Processes
·
2022
·Vol. 10
·期 7
·1359
·
IF 3.352
Xiaoyu Huo,Chao Jia,Shanshan Shi,Tao Teng,Shaojie Zhou,Mingda Hua,Xiangdong Zhu,Shicheng Zhang,Qunjie Xu
Potassium thiocyanate (KSCN), a highly efficient “three birds with one stone” activator, might work with inorganic activators to produce excellent N/S co-doped porous carbon (NSC) materials for environmental remediation. However, the effects of inorganic activators on cooperative activation are unclear. As a result, the influence of inorganic activators on the synthesis of NSC materials was investigated further. This study shows that the surface areas of the NSC materials acquired through cooperative activation by potassium salts (KOH or K2CO3) were considerably higher than those acquired through KSCN activation alone (1403 m2/g). Furthermore, KSCN could cooperate with K2CO3to prepare samples with excellent specific surface area (2900 m2/g) or N/S content. The as-prepared NSC materials demonstrated higher adsorption capability for chloramphenicol (833 mg/g) and Pb2+(303 mg/g) (pore fitting, complexation). The research provides critical insights into the one-step synthesis of NSC materials with a vast application potential.Keywords:N/S co-doping;porous carbon;chloramphenicol adsorption;Pb2+removal
研究领域:
环境科学
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材料科学
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DOI
高影响因子
Journal of Materials Chemistry A
·
2024
·
IF 10.7
Zhengjie Su,Xinru Wu,Dong-Hau Kuo,Baoqian Yang,Binghong Wu,Longyan Chen,Pengkun Zhang,Jinguo Lin,Dongfang Lu,Xiaoyun Chen
Herein, an Ag/S co-doped Bi2O3-based sulfur oxide catalyst was prepared via a facile green method. The Ag/S–Bi2O3 catalyst with suitable Ag/S doping demonstrated super visible light photocatalytic hydrogen evolution (PHE) at 7.52 mmol g−1 h−1, with an apparent quantum efficiency (AQE) of 8.67% at 420 nm. Ag/S co-doping can adjust the energy band structure of an oxidation type Bi2O3 catalyst, converting it into a visible light hydrogen production catalyst suitable for hydrogen production. Sulfur doping adjusts the content of oxygen vacancies to enhance the surface active sites, and the introduction of noble metal silver endows the catalyst with more excellent electrical conductivity and electron trapping ability. Thus, Bi2O3 with Ag/S co-doping produced a suitable energy band structure, enhanced the content of oxygen vacancies and the number of surface active sites, and endowed the catalyst with excellent electrical conductivity and electron trapping ability, significantly producing catalysts with excellent visible light PHE activity. Furthermore, Ag/S–Bi2O3-3 exhibited super visible light PHE activity and excellent stability and persistence and is expected to play a potential role in the field of PHE reactions (PHERs).
研究领域:
材料科学
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催化化学
✓ 已验证
产品关联
DOI
高影响因子
Sustainability
·
2021
·Vol. 13
·期 15
·8255
·
IF 3.251
Jiaran Zhang,Zeyu Xu,Ce Shi,Xinting Yang
Excessive ammonia can cause the death of fish and the eutrophication of the water environment, so ammonia detection is essential for environmental monitoring. In this study, a highly selective sensing strategy for ammonia detection based on N, S co-doped carbon dots (N, S-CDs) was developed. The as-prepared N, S-CDs exhibited excellent photoluminescence properties and fluorescent stability. N, S-CDs demonstrated fluorescence quenched in the presence of ammonia in the wide linear range of 2–80 mmol/L, and were highly selective towards ammonia over metal ions. Furthermore, a possible fluorescence quenching mechanism is proposed. N, S-CDs were further applied to detection of ammonia in aquaculture water samples and river water samples, showing good practicability with recoveries from 0.93 to 1.27 and relative standard deviations (RSDs) of 0.54% to 17.3%. N, S-CDs were also successfully used to determine the freshness of bighead carps.Keywords:carbon dots;fluorescence;ammonia;aquaculture;freshness
研究领域:
环境科学
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分析化学
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水产养殖
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Jiawen Yan,Ke Sang,Xiaohan Jiang,Qiming Li,Fuyi Jiang,Yanli Zhou
