4.8 Article

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

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 9, Issue 36, Pages 30679-30685

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.7b08930

Keywords

pore narrowing ionothermal synthesis; H-2 storage; porous organic polymers; CO2 capture

Funding

  1. National Research Foundation of Korea (NRF) Grant - Korea government (MEST) [2017R1A2B4004634]
  2. BK21 PLUS
  3. National Research Foundation of Korea [2017R1A2B4004634] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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 degrees 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(2) g(-1) and significantly enhanced gas adsorption properties with CO2 uptake capacities up to 6.0 mmol g(-1) at 1 bar and 1.45 mmol g(-1) at 0.15 bar and 273 K along with a isosteric heats of adsorption (Q(st)) of 30.6 kJ mol(-1). In addition, a remarkable H-2 uptake capacity of 2.46 and 1.66 wt % at 77 and 87 K, 1 bar along with the Q(st) value of 10.95 kJ mol-1 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.

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