Study on Oxygen Evolution Reaction of Ir Nanodendrites Supported on Antimony Tin Oxide.

In this study, the iridium nanodendrites (Ir NDs) and antimony tin oxide (ATO)-supported Ir NDs (Ir ND/ATO) were prepared by a surfactant-mediated method to investigate the effect of ATO support and evaluate the electrocatalytic activity for the oxygen evolution reaction (OER). The nano-branched Ir ND structures were successfully prepared alone or supported on ATO. The Ir NDs exhibited major diffraction peaks of the fcc Ir metal, though the Ir NDs consisted of metallic Ir as well as Ir oxides. Among the Ir ND samples, Ir ND2 showed the highest mass-based OER catalytic activity (116 mA/mg at 1.8 V), while it suffered from high degradation in activity after a long-term test. On the other hand, Ir ND2/ATO had OER activity of 798 mA/mg, and this activity remained >99% after 100 cycles of LSV and the charge transfer resistance increased by less than 3 ohm. The enhanced durability of the OER mass activities of Ir ND2/ATO catalysts over Ir NDs and Ir black could be attributed to the small crystallite size of Ir and the increase in the ratio of Ir (III) to Ir (IV), improving the interactions between the Ir NDs and the ATO support.

Preparation of Zeolitic Imidazolate Framework-8-Based Nanofiber Composites for Carbon Dioxide Adsorption.

In this study, polyacrylonitrile (PAN)-based activated nanofiber composites, which were embedded inside zeolitic imidazolate framework-8 (ZIF-8) crystals or ZIF-8-derived carbons (ZDC-850), were fabricated using an electrospinning process, to serve as CO2 adsorbents. The adsorbents were characterized using various techniques. The degree of crystallinity of ZDC-850 totally changed compared to that of ZIF-8. For nanofiber composites, the timing of the ligand decomposition of ZIF-8 significantly affected the material properties. The Zn metals in the ZIF-8/PAN or ZDC-850/PAN could be embedded and protected by the PAN fibers from excess volatilization in the following treatments: ZIF-8 had significant pore volumes in the range of 0.9−1.3 nm, but ZDC-850 and ZIF-8/PAN exhibited a distinct peak at approximately 0.5 nm. The CO2 adsorption capacities at 25 °C and 1 atm followed the order: ZIF-8/PAN (4.20 mmol/g) > ZDC-850 (3.50 mmol/g) > ZDC-850/PAN (3.38 mmol/g) > PAN (2.91 mmol/g) > ZIF-8 (0.88 mmol/g). The slope in the log−linear plot of isosteric heat of adsorption was highly associated with CO2 adsorption performance. Under 1 atm at 25 °C, for Zn metal active sites inside the pores, the pores at approximately 0.5 nm and in C-N (amines) groups could promote CO2 adsorption. At low CO2 pressures, for a good CO2 adsorbent, the carbon content in the adsorbent should be higher than a threshold value. Under this condition, the percentage of ultra-micropore and micropore volumes, as well as the functional groups, such as the quaternary or protonated N (amines), N=C (imines or pyridine-type N), C-OH, and -COOH groups, should be considered as significant factors for CO2 adsorption.

The Application of Hollow Carbon Nanofibers Prepared by Electrospinning to Carbon Dioxide Capture.

Coaxial electrospinning has been considered a straightforward and convenient method for producing hollow nanofibers. Therefore, the objective of this study was to develop hollow activated carbon nanofibers (HACNFs) for CO2 capture in order to reduce emissions of CO2 to the atmosphere and mitigate global warming. Results showed that the sacrificing core could be decomposed at carbonization temperatures above 900 °C, allowing the formation of hollow nanofibers. The average outer diameters of HACNFs ranged from 550 to 750 nm, with a shell thickness of 75 nm. During the carbonization stage, the denitrogenation reactions were significant, while in the CO2 activation process, the release of carbon oxides became prominent. Therefore, the CO2 activation could increase the percentages of N=C and quaternary N groups. The major nitrogen functionalities on most samples were O=C-NH and quaternary N. However, =C and quaternary N groups were found to be crucial in determining the CO2 adsorption performance. CO2 adsorption on HACNFs occurred due to physical adsorption and was an exothermic reaction. The optimal CO2 adsorption performance was observed for HACNFs carbonized at 900 °C, where 3.03 mmol/g (1 atm) and 0.99 mmol/g (0.15 atm) were measured at 25 °C. The degradation of CO2 uptakes after 10 adsorption-desorption cyclic runs could be maintained within 8.9%.

Effect of Relative Humidity on Adsorption Breakthrough of CO2 on Activated Carbon Fibers.

Microporous activated carbon fibers (ACFs) were developed for CO2 capture based on potassium hydroxide (KOH) activation and tetraethylenepentamine (TEPA) amination. The material properties of the modified ACFs were characterized using several techniques. The adsorption breakthrough curves of CO2 were measured and the effect of relative humidity in the carrier gas was determined. The KOH activation at high temperature generated additional pore networks and the intercalation of metallic K into the carbon matrix, leading to the production of mesopore and micropore volumes and providing access to the active sites in the micropores. However, this treatment also resulted in the loss of nitrogen functionalities. The TEPA amination has successfully introduced nitrogen functionalities onto the fiber surface, but its long-chain structure blocked parts of the micropores and, thus, made the available surface area and pore volume limited. Introduction of the power of time into the Wheeler equation was required to fit the data well. The relative humidity within the studied range had almost no effects on the breakthrough curves. It was expected that the concentration of CO2 was high enough so that the impact on CO2 adsorption capacity lessened due to increased relative humidity.

