{"title":"Fluorination Anodization of n-Type Silicon in the Dark via Schottky-Driven Electron Extraction","authors":"Benjamin Tien-Hsi Lee, Chao-Chia Cheng, Chun-Huang Wu, Lin Cheng, Yu-Sheng Chiou, Shu-Cheng Li, Wei-Chi Huang, Chao-Yuan Cheng, Yang-Chun Chiu, Chao-Ching Chiang","doi":"10.1021/acsmaterialsau.6c00002","DOIUrl":null,"url":null,"abstract":"<p>The band structure of semiconductors governs electron\r\nexchange,\r\nrendering interfacial electron transfer both controllable and intrinsically\r\ntime-integrated. Because electron transfer affects the formation and\r\nrupture of interatomic bonds, it constitutes the main driving force\r\nof chemical and electrochemical reactions. Fluorination anodization\r\nof <em>n-</em>type silicon in the dark is traditionally considered\r\nimpossible because of the scarcity of the required species─holes.\r\nHere, we report that sufficiently sustained bias induces fluorination\r\nanodization of <em>n-</em>type silicon in complete darkness\r\nunder standard electrochemical conditions. We attribute this phenomenon\r\nto the formation of a Schottky junction at the metal–semiconductor\r\ncontact. Continuous long-term electron extraction through this interface\r\nguides a dynamic charge reconstruction, resulting in hole accumulation\r\nand the creation of a provisional inversion layer. Moreover, to validate\r\nthis Schottky-driven mechanism, we designed a localized laser beam\r\nwith an irradiation diameter of 1 mm using three distinct wavelengths─corresponding\r\nto energies greater than, near, and less than the silicon bandgap─as\r\na probed region during dark electrochemical processing. These experiments\r\nreveal that the anodization reaction pathway is controlled by internal\r\ncarrier redistribution, i.e., self-doped holes. We introduce an “electric-field\r\nbudget” framework to quantify the cumulative effect of electron\r\ntransfer and bias duration on electrochemical kinetics. We report\r\nthat electric-field-induced electron transfer in semiconductors─particularly\r\nits time-integrated and cumulative potential dictated by the interfacial\r\nenergy barrier─enables chemical or electrochemical reactions\r\neven without appropriate external excitation.</p>","PeriodicalId":29798,"journal":{"name":"ACS Materials Au","volume":"6 5","pages":"1077–1086"},"PeriodicalIF":9.1000,"publicationDate":"2026-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Materials Au","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsmaterialsau.6c00002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/3/27 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The band structure of semiconductors governs electron
exchange,
rendering interfacial electron transfer both controllable and intrinsically
time-integrated. Because electron transfer affects the formation and
rupture of interatomic bonds, it constitutes the main driving force
of chemical and electrochemical reactions. Fluorination anodization
of n-type silicon in the dark is traditionally considered
impossible because of the scarcity of the required species─holes.
Here, we report that sufficiently sustained bias induces fluorination
anodization of n-type silicon in complete darkness
under standard electrochemical conditions. We attribute this phenomenon
to the formation of a Schottky junction at the metal–semiconductor
contact. Continuous long-term electron extraction through this interface
guides a dynamic charge reconstruction, resulting in hole accumulation
and the creation of a provisional inversion layer. Moreover, to validate
this Schottky-driven mechanism, we designed a localized laser beam
with an irradiation diameter of 1 mm using three distinct wavelengths─corresponding
to energies greater than, near, and less than the silicon bandgap─as
a probed region during dark electrochemical processing. These experiments
reveal that the anodization reaction pathway is controlled by internal
carrier redistribution, i.e., self-doped holes. We introduce an “electric-field
budget” framework to quantify the cumulative effect of electron
transfer and bias duration on electrochemical kinetics. We report
that electric-field-induced electron transfer in semiconductors─particularly
its time-integrated and cumulative potential dictated by the interfacial
energy barrier─enables chemical or electrochemical reactions
even without appropriate external excitation.
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