ACS Omega
·
2021
·
IF 3.512
Qirui Guo,Chong Chen,Fangcheng Xing,Weizhong Shi,Jie Meng,Hui Wan,Guofeng Guan
Nitrogen-doped hierarchical porous carbons with a rich pore structure were prepared via direct carbonization of the poly(ionic liquid) (PIL)/potassium ferricyanide compound. Thereinto, the bisvinylimidazolium-based PIL was a desirable carbon source, and potassium ferricyanide as a multifunctional Fe-based template, could not only serve as the pore-forming agent, including metallic components (Fe and Fe3C), potassium ions (etching carbon framework during carbonization), and gas generated during the pyrolysis process, but also introduce the N atoms to porous carbons, which were in favor of CO2 capture. Moreover, the hierarchically porous carbon NDPC-1-800 (NDPC, nitrogen-doped porous carbon) had taken advantage of the highest specific surface area, exhibiting an excellent CO2 adsorption capacity and selectivity compared with NDC-800 (NDC, nitrogen-doped carbon) directly carbonized from the pure PIL. Furthermore, its hierarchical porous architectures played an important part in the process of CO2 capture, which was described briefly as follows: the synergistic effect of mesopores and micropores could accelerate the CO2 molecules’ transportation and storage. Meanwhile, the appropriate microporous size distribution of NDPC-1-800 was conducive to enhancing CO2/N2 selectivity. This study was intended to open up a new pathway for designing N-doped porous carbons combining both PILs and the multifunctional Fe-based template potassium ferricyanide with wonderful gas adsorption and separation performance.
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高影响因子
ACS Applied Energy Materials
·
2022
·
IF 6.959
Chi Wei,Gaoxu Huang,Jiayi Mao,Jia Cai,Xiaopan Jin,Mengjia Guan,Feng Yu,Bin Dai,Yongsheng Li
Sodium metal batteries (SMBs) are attracting intensive attention as an appealing candidate for high-energy-density batteries, owing to the high specific capacity, rich abundance, and low cost of metallic sodium (Na). However, the practical application of SMBs has been greatly hindered by the uncontrollable dendrite growth and unstable solid electrolyte interfaces, which are responsible for the poor Na stripping/plating reversibility and short lifespan. Herein, we report an atomically dispersed Fe-doped mesoporous carbon nanosphere (Fe-MCN) as a sodiophilic host for facilitating homogeneous Na nucleation and deposition behaviors. Benefitting from the advantages of uniform mesoporous structures with large surface areas and atomically dispersed Fe doped in the carbon nanospheres, low nucleation barriers and subsequent homogeneous deposition behavior of Na metal are achieved, which give rise to highly reversible stripping/plating performance and outstanding cycling stability. As a result, the Na||Cu cell based on Fe-MCN-modified Cu substrates exhibits outstanding electrochemical performance with a high Coulombic efficiency of 99.97% over 850 cycles, and an ultralong cycling lifespan of 2600 h at 1 mA cm–2 and 1 mA h cm–2 is demonstrated by the symmetric cell with Na@Fe-MCN@Cu anodes. Moreover, the Na3V2(PO4)3 full cell based on the Na@Fe-MCN@Cu anode guarantees outstanding cycling stability for 2000 cycles with a capacity retention as high as 84%, showing high potential in the practical application of SMBs.
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高影响因子
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
·
2024
·Vol. 27
·期 24
·e202400196
·
IF 2.2
Wenkang Mao,Jinjing Ju,Dan Li,Daishe Wu,Feigao Xu
Graphical Synopsis: A pyrrolic N-rich g-C 3 N 4 (PN-g-C 3 N 4 ) framework is synthesized with transition metal M (M=Fe, Co, Ni, Cu, Cr, and Mn) atomic sites coordinated onto it. M/PN-g-C 3 N 4 are constructed for peroxodisulfate activation. The synergy between photocatalysis and Fe/PN-g-C 3 N 4 catalyst results in increased generation and separation of charge carriers, along with the cyclic transformation of the Fe 3+ /Fe 2+ couple. Photocatalysis is an efficient technology for the degradation of pollutants. However, there is still much room for improvement in its degradation efficiency. In this study, a pyrrolic N-rich g-C 3 N 4 (PN-g-C 3 N 4 ) framework was synthesized with transition metal M (M=Fe, Co, Ni, Cu, Cr, and Mn) atomic sites coordinated onto it. Then, a series of single atomic metals M anchored to PN-g-C 3 N 4 (M/PN-g-C 3 N 4 ) are constructed for peroxodisulfate activation. Their order of catalytic activity follows Fe>Cr>Ni>Cu≈Co>Mn, in particular the degradation rates of the TCH for Fe-PN-g-C 3 N 4 are 3.74 times higher than that of undoped PN-g-C 3 N 4 . These carefully regulated pyrrolic N-rich Fe sites demonstrate outstanding performance in degrading organic pollutant. As an exemplary model, the Fe/PN-g-C 3 N 4 catalyst efficiently drives the catalytic oxidation of TCH through Fenton-like reaction under visible light, showcasing exceptional cycle stability and a broad effective pH range of 3.0–11.0. The synergy between photocatalysis and Fe doped catalysis results in increased generation and separation of charge carriers, along with the cyclic transformation of the Fe 3+ /Fe 2+ couple. This combination significantly enhances the Fenton-like performance, making it a highly effective process for pollutant degradation.
