| 1. |
- Geng, Longlong, et al.
(författare)
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Valence-mixed CuOx-nanoparticles anchored biomass-based carbon nanofiber for boosting toxic nitroarenes reduction : Synthesis, kinetics, and mechanisms
- 2022
-
Ingår i: Journal of Environmental Chemical Engineering. - : Elsevier. - 2213-3437. ; 10:6
-
Tidskriftsartikel (refereegranskat)abstract
- The rational modulation of metal catalysts with tailorable valence and redox properties is a promising strategy for further improving their catalytic performance. Herein, an environment-friendly grafting and thermal strategy was adopted to immobilize copper oxides nanoparticles on carbon nanofiber (CuOx/CF). Benefiting from the defect-rich surface and valence-mixed composition of the CuOx species, the optimized sample CuOx/CF-3 exhibits superb activity for the catalytic reduction of toxic nitrophenols. The complete conversion took only 1 min and an outstanding rate constant (k) of 112.7 × 10-3 s-1 was achieved under mild conditions (25 °C and 1 atm). Kinetic and recycle experiments demonstrated that the whole catalytic process obeys a pseudo-order kinetic, and the catalyst could maintain high conversion even after 13 successive recycles. These results demonstrate that CuOx/CF-3 is an alternative catalyst to noble metals, providing superb catalytic efficiency and stability in the reduction of toxic nitrophenols, and it can be expanded to develop other noble-metal-free catalysts for various applications.
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| 2. |
- Zhang, Yunqiu, et al.
(författare)
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Nanomanganese cobaltate-decorated halloysite nanotubes for the complete degradation of ornidazole via peroxymonosulfate activation
- 2023
-
Ingår i: Journal of Colloid and Interface Science. - : Elsevier. - 0021-9797 .- 1095-7103. ; 630, s. 855-866
-
Tidskriftsartikel (refereegranskat)abstract
- Peroxymonosulfate (PMS) driven by halloysite nanotubes (HNTs) modified with nanomanganese cobaltate (MnCo2O4) generates reactive oxygen species (ROS) that offer high degradation efficiency and mineralization rates for many typical antibiotic pollutants, such as ornidazole (ONZ). The experimental results show that halloysite nanotubes (HNTs) modified with nanomanganese cobaltate (MnCo2O4@HNTs denoted as MCO@HNTs) can degrade ONZ completely over a wide pH range (6.08–11.00) with little influence of the pH value. MCO@HNTs + PMS exhibited higher catalytic activity and lower Co- and Mn-ion leaching rates. It also showed a strong anti-interference effect on natural lake water and anions. Additionally, PMS can be quickly activated and consumed in natural lakes to avoid secondary pollution. The roasting of MCO@HNTs showed good catalytic activity and stability after degrading ONZ. The combination of ion quenching and electron paramagnetic resonance (EPR) analysis illustrated that the MCO@HNTs + PMS system had a strong oxidation capacity, and the produced singlet oxygen (1O2) was the main ROS for ONZ degradation. The degradation pathway of ONZ via the MCO@HNTs + PMS system was proposed based on the types of intermediates determined via liquid chromatography-mass spectrometry (LC-MS). This comprehensive study shows the preparation of a simple, environmentally friendly, and cheap PMS activation catalyst that has practical application value in the treatment of antibiotic wastewater and provides a focus on actual water testing with residual amount of PMS.
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| 3. |
- Zhao, Xue, et al.
(författare)
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Two-dimensional BCN matrix inlaid with single-atom-Cu driven electrochemical nitrate reduction reaction to achieve sustainable industrial-grade production of ammonia
- 2021
-
Ingår i: APPLIED MATERIALS TODAY. - : Elsevier. - 2352-9407. ; 25
-
Tidskriftsartikel (refereegranskat)abstract
- Electrochemical methods have been proven to effectively eliminate nitrates in sewage and convert them into high value-added ammonia products. Here, after annealing treatment of metal boron cluster organic polymers formed by the combination of 1,10-phenanthroline, Cu2+ and closo-[B12H12](2)(-), a Cu single-atom doped BCN (B-doped CN) with a diamond-shaped nanosheet structure was obtained. In the electrochem-ical reduction reaction of nitrate, BCN-Cu exhibits excellent catalytic activity, specifically: 1) the ammonia yield rate reached as high as 498.85 mu g h(-1) cm(-2), 1047.14 mu g h(-1) cm(-2), 1900.07 mu g h(-1) cm(-2) and 3358.74 mu g h(-1) cm(-2) at -0.3 V, -0.4 V, -0.5 V and -0.6 V vs reversible hydrogen electrode, respectively, and Faradaic efficiency is 95.90%, 97.28%, 98.23% and 97.37%; 2) after repeated use of BCN-Cu 10 times or continuous operation for 16 h, the activity against electrochemical reduction reaction of nitrate anions is almost unchanged. The (NO3-)-N-15 isotopic labeling experiment proved that the detected NH3 comes from the reduction of NO3- on BCN-Cu. Control experiments show that the presence of Cu determines whether BCN-Cu has the possibility of catalyzing electrochemical reduction reactions of nitrate, and the presence of the B element enhances the catalytic activity of BCN-Cu. Density functional calculations indicate that in the water phase the process of reducing NO3- to NH3 on Cu-0 is an exothermic reaction, and that the adsorption process of NO3- on Cu-0 is the rate-determining step.
