Ke Feng, Zhang Lingkong, Chen Yabin, Yin Ketao, Wang Chenxu, Tzeng Yan-Kai, Lin Yu, Dong Hongliang, Liu Zhenxian, Tse John S, Mao Wendy L, Wu Junqiao, Chen Bin
Center for High Pressure Science and Technology Advanced Research, Shanghai 201203, China.
Department of Geological Sciences, Stanford University, Stanford, California 94305, United States.
Nano Lett. 2020 Aug 12;20(8):5916-5921. doi: 10.1021/acs.nanolett.0c01872. Epub 2020 Jul 1.
Atomically thin diamond, also called diamane, is a two-dimensional carbon allotrope and has attracted considerable scientific interest because of its potential physical properties. However, the successful synthesis of a pristine diamane has up until now not been achieved. We demonstrate the realization of a pristine diamane through diamondization of mechanically exfoliated few-layer graphene via compression. Resistance, optical absorption, and X-ray diffraction measurements reveal that hexagonal diamane (h-diamane) with a bandgap of 2.8 ± 0.3 eV forms by compressing trilayer and thicker graphene to above 20 GPa at room temperature and can be preserved upon decompression to ∼1.0 GPa. Theoretical calculations indicate that a (-2110)-oriented h-diamane is energetically stable and has a lower enthalpy than its few-layer graphene precursor above the transition pressure. Compared to gapless graphene, semiconducting h-diamane offers exciting possibilities for carbon-based electronic devices.
原子级薄的金刚石,也称为二亚甲基,是一种二维碳同素异形体,因其潜在的物理性质而引起了科学界的广泛关注。然而,迄今为止尚未成功合成出纯净的二亚甲基。我们通过对机械剥离的少层石墨烯进行压缩使其金刚石化,证明了纯净二亚甲基的实现。电阻、光吸收和X射线衍射测量表明,通过在室温下将三层及更厚的石墨烯压缩至20 GPa以上,形成了带隙为2.8±0.3 eV的六方二亚甲基(h-二亚甲基),并且在减压至约1.0 GPa时仍可保留。理论计算表明,在转变压力以上,(-2110)取向的h-二亚甲基在能量上是稳定的,并且比其少层石墨烯前驱体具有更低的焓。与无带隙的石墨烯相比,半导体h-二亚甲基为碳基电子器件提供了令人兴奋的可能性。