National Engineering Research Center for Colloidal Materials and School of Chemistry and Chemical Engineering , Shandong University , 250100 Jinan , China.
ACS Appl Mater Interfaces. 2019 Feb 27;11(8):7927-7935. doi: 10.1021/acsami.8b19445. Epub 2019 Feb 7.
Self-detoxifying materials capable of both capture and destruction of chemical warfare agents (CWAs) are highly desirable for efficient personal protection and safe handling of contaminated materials. Developing new strategies to improve CWA removal efficiency of these materials is highly relevant to CWA purification technology. Herein, we present novel photothermally enhanced catalytic detoxification of CWA simulants and its application in self-detoxifying gas filters. The material design features a well-defined core-shell nanostructure (CSN) consisting of an inner photothermal material and an outer microporous catalyst. As a demonstration, the CSN was obtained by growing a Zr-based metal-organic framework (MOF), UiO-66-NH, onto bioinspired dopamine-melanin (Dpa) nanoparticles via heterogeneous nucleation induced by metal chelation. The resultant Dpa@UiO-66-NH CSN has increased the turnover frequency (TOF) of a nerve agent simulant, 4-nitrophenyl phosphate (DMNP), by 2.9- and 1.7-fold in the presence of NIR laser and simulated solar light, respectively. Further incorporation of Dpa@UiO-66-NH CSNs into polymer fibers by electrospinning has led to an even greater photothermal enhancement effect (5.8- and 3.2-fold TOF increase), achieving a faster DMNP degradation rate than the corresponding pure MOF powder for the first time and the shortest half-life of DMNP (1.8 min) among reported MOF-based self-detoxifying fabrics. The significant photothermal enhancement in the detoxification ability of Dpa@UiO-66-NH fabrics is attributed to the instantaneous heat transfer from the photothermal core to the catalytic shell and effective heat retention enabled by the surrounding polymer matrix. The Dpa@UiO-66-NH fabrics can be easily prepared on a large scale and demonstrate efficient protection against DMNP aerosols as stand-alone gas filters. This strategy of photothermally enhanced catalytic detoxification can be feasibly extended to other catalytic detoxification systems and holds promise for next-generation gas masks.
具有同时捕获和破坏化学战剂(CWA)能力的自解毒材料对于有效个人防护和安全处理污染材料非常理想。开发提高这些材料 CWA 去除效率的新策略与 CWA 净化技术密切相关。在此,我们提出了一种新的光热增强催化解毒 CWA 模拟物的方法,并将其应用于自解毒气体过滤器。该材料设计的特点是具有明确定义的核壳纳米结构(CSN),由内光热材料和外微孔催化剂组成。作为一个演示,通过金属螯合诱导的异质成核,将基于锆的金属有机骨架(MOF)UiO-66-NH 生长在生物启发的多巴胺-黑色素(Dpa)纳米粒子上,得到了 CSN。所得的 Dpa@UiO-66-NH CSN 在存在 NIR 激光和模拟太阳光的情况下,神经毒剂模拟物 4-硝基苯膦酸二甲酯(DMNP)的周转频率(TOF)分别提高了 2.9 倍和 1.7 倍。通过静电纺丝将 Dpa@UiO-66-NH CSN 进一步掺入聚合物纤维中,导致光热增强效应更大(TOF 增加 5.8 倍和 3.2 倍),首次实现了比相应的纯 MOF 粉末更快的 DMNP 降解速率,并且在报道的基于 MOF 的自解毒织物中 DMNP 的半衰期最短(1.8 分钟)。Dpa@UiO-66-NH 织物解毒能力的显著光热增强归因于光热核向催化壳的瞬时热传递和周围聚合物基质实现的有效热保持。Dpa@UiO-66-NH 织物可以很容易地大规模制备,并作为独立的气体过滤器有效地防止 DMNP 气溶胶。这种光热增强催化解毒策略可以方便地扩展到其他催化解毒系统,为下一代防毒面具提供了希望。