Fluorination Anodization of n-Type Silicon in the Dark via Schottky-Driven Electron Extraction

IF 9.1 Q2 CHEMISTRY, PHYSICAL
ACS Materials Au Pub Date : 2026-09-09 Epub Date: 2026-03-27 DOI:10.1021/acsmaterialsau.6c00002
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
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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.

利用肖特基驱动电子萃取法在黑暗中对n型硅进行氟化阳极氧化
半导体的能带结构控制着电子交换,使得界面电子转移既可控又具有内在的时间集成性。由于电子转移影响原子间键的形成和断裂,它构成了化学和电化学反应的主要驱动力。传统上认为,在黑暗中对n型硅进行氟化阳极氧化是不可能的,因为所需的物质──空穴十分稀缺。在这里,我们报告了在标准电化学条件下,在完全黑暗的条件下,足够持续的偏压诱导n型硅的氟化阳极氧化。我们将这一现象归因于在金属-半导体接触处形成了肖特基结。通过该界面连续的长期电子提取引导动态电荷重建,导致空穴积累和临时反转层的创建。此外,为了验证这种肖特基驱动机制,我们设计了一种局部激光束,其照射直径为1毫米,使用三种不同的波长──对应于暗电化学处理过程中探测区域的能量大于、接近和小于硅带隙。这些实验表明,阳极氧化反应途径是由内部载流子重分布(即自掺杂空穴)控制的。我们引入了一个“电场预算”框架来量化电子转移和偏置时间对电化学动力学的累积效应。我们报告了半导体中电场诱导的电子转移──特别是由界面能量势垒决定的时间积分和累积势垒──在没有适当的外部激发的情况下能够发生化学或电化学反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Materials Au
ACS Materials Au 材料科学-
CiteScore
5.00
自引率
0.00%
发文量
0
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
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