IEEE ELECTRON DEVICE LETTERS
·
2023
·Vol. 44
·期 7
·1152-1155
·
IF 4.9
Weishuai Duan,Zhe Liu,Xinfa Zhu,Biao He,Chao Fan,Yonghui Zhang,Mengjun Wang,Hongxing Zheng,Erping Li
Near-ultraviolet (NUV) detectors based on two-dimensional (2D) materials have garnered considerable attention owing to their atomic-scale thickness, varied bandgap, and strong interaction with incident light. In this work, homostructures composed of tin disulfide/chromium–doped tin disulfide (SnS
2
/Cr–SnS
2
) were proposed for 405 nm near-ultraviolet detectors. Afterward, superlative detectors were fabricated through the employment of micro-mechanical exfoliation and polydimethylsiloxane-assisted dry-transfer methods, anchored by the SnS
2
Cr–SnS
2
homostructures. The detectors demonstrated exceptional detection performance for 405 nm NUV radiation with a significant responsivity of
$2.04\times 10^{{3}}\,\,\text {A}\cdot \text {W}^{-{1}}$
and a short response time of 8 ms, exceeding that of detectors based on most 2D materials and even commercial light detectors (Thorlabs FD11A–Si). The work presents an effective homostructure for high-performance SnS
2
-based detectors, thereby opening an opportunity for the utilization of SnS
2
in NUV detectors.
✓ 已验证
DOI
高影响因子
CARBOHYDRATE POLYMERS
·
2012
·
IF 3.628
Ke Zhang,Zhengke Wang,Youliang Li,Zhiqiang Jiang,Qiaoling Hu,Minying Liu,Qingxiang Zhao
In order to develop stimuli-responsive hydrogel, chitosan graft copolymer with chitosan back-bone and poly( N -isopropylacrylamide)- block -poly(acrylic acid) (PNIPAAm- b -PAA) branch chains was prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization in DMF. The chain transfer agent was obtained by modification of chitosan with 3-benzylsulfanyl thiocarbonylsulfanyl propionic acid (BPATT) with 68% the degree of substitute. The graft polymerizations possessed controlled/living characteristics. The behavior of the graft copolymer in aqueous solution was investigated by dynamic light scattering, transmission electron microscopy, and UV-visible spectrophotometer. N -Phthaloylchitosan- graft -(poly( N -isopropylacrylamide)- block -poly(acrylic acid)) copolymer ( N -phthaloylchitosan- g -(PNIPAAm- b -PAA)) could assemble to micelles in aqueous solution in range of 200–300 nm with narrow size distribution, and the hydrodynamic diameter could be controlled dependent on length of branch chains and temperature. The LCST values of micelle could be modulated from 34 to 40 °C by controlling the constitution of branch chains, pH, and concentration.
✓ 已验证
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Fangshuo Jia,Yujuan Zhang,Xiaolong Ma,Zihao Zheng,Fuqiang An,Tuoping Hu
Water electrolysis coupling methanol oxidation is an energy-efficient hydrogen generation technology, while obtaining high-value formic acid, however, superior catalysts are often required to achieve efficient hydrogen production. Herein, the n - n heterojunction (NiCo 2 S 4 -MoS 2 ) composed of NiCo 2 S 4 nanoparticles uniformly dispersed on ultrathin MoS 2 nanosheet arrays has been prepared through hydrothermal-pyrolysis process. At a current density (j) of 10 mA cm −2 , the potentials of NiCo 2 S 4 -MoS 2 for methanol oxidation reaction (MOR) and hydrogen evolution reaction (HER) are respectively 1.282 V and −36 mV with very high selectivity for formic acid. Importantly, under the same conditions, by using the n - n heterojunction as electrodes, the voltage (1.355 V) of the methanol electrolysis is 216 mV lower than that of the water electrolysis. Meanwhile, at higher j of 100 mA cm −2 , the voltage of the methanol electrolysis is only 6.8 % higher than the original after 150 h chronopotentiometry (CP) test. The outstanding performance of NiCo 2 S 4 -MoS 2 exceeds that previously reported in most literature, which is primarily attributed to the fact that the built-in electric field (BEF) derived from the Fermi level (E F ) difference between NiCo 2 S 4 and MoS 2 , accelerates the charge transfer, optimizes the electronic structure of the heterojunctions, and thus improving the electrical conductivity. Furthermore, MoS 2 nanosheet arrays with large specific surface area provide a fast charge/mass transfer channel, uniformly dispersed NiCo 2 S 4 and defect sites produce abundant active sites. And the superior hydrophilicity and aerophobicity of the heterojunction surface accelerate the reaction kinetics. Finally, density functional theory (DFT) calculations show that the formation of the heterojunction optimizes the electron density and d-band center of composites, thus enhancing H* adsorption and CH 3 OH dehydrogenation kinetics.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
WATER RESEARCH
·
2025
·
IF 12.4
Jung-Hyun Son,Wen-Long Wang,Peng-Hui Liu,Hang Su,Ju-Won Lee,Min-Yong Lee,Qian-Yuan Wu
