Browsing by Author "Feng, Xu"

Now showing 1 - 5 of 5
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    Biochar Surface Oxygenation by Ozonization for Super High Cation Exchange Capacity
    Kharel, Gyanendra; Sacko, Oumar; Feng, Xu; Morris, John R.; Phillips, Claire L.; Trippe, Kristin; Kumar, Sandeep; Lee, James W. (2019-10-07)
    Biochar cation exchange capacity (CEC) is a key property central to better retention of soil nutrients and reduction of fertilizer runoff. This paper reports a breakthrough process to improve biochar CEC value by a factor of nearly 10 through biochar surface oxygenation by ozonization. The CEC value of the untreated biochar was measured to be anywhere between 14 and 17 cmol/kg. A 90 min dry ozonization treatment resulted in an increased biochar CEC value of 109-152 cmol/kg. Simultaneously, the biochar ozonization process resulted in a reduction of biochar pH from 9.82 to as low as 3.07, indicating the formation of oxygen-functional groups including carboxylic acids on biochar surfaces. Using the technique of X-ray photoelectron spectroscopy (XPS), the formation of oxygen-functional groups including carboxylic acids on biochar surfaces have been observed at a nanometer molecular scale following the ozonization treatment. The molar O/C ratio (0.31:1) on ozonized biochar surface as analyzed by XPS was indeed significantly higher than that (0.16:1) of the control biochar surface. The molar O/C ratio from the elemental analysis data also showed an increase from the nonozonized sample (0.077:1) to the dry-ozonized sample (0.193:1). Fourier-transform infrared (FTIR) spectroscopy analysis also showed an increase in the content of oxygen-functional groups in the form of carbonyl groups on biochar surfaces upon ozonization, which can also produce certain amount of oxygenated biochar molecular fragments that may be solubilized by liquid water, potentially leading to greater effects upon application of biochar in soil.
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    Biogenic formation of amorphous carbon by anaerobic methanotrophs and select methanogens
    Allen, Kylie D.; Wegener, Gunter; Sublett, D. Matthew, Jr.; Bodnar, Robert J.; Feng, Xu; Wendt, Jenny; White, Robert H. (AAAS, 2021-10-27)
    Elemental carbon exists in different structural forms including graphite, diamond, fullerenes, and amorphous carbon. In nature, these materials are produced through abiotic chemical processes under high temperature and pressure but are considered generally inaccessible to biochemical synthesis or breakdown. Here, we identified and characterized elemental carbon isolated from consortia of anaerobic methanotrophic archaea (ANME) and sulfate-reducing bacteria (SRB), which together carry out the anaerobic oxidation of methane (AOM). Two different AOM consortia, ANME-1a/HotSeep-1 and ANME-2a/c/Seep-SRB, produce a black material with similar characteristics to disordered graphite and amorphous carbon. Stable isotope probing studies revealed that the carbon is microbially generated during AOM. In addition, we found that select methanogens also produce amorphous carbon with similar characteristics to the carbon from AOM consortia. Biogenic amorphous carbon may serve as a conductive element to facilitate electron transfer, or redox active functional groups associated with the carbon could act as electron donors and acceptors.
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    Interaction of Na, O₂, CO₂ and water on MnO(100): Modeling a complex mixed oxide system for thermochemical water splitting
    Feng, Xu (Virginia Tech, 2015-10-14)
    A catalytic route to hydrogen production via thermochemical water splitting is highly desirable because it directly converts thermal energy into stored chemical energy in the form of hydrogen and oxygen. Recently, the Davis group at Caltech reported an innovative low-temperature (max 850°C) catalytic cycle for thermochemical water splitting based on sodium and manganese oxides (Xu, Bhawe and Davis, PNAS, 2012). The key steps are thought to be hydrogen evolution from a Na₂CO₃/MnO mixture, and oxygen evolution by thermal reduction of solids formed by Na⁺ extraction from NaMnO₂. Our work is aimed at understanding the fundamental chemical processes involved in the catalytic cycle, especially the hydrogen evolution from water. In this project, efforts are made to understand the interactions between the key components (Na, O₂, CO₂, and water) in the hydrogen evolution steps on a well-defined MnO(100) single crystal surface, utilizing x-ray photoelectron spectroscopy (XPS), low energy electron diffraction (LEED) and temperature programmed desorption (TPD). While some of the behavior of the catalytic system is observed with the model system developed in this work, hydrogen is only produced from water in the presence of metallic sodium, in contrast to the proposal of Xu et al. that water splitting occurs from the reaction of water with a mixture of Na₂CO₃ and MnO. These differences are discussed in light of the different operating conditions for the catalytic system and the surface science model developed in this work.
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    Screen-Printed Soft-Nitrided Carbon Electrodes for Detection of Hydrogen Peroxide
    Ogbu, Chidiebere I.; Feng, Xu; Dada, Samson N.; Bishop, Gregory W. (MDPI, 2019-08-29)
    Nitrogen-doped carbon materials have garnered much interest due to their electrocatalytic activity towards important reactions such as the reduction of hydrogen peroxide. N-doped carbon materials are typically prepared and deposited on solid conductive supports, which can sometimes involve time-consuming, complex, and/or costly procedures. Here, nitrogen-doped screen-printed carbon electrodes (N-SPCEs) were fabricated directly from a lab-formulated ink composed of graphite that was modified with surface nitrogen groups by a simple soft nitriding technique. N-SPCEs prepared from inexpensive starting materials (graphite powder and urea) demonstrated good electrocatalytic activity towards hydrogen peroxide reduction. Amperometric detection of H2O2 using N-SPCEs with an applied potential of −0.4 V (vs. Ag/AgCl) exhibited good reproducibility and stability as well as a reasonable limit of detection (2.5 µM) and wide linear range (0.020 to 5.3 mM).
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    Ultrahigh Durability Perovskite Solar Cells
    Wu, Congcong; Wang, Kai; Feng, Xu; Jiang, Yuanyuan; Yang, Dong; Hou, Yuchen; Yan, Yongke; Sanghadasa, Mohan; Priya, Shashank (American Chemical Society, 2019-01-29)
    Unprecedented conversion efficiency has been demonstrated for perovskite solar cells (PSCs), however, their stability and reliability continue to be challenge. Here, an effective and practical method is demonstrated to overcome the device stability issues in PSCs. A CF4 plasma treatment method is developed that results in the formation of a robust C–Fx layer covering the PSC device, thereby, imparting protection during the operation of solar cell. PSCs exposed to fluorination process showed excellent stability against water, light, and oxygen, displaying relatively no noticeable degradation after being dipped into water for considerable time period. The fluorination process did not have any impact on the morphology and electrical property of the top Spiro-OMeTAD layer, resulting in a conversion efficiency of 18.7%, which is identical to that of the pristine PSC. Under the continuous Xe lamp (AM 1.5G, 1 sun) illumination in ambient air for 100 h, the fluorinated PSCs demonstrated 70% of initial conversion efficiency, which is 4000% higher than that of the pristine PSC devices. We believe this breakthrough will have significant impact on the transition of PSCs into real world applications.