在石墨烯溶液中以乙醇溶解聚合物残留物 - - 网关场效应晶体管
Juan Pedro Merino1, Sergi Brosel-Oliu2, Gemma Rius2
1Center for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Paseo de Miramon 194, Donostia-San Sebastián 20014, Spain.
概括
光电阻的残留物阻碍了石墨烯电子. 乙醇溶剂有效地去除这些污染物,提高了石墨烯溶液门场效应晶体管 (gSGFET) 的性能,并使设备制造更绿色,更精确.
科学领域:
- 材料科学 材料科学 材料科学
- 纳米技术 纳米技术
- 表面化学 表面化学
背景情况:
- 微制造中的光电阻残留物阻碍了基于石墨烯的电子设备的性能.
- 污染物导致不良的兴奋剂,减少载体的移动性,以及像石墨烯溶液门场效应晶体管 (gSGFET) 这样的设备中的信号-噪声降解.
- 目前的微型制造技术在很大程度上依赖于聚合物,在残留物管理方面几乎没有直接的替代方案.
研究的目的:
- 评估设计后处理方法,以从石墨烯设备中去除光电阻残留物.
- 研究残留聚合物对石墨烯表面特性和gSGFET功能的影响.
- 确定一种有效,可持续和安全的残留物清除方法.
主要方法:
- 利用X射线光电子光谱 (XPS),原子力显微镜 (AFM) 和拉曼光谱进行全面分析.
- 进行了石墨烯溶液门式场效应晶体管 (gSGFET) 的电气表征.
- 比较了四氨酸 (THF) 和乙醇作为模式后清洁溶剂的有效性.
主要成果:
- 乙醇处理被证明是去除残留物最有效,最环保,最安全的方法.
- 乙醇清洗显著提高了gSGFET的性能,由一个移动的电荷中性点和减少设备变异性表明.
- 表面分析证实了聚合物污染物的去除,改善了石墨烯表面的性能.
结论:
- 用乙醇进行模式后清洁是一种可行的策略,可以提高石墨烯设备制造的可重复性和精度.
- 以乙醇为基础的清洁方法与绿色化学原则保持一致,最大限度地减少对环境的影响.
- 这种方法有助于在敏感的石墨烯应用中取得进展,例如传感和电气记录.
相关概念视频
Solvating Effects
7.4K
An understanding of the solvating effect helps rationalize the relation between solvation and acidity of the compound. In addition, this also explains the relative stability of conjugate bases for compounds with different pKa values. This lesson details, in-depth, the principle of solvating effects. The strength of an acid and the stability of its corresponding conjugate base are determined using pKa values. This observed relationship is a consequence of solvation, which is the interaction...
7.4K
Physical Properties of Ethers
7.0K
Overview
An ether molecule has a net dipole moment due to the polarity of C–O bonds. Subsequently, boiling points of ethers are lower than those of alcohols of comparable molecular weight and slightly higher than those of hydrocarbons of comparable molecular weight (Table 1).
Ethers can act as hydrogen bond acceptors, making them more water-soluble than hydrocarbons, but since ethers cannot act as hydrogen bond donors, they are much less soluble in water than alcohols. Ethers are considered...
An ether molecule has a net dipole moment due to the polarity of C–O bonds. Subsequently, boiling points of ethers are lower than those of alcohols of comparable molecular weight and slightly higher than those of hydrocarbons of comparable molecular weight (Table 1).
Ethers can act as hydrogen bond acceptors, making them more water-soluble than hydrocarbons, but since ethers cannot act as hydrogen bond donors, they are much less soluble in water than alcohols. Ethers are considered...
7.0K
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
10.3K
Overview
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
10.3K


