催化作用
材料科学
锐钛矿
化学工程
甲醇
金红石
纳米颗粒
碳纳米管
碳纤维
纳米技术
光催化
复合材料
化学
复合数
有机化学
工程类
作者
Jialong Li,Lei Zhao,Xifei Li,Sue Hao,Zhenbo Wang
标识
DOI:10.1002/asia.201900264
摘要
A synchronous carbon-coating and interfacial-functionalizing approach is proposed for the fabrication of Mo-doped Mox Ti1-x O2-δ nanotubes (C@IF-MTNTs) under mild hydrothermal reaction with subsequent annealing as advanced catalyst supports for PtRu nanoparticles (NPs) towards methanol electrooxidation. The carbonation of glucose and Mo-doping takes place simultaneously at the interface of pristine anatase TiO2 nanotubes (TNTs), generating a unique concentric multilayered one-dimensional (1D) structure with crystalline an anatase/rutile mixed-phase TiO2 core and Mo-functionalized interface and subsequently a carbon shell. The obtained PtRu/C@IF-MTNTs catalyst exhibits an over 2 times higher mass activity with comparable durability than that of the unmodified PtRu/C@TNTs catalyst and over 1.7 times higher mass activity with over 20 % higher stability than that of PtRu/C catalyst. Such superior catalytic performance towards methanol electrooxidation is ascribed to the Mo-functionalized interface, concentric multilayered 1D architecture, and anatase/rutile mixed-phase core, which facilitates the charge transport through 1D structural support and electronic interaction between C@IF-MTNTs and ultrafine PtRu NPs. This work reveals the critical application of a 1D interfacial functionalized architecture for advanced energy storage and conversion.
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