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| 4. |
- Huang, Ruihua, et al.
(författare)
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Star-shaped porous nitrogen-doped metal-organic framework carbon as an electrochemical platform for sensitive determination of Cd(II) in environmental and tobacco samples
- 2022
-
Ingår i: Analytica Chimica Acta. - : Elsevier. - 0003-2670 .- 1873-4324. ; 1228
-
Tidskriftsartikel (refereegranskat)abstract
- In this study, cetyltrimethylammonium bromide and zeolitic imidazolate framework-8 (ZIF-8) were first assembled via the chemical co-precipitation, and high-quality carbon-based metal-free nanomaterials were synthesized using a heat-treatment process. The internal and morphological characteristics of hexagonal Star ZIF-8 were investigated using scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The electrochemical sensor with a good response to Cd(II) was prepared via square-wave anodic stripping voltammetry (SWASV) with Star ZIF-8 nanomaterial-modified glassy carbon electrodes. The main parameters were adjusted to obtain the optimal stripping response and a wide linear range. Concurrently, under the calculation of SWASV, the sensitivity of Star ZIF-8-Nafion/GCE to Cd(II) was increased by five orders of magnitude (0.5–230 μg/L), and the determination level was even low to 0.48 μg/L. Based on the high anti-interference ability and stability of the sensor, the application potential of Star ZIF-8 carbon-based metal-free nanomaterials for the detection of trace Cd(II) in was confirmed.
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| 5. |
- Jia, Xiuxiu, et al.
(författare)
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Mesopore-rich badam-shell biochar for efficient adsorption of Cr(VI) from aqueous solution
- 2021
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Ingår i: Journal of Environmental Chemical Engineering. - : Elsevier. - 2213-3437. ; 9:4
-
Tidskriftsartikel (refereegranskat)abstract
- Cr(VI) is a common pollutant in wastewater and many previous studies using biochar-based materials as adsorbents for their well adsorption performance. However, the preparations of some biochars are complex, uneconomical, and with a poor reusability, which set limit on their practical application. Here, a mesoporous-rich biochar-based Cr(VI) adsorbent was easily prepared by pyrolyzing the badam-shell that in situ activated by concentrated phosphoric acid (H3PO4), with the aim of improving the removal effect of Cr(VI) in an aqueous solution. The partition coefficient (PC) was used to compare the performance of adsorbents more comprehensively, and the maximal PC value of the activated badam-shell biochar (ABSB) was 978.8 L g-1. In addition, its maximum adsorption capacity was 276.6 mg g-1. ABSB has a superior removal effect on the relatively low concentration of Cr(VI) (= 50 mg L-1), and residual Cr(VI) can meet the maximum emission standard (< 0.5 mg L-1) of industrial wastewater. The specific surface area of ABSB (1359.5 m2 g-1) was approximately four times that of pristine badam-shell biochar (BSB) (371.87 m2 g-1). The adsorption mechanisms involved were redox, complexation, electrostatic attraction and hydrogen bonding. The removal rate of Cr(VI) on ABSB remained at 81.6% after six cycles of adsorption-desorption. In a word, our study provides a simple, economic, and environmental method in fabricating the new adsorbent, which is highly promising and will not cause secondary pollution.
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| 6. |
- Peng, Yan, et al.
(författare)
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Cu Nanoparticle-Decorated Boron-Carbon-Nitrogen Nanosheets for Electrochemical Determination of Chloramphenicol
- 2022
-
Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 14:25, s. 28956-28964
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Tidskriftsartikel (refereegranskat)abstract
- In the present work, irregular Cu nanoparticle-decorated boron-carbon-nitrogen (Cu-BCN) nanosheets were successfully synthesized. A Cu-BCN dispersion was deposited on a bare glassy carbon electrode (GCE) to prepare an electrochemical sensor (Cu-BCN/GCE) for the detection of chloramphenicol (CAP) in the environment. Cu-BCN was characterized using high-resolution scanning transmission electron microscopy (HRSTEM), scanning electron microscopy (SEM), X-ray diffraction (XRD) analysis, and X-ray photoelectron spectroscopy (XPS). The performance of the Cu-BCN/GCE was studied using electrochemical impedance spectroscopy (EIS), and its advantages were proven by electrode comparison. Differential pulse voltammetry (DPV) was used to optimize the experimental conditions, including the amount of Cu-BCN deposited, enrichment potential, deposition time, and pH of the electrolyte. A linear relationship between the CAP concentration and current response was obtained under the optimized experimental conditions, with a wide linear range and a limit of detection (LOD) of 2.41 nmol/L. Cu-BCN/GCE exhibited high stability, reproducibility, and repeatability. In the presence of various organic and inorganic species, the influence of the Cu-BCN-based sensor on the current response of CAP was less than 5%. Notably, the prepared sensor exhibited excellent performance in real-water samples, with satisfactory recovery.
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| 7. |
- Zeng, Yanbo, et al.
