Okoroanyanwu Uzodinma, Bhardwaj Ayush, Watkins James J
Department of Polymer Science & Engineering, University of Massachusetts at Amherst, 120 Governors Drive, Amherst, Massachusetts 01002, United States.
ACS Appl Mater Interfaces. 2023 Mar 15;15(10):13495-13507. doi: 10.1021/acsami.2c19894. Epub 2023 Feb 28.
We report a method for fast, efficient, and scalable preparation of high-quality, large area, few-layer graphene films on arbitrary substrates via high-intensity pulsed xenon flash lamp photothermal pyrolysis of thin precursor films at ambient conditions in millisecond time frames. The precursors comprised poly(2,2-bis(3,4-dihydro-3-phenyl-1,3-benzoxazine)), and cyclized polyacrylonitrile and possess significant absorption cross section within the bandwidth of the emission spectrum of a xenon flash lamp. By localizing light absorption to the precursor films, the process enabled the preparation of few-layer graphene films on any substrate, including thermally sensitive substrates without the need for any catalytic substrate as in chemical vapor deposition-based approaches or conductive electrodes as in electrochemical method-based approaches. The extent of conversion of the precursor films to graphene was strongly dependent on pulse energy and the local temperature achieved due to photothermal effect, which were controlled via pulse power modulation; it also depended on structural properties of the precursor and to a lesser extent on the substrate. The cPAN showed a higher efficiency for conversion to graphene, as confirmed by Raman spectra (/ ∼ 0.3), and sheet resistance of 0.1 Ω cm. To demonstrate the utility of the process, graphene film electrodes prepared photothermally on carbon fiber current collector were used for the fabrication of micro-supercapacitors with a very high areal supercapacitance of 3.5 mF/cm. Subsequent deposition of manganese oxide onto the fabricated electrodes significantly increased the energy storage capability of the supercapacitor, yielding a device with exceptionally high capacitance of 80 F/g at 1 mA current, good rate capability, and long cycle life.
我们报道了一种在环境条件下,通过高强度脉冲氙闪光灯对薄前驱体膜进行光热裂解,在任意衬底上快速、高效且可扩展地制备高质量、大面积、少层石墨烯薄膜的方法,整个过程在毫秒时间尺度内完成。前驱体包括聚(2,2 - 双(3,4 - 二氢 - 3 - 苯基 - 1,3 - 苯并恶嗪))和环化聚丙烯腈,它们在氙闪光灯发射光谱的带宽内具有显著的吸收截面。通过将光吸收定位在前驱体膜上,该方法能够在任何衬底上制备少层石墨烯薄膜,包括热敏衬底,无需像基于化学气相沉积的方法那样使用任何催化衬底,也无需像基于电化学方法的途径那样使用导电电极。前驱体膜向石墨烯的转化程度强烈依赖于脉冲能量以及由于光热效应所达到的局部温度,这通过脉冲功率调制来控制;它还取决于前驱体的结构性质,并且在较小程度上依赖于衬底。拉曼光谱(/ ∼ 0.3)和0.1 Ω cm的薄层电阻证实,环化聚丙烯腈显示出更高的转化为石墨烯的效率。为了证明该方法的实用性,在碳纤维集流体上光热制备的石墨烯薄膜电极被用于制造具有3.5 mF/cm非常高的面积比电容的微型超级电容器。随后在制造的电极上沉积氧化锰显著提高了超级电容器储能能力,得到了一种在1 mA电流下具有80 F/g的超高电容、良好的倍率性能和长循环寿命的器件。