• 专利标题:   Preparation of side gating graphene field-effect transistor structure involves placing copper foil in reaction chamber, vacuumizing reaction chamber, performing thermal annealing on copper foil, and growing graphene.
  • 专利号:   CN103000535-A, CN103000535-B
  • 发明人:   WANG D, HAN D, ZHANG J, HAO Y, CHAI Z, NING J, YAN Y
  • 专利权人:   UNIV XIDIAN
  • 国际专利分类:   C23C016/44, H01L021/336
  • 专利详细信息:   CN103000535-A 27 Mar 2013 H01L-021/336 201362 Pages: 9 Chinese
  • 申请详细信息:   CN103000535-A CN10593954 31 Dec 2012
  • 优先权号:   CN10593954

▎ 摘  要

NOVELTY - Preparation of side gating graphene field-effect transistor structure involves placing copper foil in a reaction chamber, vacuumizing the reaction chamber at 90-130 degrees C, and performing thermal annealing on the copper foil for 2-60 minutes, growing the graphene by chemical vapor deposition, transferring the graphene to high-dielectric constant substrate, utilizing a lithography machine to expose source drain and side gating positions, and etching graphene at the side gating positions using an oxygen plasma etching machine with etching power of 100-1000W for 5-70 seconds. USE - Preparation of side gating graphene field-effect transistor structure (claimed). ADVANTAGE - The method efficiently and economically forms side gating graphene field-effect transistor structure. The modulation capability of side gating on a graphene conducting channel is improved. DETAILED DESCRIPTION - Preparation of side gating graphene field-effect transistor structure involves placing copper foil in a reaction chamber, vacuumizing the reaction chamber at 90-130 degrees C, and performing thermal annealing on the copper foil for 2-60 minutes, growing the graphene by chemical vapor deposition, transferring the graphene to high-dielectric constant substrate, utilizing a lithography machine to expose source drain and side gating positions, utilizing an oxygen plasma etching machine to etch the graphene at the side gating positions with etching power of 100-1000W for 5-70 seconds, cooling to room temperature, evaporating metal on sample by using an E-beam device, enabling the sample such that the to-be-placed metal is evaporated in acetone to perform ultrasonography, maintaining the vacuum degree of 2.1-6 Torr, then rinsing the sample in absolute ethyl alcohol, washing sample using deionized water, and finally drying sample using pure nitrogen.