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Efficient electrochemical hydrogen evolution reaction and solar activity via bi-functional GO/ Co_3O_4-TiO_2 nano hybrid structure

机译:通过双功能GO / CO_3O_4-TiO_2纳米混合结构的高效电化学氢进化反应和太阳能活性

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Highly proficient electro and solar catalyst of mixed metal oxides Co3O4-TiO2 modified with graphene oxide (GO) have been synthesized by simple and cost-effective way using sol-gel methodology. This catalyst demonstrated versatile bi-functional features towards the hydrogen evolution reaction (HER) in catalytic water splitting along with solar photo catalytic activity in the degradation of Methyl Orange (MO). XRD profile confirmed that composite presented an anatase and cubic phase for TiO2 and Co3O4, respectively, with the GO network. The morphological structures confirm flaky texture of Co3O4 with small irregular spheres of TiO2 nanoparticles randomly dispersed on the broken sheets of GO. GO and clusters of Co2+/Co3+ in different regions of host TiO2 are accountable for decreasing band gap in the composite samples. Co-O-Ti and Co-Ti-C linkages in the composite materials are confirmed by Raman and FTIR studies. In electro catalytic HER in alkaline medium GO/Co3O4-TiO2 catalyst illustrated low onset potential similar to 343 mV vs. RHE, high current density similar to 43 mA cm(-2) corresponding small Tafel slope similar to 97 mV/dec and small Rct as compared to other catalysts. For HER in GO/Co3O4-TiO2, Co2+ sites are more catalytically active than Co3+ sites along with Ti4+ and GO provides the more active surface area by reducing the agglomeration between the mixed metal oxides. GO/Co3O4-TiO2 shows the highest photo catalytic performance over MO as compared to binary and ternary composites. Pining of metal oxides with reactive oxygen functional moieties of GO considerably improve the photo catalytic degradation activity and helpful in the separation of charge carriers for HER. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:使用溶胶 - 凝胶方法通过简单且经济高效的方式合成了用石墨烯(GO)改性的混合金属氧化物CO3O4-TiO2的高易熟的电催化剂。该催化剂在催化水分解中朝向氢进化反应(她)以及在甲基橙(Mo)的降解中的太阳能光催化活性以及太阳能光催化活性的通用双功能特征。 XRD型谱分别确认复合材料分别用GO网络呈现TiO2和CO3O4的锐钛矿和立方相。形态学结构确认Co3O4的片状纹理,TiO2纳米粒子的小不规则球体随机分散在损坏的去底板上。在宿主TiO2的不同区域中的GO和CO2 + / CO3 +的簇是对复合样品中的带隙的降低负责。复合材料中的CO-O-TI和CO-TI-C键通过拉曼和FTIR研究证实。在电催化催化剂中,碱性介质GO / CO3O4-TiO2催化剂所示的低发病潜力类似于343mV与rhe,高电流密度类似于43 mA cm(-2)相应的小TAFEL斜率,类似于97 MV / DEC和小RCT与其他催化剂相比。对于在Go / CO3O4-TiO 2中,CO 2 +位点比CO3 +位点与TI4 +更催化有效,通过降低混合金属氧化物之间的聚集来提供更活跃的表面积。与二元和三元复合材料相比,Go / Co3O4-TiO2显示出在Mo上的最高照片催化性能。具有反应性氧官能的金属氧化物的潜水部分可显着改善光催化降解活性,并有助于为她的电荷载体分离。 (c)2020氢能源出版物LLC。 elsevier有限公司出版。保留所有权利。

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