This study investigates the enhancement of ozonation efficiency through the introduction of manganese ions (O 3 /Mn(II)) that significantly improve the degradation of ozone-persistent organic pollutants. Manganese ions accelerate hydroxyl radical generation by catalyzing ozone decomposition, thereby facilitating more effective oxidative reactions. The application of O 3 /Mn(II) to degrade N, N-Diethyl-3-toluamide (DEET) achieved a decomposition efficiency of 3.6 to 4.1 times higher than ozonation alone. The promotive effect was highly pH-dependent, with the observed rate constant ( k obs ) for O 3 /Mn(II) reaching 97.05 M −1 s −1 at pH 4, approximately 3.3 times greater than ozonation alone, and 686.93 M −1 s −1 at pH 7, around 1.7 times higher. O 3 oxidation contributed approximately 1% to the overall process, while hydroxyl radicals accounted for approximately 80%, and manganese species accounted for approximately 20%. Furthermore, the oxidation state of manganese significantly influenced the cooperative oxidation efficiency, with Mn(VII) achieving the highest k obs (680.87 M −1 s −1 ), while Mn(IV) exhibited the lowest (304.6 M −1 s −1 ). Additionally, intermediate products formed during DEET oxidation were identified using Orbitrap technology, elucidating various degradation pathways (such as decarboxylation, tri-hydration, and aromatic ring opening). These findings provide valuable insights into enhancing ozonation processes for environmental remediation.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ChemPlusChem
·
2018
·Vol. 83
·期 8
·787-796
·
IF 3.205
Xin Yin,Jie Li,Guojie Zhang,Zhenqi Zhang,Qing Ma,Jun Wang,Shumin Wang
Modifying the properties of energetic materials is important not only for gaining insight into the relationship between structures and properties but also for multiple applications. A new family of energetic compounds, polynitroimidazoles featuring trinitromethyl, nitromethyl and methyl acetate moieties at the nitrogen position of heterocyclic rings were synthesized. The high-energy oxidizers 2-nitro and 4-nitro-1-(trinitromethyl)-1H-imidazoles were obtained by nitration of 1-acetonylpolynitroimidazoles in fuming HNO 3 and concentrated H 2 SO 4 . 4,5-Dinitro-1-(nitromethyl)-1H-imidazole and 4,5-dinitro-1-(acetate methyl)-1H-imidazole were afforded by using 68 % HNO 3 and concentrated H 2 SO 4 through controllable synthesis. All the intermediates and the target compounds were confirmed by X-ray diffraction. It is noteworthy that one of the N-trinitromethyl nitroimidazole derivatives showed high density ( ρ : 1.88 g cm −3 ), attractive positive oxygen balance ( Ω : +18.3 %) and good detonation performance ( D : 9003 m s −1 ) exceeding those of ADN, while N-nitromethyl derivative behaved higher thermal stability and lower sensitivity in contrast to those of NG. N-acetate methyl derivative gave an interesting melt-castable property ( T m.p .: 86 o C, T d : 224 o C), acceptable detonation performance as well as low sensitivity towards impact and friction ( IS >40 J, FS >360 N), making it a competitive replacement for DNAN. These chemical and physical properties indicate that these novel materials show promising energetic performance towards future applications. Graphical A new family of neutral energetic derivatives based on polynitroimidazole backbones have been synthesized and fully characterized (see Figure). It is noteworthy that one of the N-trinitromethyl nitroimidazole derivatives showed high density (1.88 g cm -3 ), attractive positive oxygen balance (+18.3 %) and good detonation velocity (9003 m s −1 ) exceeding those of ADN, while N-nitromethyl derivative behaved higher thermal stability and lower sensitivity in contrast to those of NG. N-acetate methyl derivative gave an interesting melt-castable property, acceptable detonation performance as well as low sensitivity towards impact and friction, making it a competitive replacement for DNAN.
✓ 已验证
DOI
高影响因子
ACS Omega
·
2017
·
IF 0
Fang Wang,Houzhen Chen,Qixing Wu,Riguo Mei,Yang Huang,Xu Li,Zhongkuan Luo
Aprotic lithium–air batteries have recently drawn considerable attention due to their ultrahigh specific energy. However, the chemical and electrochemical instability of the electrolyte is one of the most critical issues that need to be overcome. To increase the stability and maintain a relatively high conductivity of the lithium ion, a mixed electrolyte of sulfolane (TMS) and N,N-dimethylacetamide (DMA) was evaluated and tested in an aprotic lithium–air battery. The physical and chemical characterizations showed that the mixed electrolyte exhibited a relatively low viscosity, high ionic conductivity and oxygen solubility, and good stability. In addition, it was found that lithium–air batteries with an optimized electrolyte composition (DMA/TMS = 20:80, % v/v) showed a better cycle life and lower charge overpotential as compared to those with electrolytes with a single solvent, either DMA or TMS.
