首页|多酸辅助一步合成双金属掺杂的多孔g-C3N4及染料和Cr(Ⅵ)去除研究

多酸辅助一步合成双金属掺杂的多孔g-C3N4及染料和Cr(Ⅵ)去除研究

扫码查看
石墨相氮化碳(g-C3N4)由于其具有理想的微观结构和化学功能,在环境处理应用中的潜力引起了人们的广泛兴趣。本研究以多金属氧酸盐(NH4)4[Co(Ⅱ)Mo6O24H6](Co-Mo6)为前驱体,通过一种简单的一步热聚合法制备了 一系列Co和Mo共掺杂的多孔石墨相氮化碳(Co/Mo-CN)。CoMo6不仅起到氧化刻蚀作用制造多孔结构,还作为双金属掺杂源。与原始石墨相氮化碳(P-CN)相比,具有比表面积大,暴露活性位点丰富,光吸收能力强,带隙窄,光生载流子分离速率快及更负的导带电位等优点。这些优点使Co/Mo-CN对多种阳离子染料的吸附能力和可见光下光催化还原Cr(Ⅵ)能力显著提高,为优化具有良好性能的石墨相氮化碳基材料开辟了一条新的途径。
Polyoxometalate-assisted one-step synthesis of bimetal co-doped porous g-C3N4 for dyes and Cr(Ⅵ) removal
Graphitic carbon nitride(g-C3N4,denoted as CN)has gained significant attention for its poten-tial applications in treating environmental pollutants due to its unique microstructure and chemical proper-ties.In this study,porous CN co-doped with Co and Mo(Co/Mo-CN)was successfully synthesized using a convenient thermal polymerization method involving polyoxometalate precursor of(NH4)4[Co(Ⅱ)Mo6O24H6](CoMo6).The single-source precursor of CoMo6 was not only as a pore forming agent by oxi-dation etching,but also as a bimetallic doping source.Compared with pristine CN(P-CN),Co/Mo-CN possessed more advantages,such as high specific surface area,plentiful exposed active sites,extending the light absorption capability,rapid separation of photogenerated charge carriers,narrowed bandgap and more negative conduction band potential.As expected,the Co/Mo-CN exhibited a significant enhancement of adsorption ability for cationic dyes and photoreduction Cr(Ⅵ)under visible light irradiation compared to P-CN.This research opened a new pathway designing multifunctional CN-based materials.

graphitic carbon nitridepolyoxometalateporous nanostructureadsorptionphotocatalysis

毛蕊馨、王亚、刘刚、田苗苗、张雁南

展开 >

吉林工程技术师范学院化学与工业生物工程交叉学科研究院,吉林长春 130052

吉林工程技术师范学院生物与食品工程学院,吉林长春 130052

新型分子功能材料吉林省校企联合技术创新实验室,吉林长春 130052

石墨相氮化碳 多金属氧酸盐 多孔纳米结构 吸附 光催化

Science and Technology Development Project of Jilin ProvinceDoctoral Research Initiation Fund Project of Jilin Engineering

YDZJ202301ZYTS313BSKJ201918

2024

分子科学学报
中国化学会

分子科学学报

CSTPCD
影响因子:0.434
ISSN:1000-9035
年,卷(期):2024.40(3)