In this study, amorphous MoS 3 -modified porous Co 4 S 3 -embedded N,S co-doped carbon polyhedron (Co 4 S 3 @NSC/MoS 3 ) was rationally prepared via a multi-step method. One-dimensional linear-like MoS 3 with a high specific capacity of 894 mAh g −1 and abundant active sites compensated for the low capacity of Co 4 S 3 , thus enhancing the sodium ion storage capacity of the entire electrode. Moreover, three-dimensional N,S co-doped carbon networks (NSC) significantly inhibited large volumetric fluctuations in Co 4 S 3 and MoS 3 , thereby sustaining the structural stability and enhancing the electron transfer efficiency. As a new anode material for sodium-ion half batteries, the constructed Co 4 S 3 @NSC/MoS 3 with rapid Na + diffusion and charge transfer kinetics demonstrated better sodium storage properties than Co 4 S 3 @NSC. At a rate of 0.5 A g −1 over 100 cycles, the reversible specific capacity of Co 4 S 3 @NSC/MoS 3 reached 594 mAh g −1 . Even when cycled at a rate of 2 A g −1 for 600 cycles, the charge capacity was stable at 435 mAh g −1 . The rate performance of Co 4 S 3 @NSC/MoS 3 was also found to be remarkable; when the rate increased to 10 A g −1 , the average capacity was retained at 382 mAh g −1 . Apart from half cells, reduced graphene oxide (rGO)-modified Na 3 V 2 (PO 4 ) 3 composite (Na 3 V 2 (PO 4 ) 3 @rGO) was used as the cathode material to match with Co 4 S 3 @NSC/MoS 3 . The assembled full batteries were analyzed and their electrochemical properties were discussed. They also exhibited outstanding rate capability and high-rate long-life cyclic property. Even at 1 A g −1 over 500 cycles, the discharge capacity was stably maintained at 246 mAh g −1 . The outstanding sodium storage properties of Co 4 S 3 @NSC/MoS 3 mainly depended on the cooperative effects of MoS 3 and Co 4 S 3 @NSC, indicating the potential application of Co 4 S 3 @NSC/MoS 3 in energy storage fields.
研究领域:
材料科学
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能源存储
✓ 已验证
产品关联
DOI
PubMed
高影响因子
MATERIALS CHEMISTRY AND PHYSICS
·
2025
·
IF 4.7
Xiaoxu Cui,Zherui Wan,Zhonghao Li,Fengxia Wang,Pengshuai Wei,Guang Yang
Herein, intelligent N, S-doped fluorescent carbon dots (N, S-CDs) were constructed by using l -cysteine and carboxymethyl cellulose (CMC) polymer as precursors through a one-step hydrothermal method. The designed N, S-CDs displayed strong fluorescence (FL) emission with a FL quantum yield of 44.48 % and could be utilized for the quantitative tracing of TCs and Al 3+ via the “On-OFF-ON” FL transition with wide linear detection range (1.66–104.5 μM for TCH, 1.66–163.2 μM for OTC, 1.66–69.5 μM for DOX and 33–104.3 μM for Al 3+ ). The detection limits (LODs) of TCH, OTC, DOX and Al 3+ were calculated to be 53.02 nM, 95.61 nM, 41.87 nM and 57.69 nM, respectively. On the basis of the FL “On-OFF-ON” strategy, multiple logical gate operations including “NOR” and “INHIBIT”, were constructed successfully. Additionally, N, S-CDs uploaded to hydrogen bars were utilized for the recognition of TCs and Al 3+ in a portable manner, which revealed great application potential in the field of anti-counterfeiting and encryption.
研究领域:
分析化学
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材料科学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
Journal of Materials Chemistry A
·
2014
·Vol. 2
·期 33
·13565-13570
·
IF 0
Yingying Fan,Dongxue Han,Bin Cai,Weiguang Ma,Mohsin Javed,Shiyu Gan,Tongshun Wu,M. Siddiq,Xiandui Dong,Li Niu
TiO2 is an abundant and environmentally benign material, but has a wide band gap, which greatly confines its applications in photocatalysis. Doping and modifying the material composition are both generally used to change and control the photocatalytic activity of semiconductors. Herein, we describe a method and resulting activity of depositing Ce-/S-codoped TiO2 nanoparticles (NPs) on water-soluble sulfonated graphene (SGE) sheets, which guarantees a direct contact and satisfactory electron transfer between the semiconductor and graphene. The Ce/S–TiO2 NPs are homogeneously fixed on the surface of SGE sheets with an average particle size of ∼7 nm. The resulting composite showed noticeable activity in photodegrading methyl orange (κ = 0.425 h−1). This improved performance can be attributed to the synergistic effects of Ce- and S-codoping toward TiO2 and the composite action between TiO2 NPs and SGE. This type of novel composite is expected to stimulate the development of doped and graphene-involved photocatalysts for addressing environmental problems.
