A systematic study of atmospheric pressure chemical vapor deposition growth of large-area monolayer graphene.

Lixin Liu, Hailong Zhou, Rui Cheng, Yu Chen, Yung-Chen Lin, Yongquan Qu, Jingwei Bai, Ivan A Ivanov, Gang Liu, Yu Huang, Xiangfeng Duan
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引用次数: 73

Abstract

Graphene has attracted considerable interest as a potential material for future electronics. Although mechanical peel is known to produce high quality graphene flakes, practical applications require continuous graphene layers over a large area. The catalyst-assisted chemical vapor deposition (CVD) is a promising synthetic method to deliver wafer-sized graphene. Here we present a systematic study on the nucleation and growth of crystallized graphene domains in an atmospheric pressure chemical vapor deposition (APCVD) process. Parametric studies show that the mean size of the graphene domains increases with increasing growth temperature and CH4 partial pressure, while the density of domains decreases with increasing growth temperature and is independent of the CH4 partial pressure. Our studies show that nucleation of graphene domains on copper substrate is highly dependent on the initial annealing temperature. A two-step synthetic process with higher initial annealing temperature but lower growth temperature is developed to reduce domain density and achieve high quality full-surface coverage of monolayer graphene films. Electrical transport measurements demonstrate that the resulting graphene exhibits a high carrier mobility of up to 3000 cm2 V-1 s-1 at room temperature.

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常压化学气相沉积生长大面积单层石墨烯的系统研究。
石墨烯作为一种潜在的未来电子材料引起了人们的极大兴趣。虽然已知机械剥离可以生产高质量的石墨烯薄片,但实际应用需要大面积连续的石墨烯层。催化辅助化学气相沉积(CVD)是一种很有前途的制备晶圆级石墨烯的合成方法。本文系统地研究了常压化学气相沉积(APCVD)工艺中结晶石墨烯畴的成核和生长。参数化研究表明,石墨烯畴的平均尺寸随生长温度和CH4分压的升高而增大,而畴的密度随生长温度的升高而减小,且与CH4分压无关。我们的研究表明,石墨烯畴在铜衬底上的成核高度依赖于初始退火温度。提出了一种初始退火温度较高、生长温度较低的两步合成工艺,以降低畴密度,获得高质量的单层石墨烯薄膜的全表面覆盖。电输运测量表明,所得石墨烯在室温下表现出高达3000 cm2 V-1 s-1的高载流子迁移率。
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来源期刊
Journal of Materials Chemistry
Journal of Materials Chemistry 工程技术-材料科学:综合
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1.5 months
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Improved anti-proliferative effect of doxorubicin-containing polymer nanoparticles upon surface modification with cationic groups. Anisotropic nanocrystal arrays organized on protein lattices formed by recombinant clathrin fragments. The effect of mineral coating morphology on mesenchymal stem cell attachment and expansion. Location-tuned relaxivity in Gd-doped mesoporous silica nanoparticles. Photoreactive elastin-like proteins for use as versatile bioactive materials and surface coatings.
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