(författare)
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A simple polypropylene fiber membrane embedded with clean La(OH)3 nanoparticles for highly efficient phosphate anions removal
- 2022
-
Ingår i: Journal of Environmental Chemical Engineering. - : Elsevier. - 2213-3437. ; 10:5
-
Tidskriftsartikel (refereegranskat)abstract
- Lanthanide materials are attracting increasing attention owing to their ability to strongly bind with phosphorus (P). In this paper, a novel method of producing clean lanthanum nano-aerosols by spark ablation is proposed, the particles are uniformly deposited on a cheap and readily available Polypropylene(PP) fiber membrane in a special gas environment, and combined with water (solvent) for hydrothermal synthesis of the new material, PP-La. Material characterization confirmed that the formation of La(OH)3 nanoparticles and ligand exchange plays an important role in the phosphorus adsorption process, extended X-ray absorption spectroscopy demonstrated that phosphate was bound to the lanthanum site. The adsorption capacity of PP-La for phosphate is 188.6 mg P/g La, and the cost index (capacity/synthesis cost) is 132.54 mg P/USD. In addition, unlike most sorbents, PP-La has the advantage of being easily separated from water. This synthesis method is green and simple, the lanthanum is not toxic, the Polypropylene fiber membrane is cheap and has better mechanical strength, and the application prospect is very broad. Our results provide a new strategy for the development of efficient adsorbents and the treatment of eutrophication by selective adsorption of phosphate in lakes, reservoirs, rivers, and other water bodies.
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| 8. |
- Zhang, Hua, et al.
(författare)
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3D Melamine Sponge-Derived Cobalt Nanoparticle-Embedded N-Doped Carbon Nanocages as Efficient Electrocatalysts for the Oxygen Reduction Reaction
- 2021
-
Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 6:31, s. 20130-20138
-
Tidskriftsartikel (refereegranskat)abstract
- The large-scale and controllable synthesis of novel N-doped three-dimensional (3D) carbon nanocage-decorated carbon skeleton sponges (Co-NCMS) is introduced. These Co-NCMS were highly active and durable non-noble metal catalysts for the oxygen reduction reaction (ORR). This hybrid electrocatalyst showed high ORR activity with a diffusion-limiting current of 5.237 mA·cm-2 in 0.1 M KOH solution through the highly efficient 4e- pathway, which was superior to that of the Pt/C catalyst (4.99 mA·cm-2), and the ORR Tafel slope is ca. 67.7 mV·dec-1 at a high potential region, close to that of Pt/C. Furthermore, Co-NCMS exhibited good ORR activity in acidic media with an onset potential comparable to that of the Pt/C catalyst. Most importantly, the prepared catalyst showed much higher stability and better methanol tolerance in both alkaline and acidic solutions. The power density obtained in a proton exchange membrane fuel cell was as high as 0.37 W·cm-2 at 0.19 V compared with 0.45 W·cm-2 at 0.56 V for the Pt/C catalyst. In Co-NCMS, the N-doped carbon nanocages facilitated the diffusion of the reactant, maximizing the exposure of active sites on the surface and protecting the active metallic core from oxidation. This made Co-NCMS one of the best non-noble metal catalysts and potentially offers an alternative approach for the efficient utilization of active transition metals in electrocatalyst applications.
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| 9. |
- Zhang, Hao, et al.
(författare)
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Recent advances in non-noble metal-based bifunctional electrocatalysts for overall seawater splitting
- 2022
-
Ingår i: Journal of Alloys and Compounds. - : Elsevier. - 0925-8388 .- 1873-4669. ; 922
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Forskningsöversikt (refereegranskat)abstract
- Since seawater is one of the most abundant resources on earth, seawater electrolysis is becoming increasingly attractive for clean energy/hydrogen production. Although significant progress has been made recently, it is still challenging to obtain bifunctional electrocatalysts with high catalytic activity and durability suitable for seawater electrolysis because of the scarcity of precious metals and inadequate state-of-the-art materials for the overall reaction. The development of high-performance bifunctional electrocatalysts is crucial to the commercialization of overall seawater electrolysis and in this review, the mechanism and challenges of seawater electrolysis are introduced. Optimization strategies for different types of non-noble-metal-based electrocatalysts including structural regulation, interface regulation, doping regulation, in situ assembly, alloying, and amorphization are summarized to elucidate the relationship among composition, structure, and properties. Finally, the challenge and prospective for future development of non-noble-metal-based bifunctional catalysts are discussed. This paper aims at providing guidance and insights into the rational design of highly efficient catalytic materials for practical seawater splitting.
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| 10. |
- Zhang, Ping, et al.
