Reduced graphene oxide as photocatalyst for CO2 reduction reaction(Conference Presentation)

Yu-Chung Chang
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Abstract

Photocatalytic conversion of carbon dioxide (CO2) to hydrocarbons such as methanol makes possible simultaneous solar energy harvesting and CO2 reduction. Our previous work is using graphene oxide (GO) as a promising photocatalyst for photocatalytic conversion of CO2 to methanol[1].When using graphene oxide as photocatalyst, the photocatalytic efficiency is 4-flod higher than TiO2 powder. GO has a lot of defects on the surface and those defects make sp2 carbon structure become sp3 carbon structure. The carbon structure change cause the GO has large energy gap about 2.7 eV to 3.2 eV. In order to remove the defect and reduce the energy gap of GO, Zhao et al. try to annealing GO powder in the nitrogen atmosphere at 900oC, the GO structure can be reduced to near graphene structure[2]. Zhu et al. do some low temperature annealing, it can control the structure and energy bandgap of GO by control annealing temperature. If the annealing temperature increase the bandgap of GO will be reduce[3]. So, we can using this annealing process to reduce the bandgap of the GO. In the varying temperature thermal reduction process, as the temperature increases from 130oC to 170oC, the functional groups of the graphene oxide will be reduced and band gap of graphene oxide will be narrowed at same time. The characteristic of thermal reduced graphene oxide were analyzed by SEM, XRD and Raman measurements. The band position was determined by UV/Vis. The reduction of functional groups correlates to red shift in light absorption and eventual quenching in the PL signal of RGOs. Combining hydrophobicity, light harvesting and PL quench, we get the highest yield of RGO150 (0.31 μmole g-1 -cat hr-1) is 1.7-fold higher than that of GO (0.18μmole g-1 -cat hr-1). This work investigates a modified method for using a thermal reduction process to reduce the energy gap of graphene oxide.
还原氧化石墨烯作为CO2还原反应的光催化剂(会议报告)
光催化将二氧化碳(CO2)转化为碳氢化合物,如甲醇,使同时收集太阳能和减少二氧化碳成为可能。我们之前的工作是使用氧化石墨烯(GO)作为光催化将CO2转化为甲醇[1]的有前途的光催化剂。当使用氧化石墨烯作为光催化剂时,光催化效率比TiO2粉末高4倍。氧化石墨烯表面有很多缺陷,这些缺陷使得sp2碳结构变成了sp3碳结构。碳结构的改变使氧化石墨烯具有较大的能隙,约为2.7 ~ 3.2 eV。为了去除缺陷,减小氧化石墨烯的能隙,Zhao等人尝试将氧化石墨烯粉末在900℃的氮气气氛中退火,可以将氧化石墨烯结构还原为接近石墨烯结构的[2]。Zhu等人做了一些低温退火,可以通过控制退火温度来控制氧化石墨烯的结构和能隙。随着退火温度的升高,氧化石墨烯的带隙减小。因此,我们可以利用这种退火工艺来减小氧化石墨烯的带隙。在变温热还原过程中,随着温度从130℃升高到170℃,氧化石墨烯的官能团会减少,同时氧化石墨烯的带隙也会缩小。采用扫描电镜(SEM)、x射线衍射(XRD)和拉曼光谱(Raman)对热还原氧化石墨烯进行了表征。紫外/可见光谱法测定了光谱带的位置。官能团的减少与rgo光吸收的红移和PL信号的最终猝灭有关。结合疏水性、光收获和PL猝灭,得到了RGO150的最高产率(0.31 μmol g-1 -cat hr-1),是氧化石墨烯(0.18μmol g-1 -cat hr-1)的1.7倍。本文研究了一种改进的方法,使用热还原过程来减少氧化石墨烯的能隙。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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