吸附
甲醛
咪唑酯
材料科学
化学工程
超细纤维
氧化物
锌
比表面积
纳米材料
异质结
金属有机骨架
活性炭
纳米技术
碳纤维
选择性吸附
沸石咪唑盐骨架
纤维
纳米复合材料
纳米颗粒
作者
Zhiwen Jia,Yuqiong He,Jiayi Liu,Xinyi Yu,Shusheng Pang,Linkun Xie,Wanxi Peng,Guanben Du,Kaimeng Xu
出处
期刊:Small
[Wiley]
日期:2026-02-18
卷期号:: e13955-e13955
标识
DOI:10.1002/smll.202513955
摘要
An innovative strategy of heterointerface-driven formaldehyde capture was developed by dual metal organic framework (MOF) nanoarchitectures in-situ grown on bamboo microfibers (BMFs). The hierarchical BMF/MOF adsorbents were fabricated using steam-exploded BMFs as cores, followed by the sequential growth of indium-based MOF (MIL-68) on zeolitic imidazolate framework-8 (ZIF-8). This triggered a clear transition in adsorption behavior from physical adsorption to a chemisorption-dominated process, achieving ultra-efficient adsorption capacity of 268.15 mg g-1 with 19.72 times enhancements over commercial activated carbon (AC). The enhanced mechanism was the synergistic effects on the increase of the specific surface area, the formation of hierarchical pores, the introduction of the pyrrolic N and pyridinic N groups, and the formation of zinc oxide-indium oxide (ZnO-In2O3) heterojunction that changed the surface polarity and local electron density of the samples. The strategic hybridization of In2O3 and ZnO facilitates their electrostatic interactions with formaldehyde molecules, resulting in a significant increase in adsorption energies, varying from -7.91 kcal mol-1 (pristine BMF) to -24.28, -18.94, and -34.76 kcal mol-1 for single ZIF-8, MIL-68, and dual MOF-functionalized systems, respectively, representing remarkable enhancements of 206.95%, 139.43%, and 339.44%. The resultant BMF@MIL-68@ZIF-8-800 adsorbent shows the excellent formaldehyde remediation ability in real indoor scenario.
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