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化学活化共价三嗪框架具有增强的纹理特性,用于高容量气体存储。

Chemically Activated Covalent Triazine Frameworks with Enhanced Textural Properties for High Capacity Gas Storage.

机构信息

Graduate School of Energy, Environment, Water and Sustainability (EEWS), Korea Advanced Institute of Science and Technology (KAIST) , Daejeon 34141, Republic of Korea.

Department of Chemistry, University of Fribourg , Fribourg 1700, Switzerland.

出版信息

ACS Appl Mater Interfaces. 2017 Sep 13;9(36):30679-30685. doi: 10.1021/acsami.7b08930. Epub 2017 Aug 30.

Abstract

Chemical activation of porous/nonporous materials to achieve high surface area sorbents with enhanced textural properties is a very promising strategy. The chemical activation using KOH, however, could lead to broad distribution of pores originating from the simultaneous pore deepening and widening pathways. Accordingly, establishing correlation between the chemical/textural properties of starting porous/nonporous materials and various pore formation mechanisms is quite critical to realize superior porosity and gas uptake properties. Here, we show that the chemical and textural properties of starting porous organic polymers, that is, covalent triazine frameworks (CTF), have profound effect on the resulting porosity of the frameworks. The chemical activation of microporous CTF-1 using KOH at 700 °C enabled the preparation of chemically activated CTF-1, caCTF-1-700, which predominantly showed pore deepening, leading to an increased surface area of 2367 m g and significantly enhanced gas adsorption properties with CO uptake capacities up to 6.0 mmol g at 1 bar and 1.45 mmol g at 0.15 bar and 273 K along with a isosteric heats of adsorption (Q) of 30.6 kJ mol. In addition, a remarkable H uptake capacity of 2.46 and 1.66 wt % at 77 and 87 K, 1 bar along with the Q value of 10.95 kJ mol at zero coverage was also observed for the caCTF-1-700. Notably, the activation of mesoporous CTF-2 under the same conditions was accompanied by a decrease in its surface area and also in the conversion of mesopores into the micropores, thus leading to a pore deepening/narrowing rather than widening. We attributed this result to the presence of reactive weak spots, triazine moieties, for the chemical activation reaction within the CTF backbone. These results collectively suggest the critical role of chemical and pore characteristics of porous organic polymers in chemical activation to realize solid-sorbents for high capacity gas storage applications.

摘要

化学激活多孔/无孔材料以获得具有增强的结构特性的高表面积吸附剂是一种非常有前途的策略。然而,使用 KOH 的化学激活可能导致源于同时的孔加深和变宽途径的广泛分布的孔。因此,建立起始多孔/无孔材料的化学/结构特性与各种孔形成机制之间的相关性对于实现优异的多孔性和气体吸收性能至关重要。在这里,我们表明起始多孔有机聚合物,即共价三嗪框架(CTF)的化学和结构特性对框架的最终孔隙率有深远的影响。使用 KOH 在 700°C 下对微孔 CTF-1 的化学激活使制备了化学激活的 CTF-1,即 caCTF-1-700,其主要表现为孔加深,导致表面积增加至 2367 m²/g,并显著增强了气体吸附性能,在 1 bar 和 273 K 下,CO 的吸附量高达 6.0 mmol/g,在 0.15 bar 和 273 K 下,CO 的吸附量高达 1.45 mmol/g,吸附热(Q)为 30.6 kJ/mol。此外,在 77 和 87 K 下,在 1 bar 时,caCTF-1-700 的 H 吸附量分别为 2.46 和 1.66wt%,在零覆盖率时的 Q 值为 10.95 kJ/mol。值得注意的是,在相同条件下,介孔 CTF-2 的活化伴随着其表面积的降低,以及介孔转化为微孔,从而导致孔的加深/变窄而不是变宽。我们将这一结果归因于 CTF 骨架中存在用于化学激活反应的反应性弱点,即三嗪基团。这些结果共同表明了多孔有机聚合物的化学和孔特性在化学激活中实现高容量气体储存应用的固体吸附剂的关键作用。

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