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高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2024
·
IF 8.1
Tong-hui Yang,Song Yue,Wei-wei Gong,Ren-qing Wang,Wei-da Hu,Xiao-pan Liu,Peng-zhao Gao,Hang Qin,Wen-ming Guo,Han-ning Xiao
Electrochemical nitrogen reduction reaction(eNRR) is a promising strategy for ammonia production because of its mild reaction conditions, high theoretical conversion rate, and green pollution. However, the strong stability of N N triple bond and competitive hydrogen evolution reaction (HER) limit the Faraday efficiency and ammonia conversion of eNRR. In recent years, the structural design of catalysts combined with external field enhancement to enhance the AC magnetic field electrocatalytic reaction has received extensive attention. In this study, an eNRR catalyst ( x Fe-M-TiO 2 ) with a high concentration of oxygen vacancies was constructed by the defect engineering strategy. The ammonia conversion rate of eNRR of 1.5Fe-M-TiO 2 was 7.35 μg h −1 mg cat −1 , and the Faraday efficiency was 22.69 %, which was 2 % higher than that before doping. The spin–orbit coupling effect induced by the AC magnetic field further improved the eNRR activity, in which the Faraday efficiency increased to 52.14 % (increased by 150 %), and the ammonia yield increased to 13.37 μg h −1 mg cat −1 (increased by 5 %). After 80 h of eNRR, the current density of the catalyst became 95 % of the initial current density, and the stability was good. Density functional theory calculation showed that Fe doping did not change the reaction mechanism of eNRR but increased the concentration of oxygen vacancy, resulting in a 0.62 eV decrease in the energy barrier of the first hydrogenation of eNRR, which was conducive to the occurrence of eNRR.
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JOURNAL OF ENVIRONMENTAL ENGINEERING
·
2023
·Vol. 149
·期 9
·04023052
·
IF 2.2
Xincheng Ye,Jie Yao,Zekun Dong,Yan Zhang
The novel Fe-doped MoS2/granulated activated carbon (GAC) particle electrodes (FMG PEs) were controllably synthesized by a hydrothermal method and used in the three-dimensional (3D) electroactivation of peroxydisulfate (E-PDS-FMG) for carbamazepine (CBZ) degradation. The performance, mechanism, and influencing factors of CBZ degradation by the E-PDS-FMG system were systematically discussed. Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) analyses showed that the E-PDS-FMG system has an excellent conductivity and a high electron transfer rate and exhibited a superior electrocatalytic performance for CBZ degradation. A CBZ removal rate greater than 99% can be achieved within 25 min under the conditions of FMG dosage of 0.4 g L−1, PDS concentration of 2.0 mM, current density of 1.0 mA cm−2, and initial pH value of 5. Sulfate radicals (SO4·−) and hydroxyl radicals (OH) were recognized as the major active species through quenching experiments and electron paramagnetic resonance (EPR) measurement. In addition, Fe (IV) was also involved in the E-PDS-FMG system according to the transformation of methyl phenyl sulfoxide (PMSO) to methyl phenyl sulfone (PMSO2). Furthermore, the possible mechanism of the E-PDS-FMG system was proposed. FMG PEs were applied as the catalyst and particle electrodes for PDS activation, improving the yield of OH, SO4·−, and Fe (IV). The increase of FMG dosage and PDS concentration accelerated the degradation of CBZ, and the E-PDS-FMG system exhibited a high degradation ability on CBZ removal in a wide pH range. The results all indicate that the E-PDS-FMG system is a promising technology for organic pollutant removal from water due to its excellent electrocatalytic performance and remarkable stability.
