One-pot synthesis of N-doped petroleum coke-based microporous carbon for high-performance CO2 adsorption and supercapacitors.

Waste resource utilization of petroleum coke is crucial for achieving global carbon emission reduction. Herein, a series of N-doped microporous carbons were fabricated from petroleum coke using a one-pot synthesis method. The as-prepared samples had a large specific surface area (up to 2512 m2/g), a moderate-high N content (up to 4.82 at.%), and high population (55%) of ultra-micropores (<0.7 nm). Regulating the N content and ultra-microporosity led to efficient CO2 adsorption and separation. At ambient pressure, the optimal N-doped petroleum coke-based microporous carbon exhibited the highest CO2 uptake of 4.25 mmol/g at 25°C and 6.57 mmol/g at 0°C. These values are comparable or even better than those of numerous previously reported adsorbents prepared by multistep synthesis, primarily due to the existence of ultra-micropores. The sample exhibited excellent CO2/N2 selectivity at 25°C owing to the abundant basic pyridinic and pyrrolic N species; and showed superior CO2 adsorption-desorption cycling performance, which was maintained at 97% after 10 cycles at 25°C. Moreover, petroleum coke-based microporous carbon, with a considerably high specific surface area and hierarchical pore structure, exhibited excellent electrochemical performance over the N-doped sample, maintaining a favorable specific capacitance of 233.25 F/g at 0.5 A/g in 6 mol/L KOH aqueous electrolyte. This study provides insight into the influence of N-doping on the porous properties of petroleum coke-based carbon. Furthermore, the as-prepared carbons were found to be promising adsorbents for CO2 adsorption, CO2/N2 separation and electrochemical application.

High-Performance C60 Coupled Ferroelectric Enhanced MoS2 Nonvolatile Memory.

Nonvolatile memory (NVM) devices based on two-dimensional (2D) materials have recently attracted widespread attention due to their high-density integration potential and the ability to be applied in computing-in-memory systems in the post-Moore era. Considering the high current on/off ratio, programmable threshold voltage, nonvolatile multilevel memory state, and extended logic functions, plenty of breakthroughs related to ferroelectric field-effect transistors (FeFETs), one of the most important NVM devices, have been made in the past decade. Among them, FETs coupled with organic ferroelectric films such as P(VDF-TrFE) displayed properties of remarkable robustness, easy preparation, and low cost. However, the dipoles of the P(VDF-TrFE) film cannot be flipped smoothly at low voltage, impeding the further application of organic FeFET. In this paper, we proposed a high-performance FeFET based on monolayer MoS2 coupled with C60 doped ferroelectric copolymer P(VDF-TrFE). The inserted C60 molecules enhanced the alignment of the dipoles effectively at low voltage, allowing the modified device to demonstrate a large memory window (∼16 V), high current on/off ratio (>106), long retention time (>10 000 s), and remarkable endurance under the reduced operating voltage. In addition, the in situ logic application can be realized by constructing facile device interconnection without building complex complementary semiconductor circuits. Our results are expected to pave the way for future low-consumption computing-in-memory applications based on high-quality 2D FeFETs.

Precise preparation of biomass-based porous carbon with pore structure-dependent VOCs adsorption/desorption performance by bacterial pretreatment and its forming process.

Pore distribution characteristic is one of the most crucial factors for porous adsorption materials, and the variety of volatile organic compounds (VOCs) approaches about how to simply and accurately tailor practical porous carbons for VOCs adsorption has gradually attracted attention. Here, precursors with different lignocellulose mass ratios have been used to produce porous carbon for model experiments to investigate the influence of the precursor lignocellulose contents on the pore structure and distribution characteristics of porous carbon, and the applicability of these mechanisms to real biomass materials has been further verified through bacteria-targeted bagasse decomposition: the microvolumes of ultra-micropores have decreased with decrease in cellulose contents, while mesopores have followed the reverse trend. The dynamic toluene adsorption/desorption performances of the obtained samples have been tested. The BACs-36 exhibits high toluene adsorption performance in low concentration with 635 mg/g while the BACs-48 shows excellent reusability in 10 times cycles. Based on this the balance between the adsorptive and regenerative capacities has been observed which indicates that carbon materials with abundant micropores and narrow mesopores have much better adsorption performance than porous carbon with a hierarchical pore structure, while the latter show better regeneration abilities than the former, which resulting in less desorption as a counter-acting force at the pore wall. Furthermore, the porous carbon has been shaped by one-step co-pyrolysis method using phenolic resin, which can not only maintain the hardness but also can avoid pore plugging phenomenon.

Preparing hierarchical porous carbon with well-developed microporosity using alkali metal-catalyzed hydrothermal carbonization for VOCs adsorption.