研究领域:
材料科学
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环境科学
✓ 已验证
产品关联
DOI
JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2024
·
IF 9.4
Xiaobo Wang,Zhengqiu He,Kaixuan Huo,Jialiang Liu,Qingshan Zhao,Mingbo Wu
Constructing high-performance and low-cost carbon anodes for potassium-ion batteries (PIBs) is highly desirable but faces great challenges. In this study, we present a novel approach to fabricating N/S co-doped hollow amorphous carbon (LNSHAC) for superior potassium storage through a template-assisted molecular structure regulation strategy. By tailoring a 3D crosslinked aromatics precursor from fluid catalytic cracking slurry (FCCs), the LNSHAC features a N/S co-doped hollow structure with enlarged interlayer spacing of up to 0.405 nm and rich defects. Such unique microstructure offers fast transport channels for K-ion intercalation/deintercalation and provides more active sites, leading to boosted reaction kinetics and potassium storage capacity. Consequently, the LNSHAC electrode delivers an impressive reversible capacity (466.2 mAh g −1 at 0.1 A/g), excellent rate capability (336.3 mAh g −1 at 2 A/g), and superior cyclic performance (256.9 mAh g −1 after 5000 cycles at 5 A/g with admirable retention of 76.9 %), standing out among the reported carbon-based anodes. When KFeHCF is employed as the cathode, the LNSHAC-based K-ion full cell exhibits a high reversible capacity of 176.6 mAh g −1 at 0.1 A/g and excellent cyclic stability over 200 cycles. This work will inspire the development and application of advanced carbon-based materials for potassium electrochemical energy storage.
研究领域:
材料科学
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电化学能源存储
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SYNTHETIC METALS
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2021
·
IF 3.266
Jiaoyan Shi,Lipeng Wu,Qingya Sun,Fan Wu,Aming Xie
Elemetal doping is an efficient strategy to adjust the microstructue and electronic property of a carbon material, as a result, shows great potential in the design of novel electromagnetic absorption (EMA) materials. In this work, we report an useful strategy to prepare a N,S co-doped carbon (NSC) using TTF-TCNQ as the precusor, and systematically explore its frequency-depedent dielectric and EMA properties. Different N/S ratios can be tuned by the regulation of pyrolitic temperature. The derived NSC exhibits wonderful EMA performance when the pyrolytic temperature is setted to 700 ℃ with loading ratio of 35 wt%. Efficient absorption can be achieved in the frequency range of 6.4–18 GHz. Moreover, it is determined that the efficient absorption bandwidth gets to 6.5 GHz, while the maximal absorption reaches −46 dB. The EMA mechanism of NSC is considered to be mainly contributed by improved impedance matching realized by macropores, enhanced conductance loss caused by well constructed condutive network, and polarization by N,S doping. This research provides a new idea for development of novel carbon materials for EMA applicaion.
研究领域:
材料科学
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电磁学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
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2023
·
IF 6.2
Zhentao Bian,Meng Li,Taoqin Liu,Chengcheng Liu,Yanyan Zhu,Hongxia Cao,Guang Zhu,Hongyan Wang,Chong Chen,Keying Zhang
Recent research interest has increased in the production of heteroatoms-doped porous carbon with controlled morphology from biomass. However, there is still a significant challenge in resolving alkaline solutions that cause equipment corrosion and devising a simple and adaptable approach. In this study, N/O/S co-doped honeycomb-like porous carbons were synthesized from a widely cultivated annual weed ( Hemistepta Iyrata Bunge ) using a simple and eco-friendly method. The sodium hydroxide (NaOH)/urea system was utilized as the pore-forming agent and cellulose solvent, with urea as the nitrogen source. By varying the activation temperature, the as-prepared porous carbon has a high specific surface area (709 m 2 g −1 ), a large total pore volume (0.44 cm 3 g −1 ), and a high heteroatom content of 6.20 at% nitrogen and 8.12 at% oxygen. The prepared porous materials were evaluated as electrodes for supercapacitors . The product (HIB-PHC-750 °C) exhibited a high specific capacitance (353.6 F g −1 at 0.2 A g −1 ) at a carbonization temperature of 750 °C. Additionally, the HIB-PHC-750 °C-based symmetric device with a wide voltage range of 2.0 V possessed a desirable energy density of 44.22 Wh kg −1 at 500 W kg −1 . Moreover, the HIB-PHC-750 °C also demonstrated outstanding cycling stability with 98.2 % capacitance retention after 10,000 cycles. This research provided a facile and favorable alternative method for preparing N/O/S co-doped honeycomb-like porous carbon for electrochemical energy storage devices.