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高影响因子
Journal of Energy Chemistry
·
2022
·
IF 13.599
Yuelong Xu,Ran Wang,Jingyue Wang,Yaru Zhang,Tifeng Jiao
Hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR) serve as the most promising electrochemical processes for renewable energy. Developing multifunctional electrocatalysts with high performance for HER, OER and ORR still remains a challenge. Herein, we report a facile method to prepare P, N-co-doped porous carbon encapsulated Fe-CoP (A-Fe-CoP/CPN) electrocatalyst through freeze drying, carbonization, and KOH activation. The acquired A-Fe-CoP/CPN possesses abundant pores with large surface area, which provides sufficient defect-rich sites for HER, OER, and ORR, in alkaline or acidic electrolytes. The A-Fe-CoP/CPN shows low overpotential and good stability for HER and OER in alkaline electrolyte. Density functional theory (DFT) computations reveal that the addition of Fe greatly facilitates the rate-determining step and overall catalytic pathway for both HER and OER. A-Fe-CoP/CPN also exhibits low half-wave potential ( E 1/2 ) for ORR, which indicates an enhanced performance than that of the noble Pt/C catalyst. Zn-air battery equipped with the A-Fe-CoP/CPN catalyst exhibits a high energy density (849 mAh g −1 ) and a long-time stability at 5 mA cm −2 . This finding not only offers a facile strategy to prepare porous carbon materials with defect-rich sites, but also provides guidance for developing multifunctional electrocatalysts for wide electrochemical reactions.
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高影响因子
Frontiers in Chemistry
·
2022
·
IF 5.545
Huo Zhaohui,Liao Yanmin,He Yongyi,Zhang Yifan,Liao Xiaolin,Zhang Qitong,Wu Haojie,Shi Junjie,Wen Genglong,Su Haixia,Yao Suyang
Graphitic carbon nitride (g-C3N4) has shown to be a promising photocatalyst that, however, suffers from strong charge recombination and poor conductivity, while MXenes have shown to be perfect cocatalysts for the photocatalytic process but show poor stability. In this study, we successfully constructed 2D/2D heterojunctions of Fe-C3N4/Ti3C2 for the photocatalytic degradation of antibiotics. In this study, multilayer Ti3C2 was obtained by etching Ti3AlC2, and then Fe-C3N4/Ti3C2 photocatalyst was prepared by the one-pot microwave method and high-temperature calcination method. The synthesized samples were characterized by XRD, SEM, TEM, XPS, TGA, BET, DRS, PL, and other means. The photocatalytic degradation of tetracycline hydrochloride by Fe-C3N4/Ti3C2 was in accordance with the first-order reaction kinetics model, and the apparent rate constant k was 2.83, 2.06, and 1.77 times that of g-C3N4, Fe-C3N4, and g-C3N4/Ti3C2, respectively. Through the mechanism study, it was shown that the most active species in the reaction system was • O2−, while h+ and •OH had a relatively lower effect on the degradation system.
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高影响因子
Chemical Engineering Journal Advances
·
2023
·
IF 0
Mengsi Cheng,Ying Fang,Zhaoguang Yang,Xinghao Liu,Bo Qiu,Tong Zhang,Haipu Li,Wenbo Zhao
MIL-100(Fe) was modified by amino groups (MIL - 100(Fe) - NH 2 ) to enhance the removal of antimonate (Sb(V)) with low concentration (50−200 μg/L) from natural water through batch adsorption experiments. With the initial Sb(V) concentration up to 200 μg/L, the residual Sb(V) concentration after treated by MIL - 100(Fe) - NH 2 was only 3.52 ± 0.131 μg/L, lower than the drinking water standards (5 μg/L) in China, while that was much higher (94.2 ± 3.52 μg/L) after pristine MIL-100(Fe) treatment. Based on results of XPS analysis, and adsorption kinetics and isotherms, we concluded that Sb(V) substituted the terminal −OH groups of MIL-100(Fe) to form inner-sphere complexes by coordination reactions with Fe nodes and be adsorbed by hydrogen bonding as well. The grafted amino groups (−NH 2 ) adsorbed Sb(V) by hydrogen bonding and facilitated the coordination reactions between Sb(V) and Fe nodes. The higher K L value (0.0116 ± 0.00,118 L/μg) obtained by fitting with the Langmuir isotherm model, while that of unmodified MIL-100(Fe) was 4.74 × 10 −4 ± 5.85 × 10 −5 L/μg, also confirmed that the −NH 2 groups greatly enhanced the affinity between MIL-100(Fe) and Sb(V). Furthermore, MIL - 100(Fe) - NH 2 still worked nicely in a wide pH range (2 − 12), with varied ionic strength (0.05 µmol/ L −1.5 mol/L), coexisting ions (CO 3 2− , NO 3 − , SO 4 2− , Cl − , H 2 PO 4 − ), and even in the real water bodies. Additionally, MIL - 100(Fe) - NH 2 exhibited good reusability and low Fe leaching (99.92 μg/L). We hope MIL - 100(Fe) - NH 2 become a candidate for effective removal of Sb(V), even other heavy metals from natural waterbodies.