Biomass-derived porous carbonaceous materials are efficient adsorbents for VOCs, but their traditional preparation method, pyrolysis combined with activation, suffers from high energy consumption, equipment corrosion, and low pore-making efficiency, which hinders their large-scale practical application. A novel method of alkali metal-catalyzed hydrothermal carbonization coupling with chemical activation for the preparation of microporous carbon is presented. Porous carbon with well-developed microporosity deriving from corn husk were prepared through the hydrothermal carbonization using potassium persulfate (K2S2O8) as a catalyst and programmed heating activation process. And the products were applied to removal of typical oxygen-containing VOCs, ethyl acetate. The addition of K2S2O8 in hydrothermal carbonization accelerated the biomass hydrolysis, decomposed the biopolymer, and formed functional hydrochars. Potassium salts introduced into the hydrochars, which acted as an activator in this programmed heating activation process, formed a great deal of micropores. The specific surface area of micropores increased by 81%, and the specific surface area of micropores less than 1 nm increased by 180%. The introduction of K2S2O8 in preparation improved the adsorption performance of CH-based porous carbons 16.46% and 60.00% respectively at different preparation temperatures (600 °C and 800 °C). Basing on these results, the improvement of micropores less than 1 nm is directly related to the adsorption performance. This indicates that pores (<1 nm) respond well to the adsorption of ethyl acetate.

Key factors and primary modification methods of activated carbon and their application in adsorption of carbon-based gases: A review.

To achieve carbon neutrality, it is necessary to control carbon-based gas emissions to the atmosphere. Among the various carbon-based gas removal technologies reported to date, adsorption is considered one of the most promising because of its economic efficiency, reusability, and low energy consumption. Activated carbon is widely used to treat different types of carbon-based gases owing to its large specific surface area, abundant functional groups, and strong adsorption capacity. This paper reviews the recent research progress into activated carbon as an adsorbent for carbon-based gases. The key factors (i.e., specific surface area, pore structure, and surface functional groups) affecting the adsorption of carbon-based gases by activated carbon were analyzed. The main methods employed to modify activated carbon (i.e., surface oxidation, surface reduction, loading materials, and plasma modification methods) to improve its adsorption capacity are also discussed herein, along with the targeted applications of such material in the adsorption of different types of carbon-based gases (such as aldehydes, ketones, aromatic hydrocarbons, halogenated hydrocarbons, and carbon-based greenhouse gases). Finally, the future development directions and challenges of activated carbon are discussed. Our work will be expected to benefit the development of activated carbon exhibiting selective adsorption properties, and reduce the production costs of adsorbents.

Preparation of porous carbon based on partially degraded raw biomass by Trichoderma viride to optimize its toluene adsorption performance.

Volatile organic compounds (VOCs), which are usually organic compounds with boiling point in the range of 50 to 260°C, pose a serious threat to human health and ecological environment. In order to find an adsorbent with excellent adsorption effect on VOCs, activated carbon was prepared from corn bran partially degraded by Trichoderma viride, and the adsorption performance of the optimized porous carbon materials on toluene was studied. Physical and chemical properties (such as specific surface area, pore size distribution, and surface functional groups) of the activated carbon were characterized by scanning electron microscope (SEM), N2 adsorption/desorption experiences, Fourier-transform infrared (FTIR), and Raman and X-ray diffraction (XRD). The results showed that the specific surface area of corn bran reached 1896 m2/g and the total pore volume was 1.04 cm3/g after 15 days of microbial pretreatment. Dynamic simulation of adsorption experiment found that the saturated adsorption capacity of the pretreated carbon material was 237 mg/g at 100 ppm toluene concentration, which was 1.58 times of that of corn bran without microbial pretreatment. Generally, the improvement of adsorption performance may be mainly attributed to the increase of specific surface area, pore volume and the decrease of surface acidic groups.

Alternative block polyurethanes based on poly(3-hydroxybutyrate-co-4-hydroxybutyrate) and poly(ethylene glycol).

A series of amphiphilic alternative block polyurethane copolymers based on poly(3-hydroxybutyrate-co-4-hydroxybutyrate) (P3/4HB) and poly(ethylene glycol) (PEG) were synthesized by a coupling reaction between P3/4HB-diol and PEG-diisocyanate, with different 3HB, 4HB, PEG compositions and segment lengths. Stannous octanoate was used as catalyst. The chemical structure, alternative block arrangement, molecular weight and distribution were systematically characterized by FTIR, (1)H NMR, GPC and composition analysis. The thermal property was studied by DSC and TGA. Platelet adhesion study revealed that the alternative block polyurethanes possess excellent hemocompatibility. CCK-8 assay illuminated that the non-toxic block polyurethanes maintain rat aortic smooth muscle cells (RaSMCs) good viability. The in-vitro degradation of the copolymers in PBS buffer solution and in lipase buffer medium was investigated. Results showed that the copolymer films exhibit different degradation patterns in different media from surface erosion to diffusion bulk collapsing. The synthetic methodology for the alternative block polyurethanes provides a way to control the exact structure of the biomaterials and tailor the properties to subtle requirements.