Accurate Control of All-Polymer Hollow Multishelled Spheres by One-Step Reaction-Diffusion

被引:13
|
作者
Pan, Na [1 ]
Lin, Min [1 ]
Cui, Huilin [1 ]
Fan, Wenxin [1 ]
Liu, Chunzhao [1 ]
Chen, Fu [2 ]
Fan, Changjiang [3 ]
Xia, Yanzhi [1 ]
Sui, Kunyan [1 ]
机构
[1] Qingdao Univ, State Key Lab Biofibers & Ecotext, Shandong Collaborat Innovat Ctr Marine Biobased F, Coll Mat Sci & Engn, Qingdao 266071, Peoples R China
[2] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
[3] Qingdao Univ, Coll Med, Inst Translat Med, Qingdao 266071, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
CARBON NANOTUBES; MICROCAPSULES; MICROSPHERES; MEMBRANES; NANOPARTICLES;
D O I
10.1021/acs.chemmater.0c02437
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hollow multishelled structures (HoMSs) enable material intriguing properties and diverse applications. However, constructing all-polymer HoMSs (p-HoMSs) remains a great challenge. Here, we first develop a one-step self-template strategy to synthesize p-HoMS spheres through controlled reaction-diffusion of a polyelectrolyte pair. Besides instant reaction, the high concentration and moderate molecular weight of one polyelectrolyte as the self-template are required to fulfill the key conditions (i.e., high cross-linking density and high diffusion difference of the two reactants) for the p-HoMS sphere fabrication. In consequence, scalable p-HoMSs are rationally designed with structural and composition control, including shell number, core size, and morphology. More importantly, this p-HoMS could facilely template the synthesis of hierarchical macroscopic HoMS metal oxide with a shell number up to 12. This self-template strategy provides a simple, general, controllable, and large-scale way for the fabrication of HoMS materials with various compositions, complex structures, and diverse functions, signifying for a new methodology in material science.
引用
收藏
页码:8442 / 8449
页数:8
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