Enhanced CO2 Adsorption on Activated Carbon Fibers Grafted with Nitrogen-Doped Carbon Nanotubes.

In this paper, multiscale composites formed by grafting N-doped carbon nanotubes (CNs) on the surface of polyamide (PAN)-based activated carbon fibers (ACFs) were investigated and their adsorption performance for CO2 was determined. The spaghetti-like and randomly oriented CNs were homogeneously grown onto ACFs. The pre-immersion of cobalt(II) ions for ACFs made the CNs grow above with a large pore size distribution, decreased the oxidation resistance, and exhibited different predominant N-functionalities after chemical vapor deposition processes. Specifically, the CNs grafted on ACFs with or without pre-immersion of cobalt(II) ions were characterized by the pyridine-like structures of six-member rings or pyrrolic/amine moieties, respectively. In addition, the loss of microporosity on the specific surface area and pore volume exceeded the gain from the generation of the defects from CNs. The adsorption capacity of CO2 decreased gradually with increasing temperature, implying that CO2 adsorption was exothermic. The adsorption capacities of CO2 at 25 °C and 1 atm were between 1.53 and 1.92 mmol/g and the Freundlich equation fit the adsorption data well. The isosteric enthalpy of adsorption, implying physical adsorption, indicated that the growth of CNTs on the ACFs benefit CO2 adsorption.

Characterization of Platinum Nanoparticles Deposited on Functionalized Graphene Sheets.

Due to its special electronic and ballistic transport properties, graphene has attracted much interest from researchers. In this study, platinum (Pt) nanoparticles were deposited on oxidized graphene sheets (cG). The graphene sheets were applied to overcome the corrosion problems of carbon black at operating conditions of proton exchange membrane fuel cells. To enhance the interfacial interactions between the graphene sheets and the Pt nanoparticles, the oxygen-containing functional groups were introduced onto the surface of graphene sheets. The results showed the Pt nanoparticles were uniformly dispersed on the surface of graphene sheets with a mean Pt particle size of 2.08 nm. The Pt nanoparticles deposited on graphene sheets exhibited better crystallinity and higher oxygen resistance. The metal Pt was the predominant Pt chemical state on Pt/cG (60.4%). The results from the cyclic voltammetry analysis showed the value of the electrochemical surface area (ECSA) was 88 m²/g (Pt/cG), much higher than that of Pt/C (46 m²/g). The long-term test illustrated the degradation in ECSA exhibited the order of Pt/C (33%) > Pt/cG (7%). The values of the utilization efficiency were calculated to be 64% for Pt/cG and 32% for Pt/C.

Characterization and application of Ti-containing mesoporous silica for dye removal with synergistic effect of coupled adsorption and photocatalytic oxidation.

Highly ordered mesoporous silica, Santa Barbara Amorphous-15 (SBA-15), and titanium-substituted mesoporous silica (TiSBA-15) materials were successfully synthesized, characterized, and evaluated. The textual and structural properties of the prepared materials with various titanium contents were characterized by inductively coupled plasma-mass spectrometer (ICP-MS), powder X-ray diffraction (XRD) patterns, nitrogen physisorption isotherms, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). A limited content of titanium could be effectively substituted into the framework of SBA-15 without provoking structure change. The adsorptive performance was examined by methylene blue (MB) adsorbed on prepared materials. The isotherm models were analyzed to describe the adsorption behavior of prepared materials. The adsorption isotherms were well-fitted with Langmuir and Freundlich models in the simulation of the adsorption behavior of dyes. The SBA-15 and TiSBA-15 materials were found to be effective adsorbents for MB from aqueous solutions. The photodegradation of MB and total organic carbon (TOC) analysis on solid composites were used to evaluate the catalytical performance of Ti-containing mesoporous silica. The synergistic effect of adsorptive and photocatalytical ability of prepared TiSBA-15 was identified. The regeneration and cyclic performance were also proved. These results revealed that TiSBA-15 could be one effective alternative material for dye removal.

Adsorption equilibrium of sulfur hexafluoride on multi-walled carbon nanotubes.

The adsorption of sulfur hexafluoride (SF(6)) on multi-walled carbon nanotubes (MWNTs) was investigated. The properties of MWNTs were characterized and the adsorption capacities of SF(6) on MWNTs at different concentrations and temperatures were collected. H(2)SO(4)/H(2)O(2) oxidation or KOH activation of MWNTs has effectively introduced the surface oxides and modified the microstructure without destruction of their graphitic crystalline structure. The MWNTs, especially the modified samples, are expected to be promising adsorbents for SF(6) removals from air. The saturated capacities of SF(6) with a concentration of 518 ppmv on the MWNTs ranged from 278 to 497 mg/g at 25 degrees C. The Toth equation has been reported to fit the adsorption data better than the Freundlich or Langmuir equation. The pi-pi dispersion interaction followed by the multi-layer adsorption and the electron donor-acceptor interaction were proposed to be the major adsorption mechanisms, depending on the adsorption temperature. The isosteric heat of adsorption, ranging from 51 to 124 kJ/mol with a loading of 30-300 mg/g, decreased with increasing SF(6) loading, reflecting the energetic heterogeneity of the MWNTs. These results suggest that the adsorption of SF(6) on MWNTs could be associated with binding to defect sites.