(författare)
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Deficiency of alkaline SMase enhances dextran sulfate sodium-induced colitis in mice with upregulation of autotaxin
- 2018
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Ingår i: Journal of Lipid Research. - 1539-7262. ; 59:10, s. 1841-1850
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Tidskriftsartikel (refereegranskat)abstract
- Intestinal alkaline SMase (Alk-SMase) cleaves phosphocholine from SM, platelet-activating factor (PAF), and lysophosphatidylcholine. We recently found that colitis-associated colon cancer was 4- to 5-fold enhanced in Alk-SMase KO mice. Here, we further studied the pathogenesis of colitis induced by dextran sulfate sodium (DSS) in WT and KO mice. Compared with WT mice, KO mice demonstrated greater body weight loss, more severe bloody diarrhea, broader inflammatory cell infiltration, and more serious epithelial injury. Higher levels of PAF and lower levels of interleukin (IL)10 were identified in KO mice 2 days after DSS treatment. A greater and progressive increase of lysophosphatidic acid (LPA) was identified. The change was associated with increased autotaxin expression in both small intestine and colon, which was identified by immunohistochemistry study, Western blot, and sandwich ELISA. The upregulation of autotaxin coincided with an early increase of PAF. IL6 and TNFα were increased in both WT and KO mice. At the later stage (day 8), significant decreases in IL6, IL10, and PAF were identified, and the decreases were greater in KO mice. In conclusion, deficiency of Alk-SMase enhances DSS-induced colitis by mechanisms related to increased autotaxin expression and LPA formation. The early increase of PAF might be a trigger for such reactions.
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| 11. |
- Zhang, Xin, et al.
(författare)
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Increasing Electrocatalytic Oxygen Evolution Efficiency through Cobalt-Induced Intrastructural Enhancement and Electronic Structure Modulation
- 2021
-
Ingår i: ChemSusChem. - : Wiley-VCH Verlagsgesellschaft. - 1864-5631 .- 1864-564X. ; 14:1, s. 467-478
-
Tidskriftsartikel (refereegranskat)abstract
- Electrolytic water splitting using surplus electricity represents one of the most cost-effective and promising strategies for hydrogen production. The high overpotential of the oxygen-evolution reaction (OER) caused by the multi-electron transfer process with a high chemical energy barrier, however, limits its competitiveness. Here, a highly active and stable OER electrocatalyst was designed through a cobalt-induced intrastructural enhancement strategy combined with suitable electronic structure modulation. A carved carbon nanobox was embedded with tri-metal phosphide from a uniform Ni-Co-Fe Prussian blue analogue (PBA) nanocube by sequential NH3 center dot H2O etching and thermal phosphorization. The sample exhibited an OER activity in an alkaline medium, reaching a current density of 10 mA cm(-2) at an overpotential of 182 mV and displayed a small Tafel slope of 47 mV dec(-1), superior to the most recently reported OER electrocatalysts. Moreover, it showed impressive electrocatalytic durability, increasing by approximately 2.7 % of operating voltage after 24 h of continuous testing. The excellent OER activity and stability are ascribed to a favorable transfer of mass and charge provided by the porous carbon shell, synergistic catalysis between the three-component metal phosphides originating from appropriate electronic structure modulation, more exposed catalytic sites on the hollow structure, and chainmail catalysis resulting from the carbon protective layer. It is foreseen that this successfully demonstrated design concept can be easily extended to other heterogeneous catalyst designs.
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| 12. |
- Zhao, Xue, et al.
(författare)
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Copper confined in vesicle-like BCN cavities promotes electrochemical reduction of nitrate to ammonia in water
- 2021
-
Ingår i: Journal of Materials Chemistry A. - : ROYAL SOC CHEMISTRY. - 2050-7488 .- 2050-7496. ; 9:41, s. 23675-23686
-
Tidskriftsartikel (refereegranskat)abstract
- Electrochemical methods to convert high-concentration nitrates present in sewage into high-value-added ammonia do not just alleviate the problem of environmental pollution but also provide less energy-intensive alternatives to the Haber-Bosch process. In this work, a metal-boron organic polymer precursor was annealed at high temperature to obtain copper nanoparticles encapsulated in a vesicle-like BCN matrix (BCN@Cu). In the electrochemical reduction of nitrate (E-NIRR), this species exhibited excellent catalytic activity. Specifically, the ammonia yields of BCN@Cu under applied potentials of -0.3 V, -0.4 V, -0.5 V, and -0.6 V versus the reversible hydrogen electrode were 271.1 mu mol h(-1) mg(cat.)(-1), 354.8 mu mol h(-1) mg(cat.)(-1), 435.6 mu mol h(-1) mg(cat.)(-1), and 576.2 mu mol h(-1) mg(cat.)(-1), respectively, and the corresponding Faraday efficiencies were 86.3%, 88.0%, 89.3%, and 88.9%. Isotope labeling experiments with (NO3-)-N-15 confirmed that the detected ammonia had originated from the electrochemical reduction of NO3- on the catalyst surface. Moreover, the E-NIRR activity of BCN@Cu remained high even after using it ten consecutive times or 20 h of continuous operation, suggesting the practicality of the industrial application of BCN@Cu. The presence of copper was key in determining BCN@Cus E-NIRR activity, while the presence of boron greatly improved its catalytic performance. Furthermore, density functional theory calculations indicated that BCN does not itself promote the reaction but rather assists the dispersion of Cu nanoparticles, thereby expanding the catalysts active surface area.
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| 13. |
- Zhao, Xue, et al.
