships and their underlying mechanismsDevelopment of materials for energy environmental biomedical electronic and catalytic applications