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ENERGY & FUELS
·
2022
·
IF 4.654
Jing Li,Suxia Ma,Rongji Cui,Nuo Xu,Ting Pei
Solid waste fly ash can encroach on land, contaminate the environment, and jeopardize human health. An alkali fusion method combined with a hydrothermal method was adopted to prepare fly ash-derived ZSM-5 molecular sieves, and a series of Fe/ZSM-5 catalysts were also prepared to test their catalytic performance in NO oxidation with H2O2. Moreover, the characteristics of catalysts synthesized by fly ash, as well as the relationship between the structure and the catalytic activity, were analyzed in detail through multiple characterization approaches. The results gave important insights into the active sites of catalytic oxidation. They concluded that 10% Fe/ZSM-5 had the best catalytic activity in which Fe sites and Brønsted acid sites collectively provided the catalytic functionality, and 92% NO removal efficiency was obtained achieved under optimal experimental conditions. This work provided a new way for recycling fly ash and developing low-cost catalysts for NO removal.
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高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2015
·Vol. 27
·期 2
·1966-1973
·
IF 1.569
Lu Changyu,Guan Weisheng,Hoang Tuan K. A.,Guo Jifeng,Gou Haigang,Yao Yiliang
In this work, Fe-series (Fe, Co, Ni) doped titanate nanotubes were synthesized via a simple, one pot hydrothermal process using commercial TiO 2 powder as the precursor. The samples were characterized by X-ray diffraction, nitrogen adsorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy, and UV–Vis. SEM and TEM results show that regularly uniform nanotubes were obtained and they possess homogeneous tubular structures with open ends. There is no significantly morphological and structural difference between TiNTs and Fe-series doped TiNTs. Furthermore, the photocatalytic properties of TiNTs and Fe-series doped TiNTs were studied using the degradation of ciprofloxacin. Fe-series doped TiNTs exhibit higher catalytic activities than those of TiNTs and commercial TiO 2 .
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高影响因子
CHINESE JOURNAL OF CHEMICAL ENGINEERING
·
2020
·
IF 2.627
Shenglai Li,Lisong Fan,Lina Song,Dangguo Cheng,Fengqiu Chen
Iron-containing zeolites play an important role in the selective oxidation of methane to oxygenates by nitrous oxide. A solid-state ion exchange method is adopted to prepare Fe-MOR zeolite catalysts with different amounts of extra-framework Al. EPR spectra and UV–vis spectra show that the percentage of iron ions in tetrahedral or octahedral coordination increases while those of clustered Fe species decrease by the addition of extra-framework Al species. Nitrous oxide titration reveals that more active Fe centers are formed, which promote the nitrous oxide consumption. The number of active centers in the catalyst with the introduction of extra-framework Al is about four times that of the catalyst without the addition of extra-framework Al. Due to this, there is an increase in the methane conversion, total selectivity and yield of oxygenates.
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2019
·
IF 5.107
Yuqi Cui,Li-chao Nengzi,Jianfeng Gou,Yan Huang,Bo Li,Xiuwen Cheng
Z-scheme heterojunction photocatalyst can simultaneously reduce the recombination of photo-generated electron-hole pairs and preserve its outstanding redox ability during the process of photocatalytic reaction. In this study, Z-scheme MIL-53(Fe)/α-Bi 2 O 3 /g-C 3 N 4 photocatalyst was successfully fabricated via an accessible method and comprehensive characterized by XRD, FT-IR, SEM, TEM, XPS, N 2 adsorption-desorption isotherms, UV–vis diffuse reflection spectroscopy and photoelectrochemical analysis. The as-obtained MIL-53(Fe)/α-Bi 2 O 3 /g-C 3 N 4 composite exhibited superior photocatalytic activity for amino black 10B degradation than that of pure g-C 3 N 4 , α-Bi 2 O 3 , MIL-53(Fe) and α-Bi 2 O 3 /g-C 3 N 4 binary composite under visible light irradiation and the photodegradation rate would achieve the maximum when the mass fraction of MIL-53(Fe) was 32% in ternary composite. The enhanced photocatalytic performance of MIL-53(Fe)/α-Bi 2 O 3 /g-C 3 N 4 ternary composite could be mainly ascribed to improved visible light absorption range and the construction of an effective interfacial heterojunction driven by direct solid-state dual Z-scheme mechanism, which significantly facilitates the separation and transfer of photo-generated charge carriers. Eventually, the as-prepared ternary composite was confirmed to have prominent stability and reusability after consecutive 4 recycling run.
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高影响因子
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