(författare)
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Simultaneous anchoring of Ni nanoparticles and single-atom Ni on BCN matrix promotes efficient conversion of nitrate in water into high-value-added ammonia
- 2022
-
Ingår i: Chemical Engineering Journal. - : Elsevier. - 1385-8947 .- 1873-3212. ; 433:Part 2
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Tidskriftsartikel (refereegranskat)abstract
- Electrochemical synthesis of ammonia driven by clean energy is expected to realize the supply of ammonia for distributed production of industry and agriculture. Here, nickel nanoparticles and nickel in the form of single atoms were simultaneously anchored on the electrochemically active carrier BCN matrix through a structured domain strategy, which realized a high-efficiency, high-value-added, conversion of nitrate in sewage. Specifically, the electrochemical nitrate reduction reaction (NIRR) driven by BCN@Ni in alkaline media achieves an ammonia yield rate as high as 2320.2 μg h−1 cm−2 (at −0.5 V vs RHE), and Faraday efficiency as high as 91.15% (at −0.3 V vs RHE). Even in neutral and acidic media, the ammonia yield rates of NIRR driven by BCN@Ni are as high as 1904.2 μg h−1 cm−2 and 2057.4 μg h−1 cm−2, respectively (at −0.4 V vs RHE). The 15NO3- isotope labeling experiment verified that the recorded ammonia all came from the electrochemical reduction of NO3– on BCN@Ni. Density functional theory (DFT) calculations show that both nano-Ni and single-atom Ni in BCN@Ni have the ability to electrochemically convert NO3– into NH3, and that the addition of BCN can further promote the NIRR on Ni.
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| 14. |
- Bi, Zenghui, et al.
(författare)
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Highly dispersed La−O/N−C sites anchored in hierarchically porous nitrogen-doped carbon as bifunctional catalysts for high-performance rechargeable Zn−air batteries
- 2023
-
Ingår i: Energy Storage Materials. - : Elsevier. - 2405-8289 .- 2405-8297. ; 54, s. 313-322
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Tidskriftsartikel (refereegranskat)abstract
- Inexpensive, high-activity bifunctional catalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are imperative for the development of energy storage and conversion systems. A nitrogen-doped carbon material with a micro−meso−macroporous structure doped with La (LaPNC) containing La−O/N−C active sites is prepared using SiO2 particle templating of carbon and a metal node exchange strategy. The coordination environment of La sites stabilized by two oxygen and four nitrogen atoms (LaO2N4), is further verified by X-ray absorption spectroscopy. The ORR half-wave potential reaches 0.852 V, and the OER overpotential reaches 263 mV at 10 mA cm−2. The Zn−air battery, with LaPNC as the air cathode, has a maximum power density of 202 mW cm−2 and achieves stable charge−discharge for at least 100 h without a significant increase or decrease in the charge or discharge voltages, respectively. Density functional theory calculations suggest that LaO2N4 sites exhibit the lowest activation free energy and the most easily desorbed oxygen capacity. This study provides new insights into the design of efficient, durable bifunctional catalysts as alternatives to precious-metal-based catalysts.
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| 15. |
- Bi, Zenghui, et al.
(författare)
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Three dimensional star-like mesoporous nitrogen-doped carbon anchored with highly dispersed Fe and Ce dual-sites for efficient oxygen reduction reaction in Zn-air battery
- 2022
-
Ingår i: Colloid and Interface Science Communications. - : Elsevier. - 2215-0382. ; 49
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Tidskriftsartikel (refereegranskat)abstract
- Metal‑nitrogen‑carbon materials (M-N-C) have attracted much attention due to their low cost, high abundance, and efficient catalytic performance. Nevertheless, Fe-N-C materials are considered the most promising oxygen reduction reaction (ORR) catalysts for replacing noble metals. Ce is chemically active and has many metal valence states, and empty orbitals that can participate in coordination. On this basis, Fe, Ce-codoped catalyst was constructed in this study. The synergistic effect of the dual metal centers was verified, and a Fe, Ce-codoped nitrogen-doped carbon (FeCeNC) with six equal branch angles was proposed. The half-wave potential for the ORR catalyzed by FeCeNC is 0.855 V. As a rechargeable Zn-air battery cathode catalyst, FeCeNC exhibits excellent electrochemical performances, with an open-circuit voltage of 1.427 V, a maximum power density of 169.2 mW cm−2 and a stable cycling time of 80 h, demonstrating an excellent cycle performance.
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| 16. |
- Fan, Xiaoyu, et al.
(författare)
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Paper test strip for silver ions detection in drinking water samples based on combined fluorometric and colorimetric methods
- 2023
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Ingår i: Arabian Journal of Chemistry. - : Elsevier. - 1878-5352 .- 1878-5379. ; 16:2
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Tidskriftsartikel (refereegranskat)abstract
- In this study, a portable silver ion (Ag+) sensor was fabricated based on a dual signal output system using black phosphorus quantum dots (BPQDs) as probes. It is the first work for Ag+ detection using paper test strip based on BPQDs. The color change of BPQDs paper sensor for the determination of Ag+ was easily identified by naked eye. BPQDs were synthesized from bulk black phosphorus (BP) by mechanical exfoliation combined with a solvothermal method. BPQDs exhibited blue fluorescence with a quantum yield of 8.82 %. The fluorescence of BPQDs can be quenched by Ag+, and the absorbance of BPQDs is increased with increasing Ag+ concentration. The mechanism of the interaction between BPQDs and Ag+ involving fluorescence quenching and bonding was investigated by experimental and computational methods. The detection limit of Ag+ was 1.56 μg/mL and 0.19 μg/mL using fluorometry and colorimetry methods, respectively. A portable visual sensor based on paper test strip was constructed for Ag+ detection using the colorimetric approach. The strategy was employed to determine Ag+ successfully in drinking water samples. Therefore, the proposed portable Ag+ sensor can be potentially utilized for the lab-free analysis of drinking water and even dietary samples.