研究领域:
材料科学
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能源存储
·
生物质利用
✓ 已验证
产品关联
DOI
高影响因子
ChemCatChem
·
2017
·Vol. 10
·期 4
·796-803
·
IF 4.803
Shi Feng,Xingyue Li,Jia Huo,Qiling Li,Chao Xie,Tingting Liu,Zhigang Liu,Zhenjun Wu,Shuangyin Wang
Graphical Porous carbon electrode : CoS 2 @N/S-codoped porous carbon is prepared through an electrodeposition–ZIF conversion–sulfuration strategy. The loading of active sites can be controlled easily by varying the electrodeposition time. The resulting material can be employed directly as a working electrode for the hydrogen evolution reaction and shows an excellent catalytic activity and stability. A convenient, controllable method to fabricate an electrode is necessary to achieve the practical application of a hydrogen evolution reaction (HER) catalyst. In this work, an electrodeposition–ZIF conversion–sulfuration strategy is developed to produce a CoS 2 @N/S-codoped porous carbon (CoS 2 @NSC/CFP) to drive the HER efficiently. CoS 2 @NSC/CFP was prepared by the electrodeposition of Co(OH) 2 on a carbon fiber paper followed by conversion into ZIF-67 and subsequent sulfuration with sulfur. The loading of electroactive components can be controlled easily in the range of 0.7–10.0 mg cm −2 by varying electrodeposition time from 5 min to 2 h. The resulting material can be employed directly as a working electrode for the HER and it shows an excellent catalytic activity and stability with an overpotential of 95 mV at 10 mA cm −2 and 158 mV to reach 100 mA cm −2 in an acidic medium. The high efficiency is related intimately to the high dispersion of ultra-small CoS 2 nanoparticles, heteroatom-codoping, and the 3 D porous network configuration of the carbon fiber paper.
研究领域:
材料科学
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电化学
✓ 已验证
DOI
高影响因子
Nanomaterials
·
2022
·Vol. 12
·期 12
·2079
·
IF 5.719
Dong Li,Fachao Wu,Caiyun Gao,Hongfang Shen,Fei Han,Fenglan Han,Zhanlin Chen
In this work, a highly efficient wide-visible-light-driven photoanode, namely, nitrogen and sulfur co-doped tungsten trioxide (S-N-WO3), was synthesized using tungstic acid (H2WO4) as W source and ammonium sulfide ((NH4)2S), which functioned simultaneously as a sulfur source and as a nitrogen source for the co-doping of nitrogen and sulfur. The EDS and XPS results indicated that the controllable formation of either N-doped WO3(N-WO3) or S-N-WO3by changing the nW:n(NH4)2Sratio below or above 1:5. Both N and S contents increased when increasing the nW:n(NH4)2Sratio from 1:0 to 1:15 and thereafter decreased up to 1:25. The UV-visible diffuse reflectance spectra (DRS) of S-N-WO3exhibited a significant redshift of the absorption edge with new shoulders appearing at 470–650 nm, which became more intense as the nW:n(NH4)2Sratio increased from 1:5 and then decreased up to 1:25, with the maximum at 1:15. The values of nW:n(NH4)2Sratio dependence is consistent with the cases of the S and N contents. This suggests that S and N co-doped into the WO3lattice are responsible for the considerable redshift in the absorption edge, with a new shoulder appearing at 470–650 nm owing to the intrabandgap formation above the valence band (VB) edge and a dopant energy level below the conduction band (CB) of WO3. Therefore, benefiting from the S and N co-doping, the S-N-WO3photoanode generated a photoanodic current under visible light irradiation below 580 nm due to the photoelectrochemical (PEC) water oxidation, compared with pure WO3doing so below 470 nm.Keywords:N, S co-doped;water oxidation;tungsten trioxide;photoanode;photoelectrochemical;water splitting
研究领域:
材料科学
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光化学
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电化学
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可再生能源
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Jiarun Cheng,Chaojie Lyu,Hongming Chen,Dongsheng Geng,Jinlong Zheng
Elucidating the mechanism of metal-support interface domain regulation is crucial for designing efficient fuel cell electrocatalysts. Herein, we propose an emerging strategy to enhance oxygen reduction reaction (ORR) activity and selectivity by regulating the Lewis alkalinity of carbon support to adjust the Lewis acidity of metal sites. The experimental results and density functional theory (DFT) simulations show that the introduction of N/S atoms into the carbon support structure will break the charge balance of the carbon skeleton and effectively regulate the charge distribution in the Pt-carbon interface domain, thus promoting the oxidation of the Lewis acid Pt atoms to a higher valence state Pt x+ , so as to optimize the adsorption energy of oxygen-containing intermediates. Moreover, Bader charge analysis also verifies that N,S-HMCS, as a Lewis base, can receive more electrons from the Pt sites of Lewis acid, and the electron loss at Pt sites caused by N,S-HMCS strengthens interfacial electron effect. Meanwhile the strong electron adsorption ability of N/S atoms causes the d-band center of Pt atom orbital to shift upward to the Fermi level, which strengthens the binding of metal Lewis acid Pt sites with *OOH intermediates, and improves the 4-electron transfer mechanism. This research reveals the direct role of Lewis acid sites in ORR of fuel cell cathode, and provides a feasible way to guide the design of electrocatalysts with Lewis acid/base double centers.
研究领域:
材料科学
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电化学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）