Isocyanate-treated graphite oxides （iGOs） were well-dispersed into the polystyrene （PS） thin films and formed a novel network structure. With control in fabrication, an iGOs-web layer was horizontally embedded nea...Isocyanate-treated graphite oxides （iGOs） were well-dispersed into the polystyrene （PS） thin films and formed a novel network structure. With control in fabrication, an iGOs-web layer was horizontally embedded near the surface of the films and thus formed a composite slightly doped by iGOs. This work demonstrated that the iGOs network can remarkably depress the dewetting process in the polymer matrix of the composite, while dewetting often leads to rupture of polymer films and is considered as a major practical limit in using polymeric materials above their glass transition temperatures （Tg）. Via annealing the 50-120 nm thick composite and associated neat PS films at temperatures ranging from 35℃ to 70 ℃ above Tg, surface morphology evolution of the films was monitored by atomic force microscopy （AFM）. The iGOs-doped PS exhibited excellent thermal stability, i.e., the number of dewetting holes was greatly reduced and the long-term hole growth was fairly restricted. In contrast, the neat PS film showed serious surface fluctuation and a final rupture induced by ordinary dewetting. The method developed in this work may pave a road to reinforce thin polymer films and enhance their thermal stability, in order to meet requirements by technological advances.展开更多
基金the start-up fund of Y.G.from both University of Michigan-Shanghai Jiao Tong University Joint InstituteSchool of Materials Science and Engineering at SJTU+4 种基金the National Science Foundation of China for financial support through the General Program(No.2157408)the foundation of Shanghai Sailing Plan(No,16YF1406100)the National Youth 1000 Talent Program of Chinathe Shanghai 1000 Talent Planthe Scientific Research Foundation for the Returned Overseas Chinese Scholars,State Education Ministry of China
文摘Isocyanate-treated graphite oxides （iGOs） were well-dispersed into the polystyrene （PS） thin films and formed a novel network structure. With control in fabrication, an iGOs-web layer was horizontally embedded near the surface of the films and thus formed a composite slightly doped by iGOs. This work demonstrated that the iGOs network can remarkably depress the dewetting process in the polymer matrix of the composite, while dewetting often leads to rupture of polymer films and is considered as a major practical limit in using polymeric materials above their glass transition temperatures （Tg）. Via annealing the 50-120 nm thick composite and associated neat PS films at temperatures ranging from 35℃ to 70 ℃ above Tg, surface morphology evolution of the films was monitored by atomic force microscopy （AFM）. The iGOs-doped PS exhibited excellent thermal stability, i.e., the number of dewetting holes was greatly reduced and the long-term hole growth was fairly restricted. In contrast, the neat PS film showed serious surface fluctuation and a final rupture induced by ordinary dewetting. The method developed in this work may pave a road to reinforce thin polymer films and enhance their thermal stability, in order to meet requirements by technological advances.