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| 17. |
- Flahou, Bram, et al.
(författare)
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Evidence for a primate origin of zoonotic Helicobacter suis colonizing domesticated pigs.
- 2018
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Ingår i: The ISME journal. - : Springer Science and Business Media LLC. - 1751-7370 .- 1751-7362. ; 12:1, s. 77-86
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Tidskriftsartikel (refereegranskat)abstract
- Helicobacter suis is the second most prevalent Helicobacter species in the stomach of humans suffering from gastric disease. This bacterium mainly inhabits the stomach of domesticated pigs, in which it causes gastric disease, but it appears to be absent in wild boars. Interestingly, it also colonizes the stomach of asymptomatic rhesus and cynomolgus monkeys. The origin of modern human-, pig- or non-human primate-associated H. suis strains in these respective host populations was hitherto unknown. Here we show that H. suis in pigs possibly originates from non-human primates. Our data suggest that a host jump from macaques to pigs happened between 100000 and 15000 years ago and that pig domestication has had a significant impact on the spread of H. suis in the pig population, from where this pathogen occasionally infects humans. Thus, in contrast to our expectations, H. suis appears to have evolved in its main host in a completely different way than its close relative Helicobacter pylori in humans.
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| 18. |
- Hao, Chenglin, et al.
(författare)
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Low-temperature molten-salt synthesis of Co3O4 nanoparticles grown on MXene can rapidly remove ornidazole via peroxymonosulfate activation
- 2023
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Ingår i: Environmental Pollution. - : Elsevier. - 0269-7491 .- 1873-6424. ; 334
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Tidskriftsartikel (refereegranskat)abstract
- We further developed previous work on MXene materials prepared using molten salt methodology. We substituted single, with mixed salts, and reduced the melting point from >724 °C to <360 °C. Cobalt (Co) compounds were simultaneously etched and doped while the MXene material was created using various techniques in which Co compounds occur as Co3O4. The synthesized Co3O4/MXene compound was used as a peroxymonosulfate (PMS) activator that would generate free radicals to degrade antibiotic ornidazole (ONZ). Under optimal conditions, almost 100% of ONZ (30 mg/L) was degraded within 10 min. The Co3O4/MXene + PMS system efficiently degraded ONZ in natural water bodies, and had a broad pH adaptation range (4–11), and strong anion anti-interference. We investigated how the four active substances were generated using radical quenching and electron paramagnetic resonance (EPR) spectroscopy. We identified 12 ONZ intermediates by liquid chromatography-mass spectrometry and propose a plausible degradative mechanism.
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| 19. |
- He, Yingnan, et al.
(författare)
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Separable amino-functionalized biochar/alginate beads for efficient removal of Cr(VI) from original electroplating wastewater at room temperature
- 2022
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Ingår i: Journal of Cleaner Production. - : Elsevier. - 0959-6526 .- 1879-1786. ; 373
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Tidskriftsartikel (refereegranskat)abstract
- An alginate gel bead composite adsorbent with polyethyleneimine (PEI) as a surface modifier and Eichhornia crassipes (EC) biochar, known as EC-alg/PEI-3, was added internally to the adsorb Cr(VI) from an aqueous environment. The functionalized gel beads were characterized using SEM, XPS, FTIR, and other techniques. The maximum adsorption capacities of EC-alg/PEI-3 were 714.3 mg g−1 at 10 °C and 769.2 mg g−1 at 25 °C. In the treatment of highly concentrated electroplating wastewater, EC-alg/PEI-3 can be dosed at 1.4 g L−1 to reduce the concentration of Cr(VI) to below 0.05 ppm. EC-alg/PEI-3 maintained a competitive adsorption capacity after six cycles. This spherical adsorbent material is easy to prepare, has a very high adsorption capacity, is environmentally friendly, and can be easily recycled. The EC-alg/PEI-3 gel beads are promising for the treatment of industrial wastewater.
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| 20. |
- He, Yingnan, et al.
(författare)
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Separatable MoS2 loaded biochar/CaCO3/Alginate gel beads for selective and efficient removal of Pb(II) from aqueous solution
- 2022
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Ingår i: Separation and Purification Technology. - : Elsevier. - 1383-5866 .- 1873-3794. ; 303
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Tidskriftsartikel (refereegranskat)abstract
- Centimeter-scale composite biochar-alginate gel beads (MoS2B/CaCO3/Alg) were designed for the adsorption of Pb(II) in water using MoS2 modified biochar as the filler, alginate as the matrix, and CaCO3 as the active additive component. The composite gel beads were characterized using scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR), X-ray diffraction (XRD), and other techniques. MoS2B/CaCO3/Alg showed excellent adsorption capacity over a wide range of pH 4–7. The maximum adsorption capacities obtained using the Langmuir model were 769.2, 833.3, and 909.1 mg g−1 at 10, 25 and 40 °C, respectively. At a dosing rate of 0.4 g L−1, MoS2B/CaCO3/Alg was able to reduce the Pb(II) concentration to below 0.05 ppm in complex simulated lead battery wastewater. After 10 repeated cycles, MoS2B/CaCO3/Alg maintained a high removal rate of 98.4 %. This spherical adsorbent is simple to prepare and easy to recover, has an ultra-high adsorption capacity, and is mechanically stable and resistant to interference, thus it is expected to be suitable for application in industrial wastewater treatment.
