2020
DOI: 10.3390/polym12051193
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High-Molecular-Weight PLA-b-PEO-b-PLA Triblock Copolymer Templated Large Mesoporous Carbons for Supercapacitors and CO2 Capture

Abstract: High-molecular-weight PLA440-b-PEO454-b-PLA440 (LEL) triblock copolymer was synthesized through simple ring-opening polymerization (ROP) by using the commercial homopolymer HO-PEO454-OH as the macro-initiator. The material acted as a single template to prepare the large mesoporous carbons by using resol-type phenolic resin as a carbon source. Self-assembled structures of phenolic/LEL blends mediated by hydrogen bonding interaction were determined by FTIR and SAXS analyses. Through thermal curing and carbonizat… Show more

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Cited by 23 publications
(19 citation statements)
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“…The preparation of porous organic polymers (POPs) has become a hot topic in the academic and industry fields due to their interesting features, such as high physicochemical stability, porous character, low density, facile preparation, low regeneration energy, and good thermal and chemical stabilities [ 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 ]. Porous organic polymers have been applied in different applications such as light harvesting, chemical sensors, catalysis, iodine uptake, H 2 production from water, water treatment, optoelectronic devices, carbon dioxide reduction, nanofiltration, enantioseparation, energy storage, gas separation, and adsorption [ 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 ]. The synthesis of POPs was successfully achieved using various synthetic methods, including Friedel–Crafts arylation, Schiff base reactions, Suzuki reactions, Yamamoto reactions, Heck reactions, and Sonogashira reactions [ 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 40 , 41 ].…”
Section: Introductionmentioning
confidence: 99%
“…The preparation of porous organic polymers (POPs) has become a hot topic in the academic and industry fields due to their interesting features, such as high physicochemical stability, porous character, low density, facile preparation, low regeneration energy, and good thermal and chemical stabilities [ 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 ]. Porous organic polymers have been applied in different applications such as light harvesting, chemical sensors, catalysis, iodine uptake, H 2 production from water, water treatment, optoelectronic devices, carbon dioxide reduction, nanofiltration, enantioseparation, energy storage, gas separation, and adsorption [ 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 ]. The synthesis of POPs was successfully achieved using various synthetic methods, including Friedel–Crafts arylation, Schiff base reactions, Suzuki reactions, Yamamoto reactions, Heck reactions, and Sonogashira reactions [ 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 40 , 41 ].…”
Section: Introductionmentioning
confidence: 99%
“…The BET surface area, total pore volume, and pore size diameter of the TPE-HPP were 922 m 2 g −1 , 0.86 cm 3 g −1 and 1.10 – 1.98 nm, respectively ( Figure 5 C ), while the DPT-HPP revealed a BET surface area, total pore volume and pore size diameter of 1230 m 2 g −1 , 1.03 cm 3 g −1 and 1.21–2.15 nm, respectively ( Figure 5 D ). Comparing with the reported HCPs, the specific surface area of our DPT-HPP (1230 m 2 g −1 ) was among the highest values of the other hypercrosslinked microporous polymers; for example, this includes the tetraphenylanthraquinone-based HCP (1980 m 2 g −1 ), binaphthol-based HCP (1015 m 2 g −1 ), and a porous organic polymer containing triazine and carbazole moieties (913 m 2 g −1 ) [ 20 , 58 , 59 , 60 ]. Furthermore, the SEM and TEM measurements were performed to confirm the porous properties of the TPE-HPP and DPT-HPP, as displayed in Figure 6 .…”
Section: Resultsmentioning
confidence: 91%
“…At 298 K and 1 bar pressure ( Figure 7 A ), the CO 2 adsorption capacity reached 1.65 and 1.85 mmol g −1 for the TPE-HPP and DPT-HPP, respectively, while the CO 2 capture was 1.91 and 2.06 mmol g −1 for the TPE-HPP and DPT-HPP, respectively, at 273 K ( Figure 7 B ). Both TPE-HPP and DPT-HPP exhibited higher values of CO 2 uptake than that of the tetraphenylanthraquinone-based HCPs such as An-CPOP-1 (1.30 mmol at 298 K and 1.40 mmol g −1 at 273 K) and An-CPOP-2 (1.40 mmol g −1 at 298 K and 1.52 mmol g −1 at 273 K) [ 20 ]. In addition, our materials showed higher CO 2 capture than silole-based HCPs (PDMTPAS, 1.02 mmol g −1 at 298 K), COF-102 (1.56 mmol g −1 at 273 K) and C2M1-Al (1.44 mmol g −1 at 273 K) [ 61 , 62 , 63 ].…”
Section: Resultsmentioning
confidence: 99%
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“…Most importantly, the signals at 1090 cm −1 for the Si–O–Si units and at 1265 cm −1 for the Si–CH 3 units were still present after thermal heating at 900 °C, suggesting that the DDSQ units remained dispersed within the carbon matrix in the carbon/DDSQ hybrids. Raman spectroscopy (HORIBA Jobin–yvon, T6400, Edison, NJ, USA) revealed the local graphitic structure of this carbon/DDSQ hybrid ( Figure 7 b), with two major carbonized structures identified by G- and D-bands representing sp 2 - and sp 3 -hybridized carbon atoms at 1592 and 1340 cm −1 , respectively [ 40 , 41 ]. The G- and D-bands correspond to first- and second-order Raman scattering, respectively; this G-band had undergone a major shift from the wavenumber of a typical G-band (ca.…”
Section: Resultsmentioning
confidence: 99%