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| 21. |
- He, Zhuang, et al.
(författare)
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Microwave-assisted synthesis of amorphous cobalt nanoparticle decorated N-doped biochar for highly efficient degradation of sulfamethazine via peroxymonosulfate activation
- 2022
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Ingår i: Journal of Water Process Engineering. - : Elsevier. - 2214-7144. ; 50
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Tidskriftsartikel (refereegranskat)abstract
- In the present work, a microwave-assisted and secondary roasting preparation process was used to synthesize nanocomposite materials. These materials were modified with amorphous cobalt nanoparticles (Co NPs) on the surface of biochar doped with different nitrogen sources (melamine (Me), 1,10-phenanthroline (Ph), and urea (Ur)). The nanocomposite (Co-N-C(Ur)) with urea as the nitrogen source promoted the generation of mesopores on the surface of carbon materials due to its evaporation during the preparation process thus enhancing the attachment sites of cobalt nanoparticles. The Co-N-C(Ur) had a more significant degradation effect on the primary carcinogen sulfamethazine (SMT) by activating peroxymonosulfate (PMS). The degradation rate of SMT pollutants was 96.6 % within 30 min. The optimal reaction conditions were as follows: catalyst dosage of 0.4 g L−1, PMS dosage of 0.812 mM, SMT concentration of 10 mg L−1, and pH of 5.67. Additionally, the Co-N-C(Ur) catalysts possess excellent specific surface area due to the evaporation effect of the calcination process of urea itself compared to other nitrogen source doping. Electrochemical tests revealed that the composites prepared with urea as the nitrogen source had higher PMS-induced current density and lowered material impedance values, which effectively promoted the catalytic performance of SMT degradation. Concurrently, the Co-N-C (Ur) + PMS reaction system exhibited excellent catalytic performance against other antibiotic organic pollutants. Subsequently, through the capture experiments and electron paramagnetic resonance technical analyses, it was determined that the singlet 1O2 played a leading role in the reaction system. Finally, a thorough liquid chromatography-mass spectrometry analysis suggested the possible SMT degradation pathways, thereby providing a new strategy for the subsequent heterogeneous catalysts to degrade persistent organic pollutants.
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| 22. |
- Hong, Jie, et al.
(författare)
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A macroporous carbon nanoframe for hosting Mott-Schottky Fe-Co/Mo2C sites as an outstanding bi-functional oxygen electrocatalyst
- 2023
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Ingår i: Materials Horizons. - : Royal Society of Chemistry. - 2051-6347 .- 2051-6355. ; 10:12, s. 5969-5982
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Tidskriftsartikel (refereegranskat)abstract
- Simultaneously optimizing the d-band center of the catalyst and the mass/charge transport processes during the oxygen catalytic reaction is an essential but arduous task in the pursuit of creating effective and long-lasting bifunctional oxygen catalysts. In this study, a Fe-Co/Mo2C@N-doped carbon macroporous nanoframe was successfully synthesized via a facile “conformal coating and coordination capture” pyrolysis strategy. As expected, the resulting heterogeneous electrocatalyst exhibited excellent reversible oxygen electrocatalytic performance in an alkaline medium, as demonstrated by the small potential gap of 0.635 V between the operating potential of 1.507 V at 10 mA cm−2 for the oxygen evolution reaction and the half-wave potential of 0.872 V towards the oxygen reduction reaction. Additionally, the developed Zn-air battery employing the macroporous nanoframe heterostructure displayed an impressive peak power density of 218 mW cm−2, a noteworthy specific capacity of 694 mA h gZn−1, and remarkable charging/discharging cycle durability. Theoretical calculations confirmed that the built-in electric field between the Fe-Co alloy and Mo2C semiconductor could induce advantageous charge transport and redistribution at the heterointerface, contributing to the optimization of the d-band center of the nanohybrid and ultimately leading to a reduction in the reaction energy barrier during catalytic processes. The exquisite macroporous nanoframe facilitated the rapid transport of ions and charges, as well as the smooth access of oxygen to the internal active site. Thus, the presented unique electronic structure regulation and macroporous structure design show promising potential for the development of robust bifunctional oxygen electrodes.
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| 23. |
- Hong, Jie, et al.
(författare)
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Asymmetrically coupled co single-atom and co nanoparticle in double-shelled carbon-based nanoreactor for enhanced reversible oxygen catalysis
- 2023
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Ingår i: Chemical Engineering Journal. - : Elsevier. - 1385-8947 .- 1873-3212. ; 455
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Tidskriftsartikel (refereegranskat)abstract
- Simultaneous construction of size-asymmetric metal single atoms and nanoparticle active sites in advanced and robust carrier materials is particularly important yet challenging for efficient reversible oxygen catalysis. Herein, a facile “chemical etching/in-Situ capture” synthesis strategy was developed to fabricate a unique double-shelled carbon-based nanobox integrated with size-asymmetric Co single-atom (CoSA) and metallic Co nanoparticle (CoNP) moiety. As expected, this well-managed catalyst product yielded remarkable bifunctional electrocatalytic performances in alkaline electrolytes, with a decent half-wave potential of 0.886 V for oxygen reduction reaction (ORR) and a small overpotential of 341 mV at 10 mA/cm2 for oxygen evolution reaction (OER). Besides, this nanobox catalyst served as a cost-effective and efficient oxygen electrode in the assembled rechargeable ZABs, exceeding the mixed electrocatalyst of expensive Pt/C-RuO2, in terms of the elevated peak power density of 239 mW/cm2, the promoted specific capacity of 770 mAh/gZn, as well as the appreciable charge–discharge cycle stability. Theoretical calculations revealed that the strong interaction between the delicate CoSA site and CoNP phase, could effectively optimize the adsorption and desorption energy barriers of reaction intermediates on the designed catalyst surface, thus achieving synergistic enhancement of electrocatalytic activity towards ORR and OER. This finding affords a feasible and effective strategy to achieve highly active and durable bifunctional catalysts for both fundamental research and practical rechargeable ZABs applications.
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| 24. |
- Huang, Yimin, et al.
(författare)
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Facile synthesis of sodium lignosulfonate/polyethyleneimine/sodium alginate beads with ultra-high adsorption capacity for Cr(VI) removal from water
- 2022
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Ingår i: Journal of Hazardous Materials. - : Elsevier. - 0304-3894 .- 1873-3336. ; 436
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Tidskriftsartikel (refereegranskat)abstract
- Chromium (VI) is a widely occurring toxic heavy metal ion in industrial wastewater that seriously impacts the environment. In this study, we used environmentally friendly sodium lignosulfonate (SL), polyethyleneimine (PEI), and sodium alginate (SA) to synthesize SL/PEI/SA beads by employing a simple crosslinking method with to develop a novel absorbent with excellent adsorption capacity and practical application in wastewater treatment. We studied the adsorption performance of SL/PEI/SA through batch adsorption and continuous dynamic adsorption experiments. SL/PEI/SA has ultra-high adsorption capacity (2500 mg·g-1) at 25 ℃, which is much higher than that of existing adsorbents. Humic acids and coexisting anions commonly found in wastewater have minimal effect on the adsorption performance of SL/PEI/SA. In the column system, 1 g SL/PEI/SA can treat 8.1 L secondary electroplating wastewater at a flow rate of 0.5 mLmin-1, thereby enabling the concentration of Cr(VI) in secondary electroplating wastewater to meet the discharge standard (< 0.2 mg·L-1). It is worth noting that the concentration of competitive ions in secondary electroplating wastewater is more than 500 times higher than that of Cr(VI). These results demonstrate that the novel SL/PEI/SA beads can be effectively applied in the removal of Cr(VI) in wastewater.
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| 25. |
- Jia, Xiuxiu, et al.
(författare)
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Rod-shaped lanthanum oxychloride-decorated porous carbon material for efficient and ultra-fast removal of phosphorus from eutrophic water
- 2023
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Ingår i: Separation and Purification Technology. - : Elsevier. - 1383-5866 .- 1873-3794. ; 306
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Tidskriftsartikel (refereegranskat)abstract
- Removal of excess phosphorus (P) from water systems can effectively prevent eutrophication and maintain the ecological balance. In this study, we used a novel freeze-drying thermal oxidation process to prepare a rod-shaped lanthanum oxychloride decorated porous carbon material, polyvinylpyrrolidone /LaOCl (PL). PL showed excellent performance in removing P from water; the preparation method had not been reported previously. Specifically, the adsorption capacity of PL for P was as high as 90.9 mg P/g, and the removal rate was greater than 92.0 % over a wide pH range (2.5–11). Fast adsorption kinetics is an important feature for P removal. The high removal rate of PL for P could be achieved in a short time; that is, more than 97.8 % of the P species could be removed in only 25 min (initial concentration: 20 mg P/L). For water samples from the natural Laoyu River (24 μg P/L), 0.01 g of PL could reduce approximately 53 L of water to below the eutrophication threshold value (20 μg P/L). Furthermore, after five repetitions of the adsorption–desorption process, no significant decrease in the P removal efficiency was observed. The high adsorption capacity, fast adsorption kinetics, and persistent cyclic stability of PL for P in water were attributed to the advanced preparation process, in which freeze-drying ensured the porosity of the adsorbent and the uniformity of LaCl3 distribution; and the subsequent heat treatment created conditions for the generation of LaOCl species with stable adsorption activity. The adsorption mechanism mainly involved ion exchange, electrostatic attraction, and hydrogen bonding. This study provides a theoretical basis for preparing new adsorbing materials of P and technical support for preventing water eutrophication.
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