✓ 已验证
DOI
DESALINATION
·
2025
·
IF 9.8
Minfu Mo,Yaling Lin,Danni Lin,Xiaojuan Ma,Yubin Hong,Lihui Chen,Dong Wang,Liulian Huang
Cellulose acetate (CA) has attracted much attention in the preparation of ultrafiltration membranes due to its green and sustainable characteristics. However, its poor performance (separation and antifouling performance, etc.) limits the application of CA-based membranes in water treatment. In this work, we prepared a cellulose acetate ultrafiltration membrane with enhanced separation performance by enhancing the dissolution process of CA. The dissolution process of CA was controlled by adjusting the ratio of mixed solvent ( N , N -dimethylacetamide (DMAC) and N -methyl pyrrolidone (NMP)), which could tune the phase conversion rate, optimizing the pore structures of the membranes. Compared to the single solvent (M0, M8), the optimal membrane (M4) exhibited a finger-like pore structure and the lowest surface roughness, which was favorable for achieving high water flux. As a result, the M4 possessed a comparable pure water flux (335.8 L·m −2 h −1 ) which was higher than M0 (1.8 times) and M8 (1.7 times), while the BSA rejection rate reached 96.4 %. Besides, the M4 showed a stable separation performance in different operation pressures, BSA concentration, and long-term experiments. This work provided a new method for the preparation of cellulose acetate ultrafiltration membrane with good separation performance and anti-fouling performance and also provides a new way for water treatment.
✓ 已验证
产品关联
DOI
高影响因子
DALTON TRANSACTIONS
·
2021
·Vol. 50
·期 29
·10206-10213
·
IF 4.39
Wenyao Zhang,Wenqi Jin,Meng Cheng,Ruonan Zhang,Zhihua Yang,Shilie Pan
Fluorine-containing compounds significantly enrich the diversity of inorganic chemical structures. Here, four alkaline-earth metal difluorophosphates with different space groups, namely NH4Mg(PO2F2)3 (Cmcm) (1), NH4Sr(PO2F2)3 (P) (2), (NH4)2Ba(PO2F2)4 (P2/n) (3) and Ba(PO2F2)2 (I2d) (4), were synthesized and their structures were determined for the first time. 4 is not only the first alkaline-earth-metal difluorophosphate, but also the first difluorophosphate reported to crystallize in the non-centrosymmetric space group I2d of the tetragonal crystal system. All of the three-dimensional (3D) structures of the title compounds consist of isolated (PO2F2)−, AE–O and NH4+ units, while the differences of the cation radius result in various arrangements of the (PO2F2)− units, which leads to diverse crystal structures and the disparate optical anisotropy of the crystals. According to the deep-ultraviolet (DUV) transmittance spectrum, 3 exhibits a short DUV cut off edge (<180 nm). Solid state 19F and 31P magic-angle spinning NMR spectroscopy was used to verify the presence of covalent P–F bonds in 3. The different size effects, as well as the coordination environments of the Mg2+, Sr2+, and Ba2+ cations, on the structures as a whole have been discussed in detail. In addition, the calculated birefringence values were observed to differ from 0.011 to 0.033 for the four compounds.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2026
·
IF 8.7
Meiwen Zhang,Yuqian Guo,Leilei Hou,Yun Cheng,Linghua Chen,Mengnan Cao,Hongjie Zhang
Efficient dissolution of cellulose is a critical initial stage in converting it into high value materials. In this study, we developed a rapid pretreatment method based on microwave-assisted deep eutectic solvent (MW-DES) technology to markedly reduce the dissolution time of dissolving pulp fibers in N -methylmorpholine-N-oxide (NMMO). Specifically, treatment with a ZnCl 2 /H₃PO₄ system under microwave irradiation at 200 W for 4 min effectively disrupted the hydrogen-bond network of cellulose. This treatment increased the specific surface area by 124% and reduced cellulose crystallinity from 64.06% to 44.63%. Owing to the synergistic pretreatment, the complete dissolution time in NMMO decreased to 12 min, a 60% reduction compared to the 30 min required following microwave-water (MW-water) pretreatment, and demonstrated a significant enhancement in dissolution efficiency. This approach provides a novel, sustainable strategy for the efficient pretreatment of dissolving pulp, thereby supporting the industrial production of Lyocell fibers.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2022
·Vol. 47
·期 47
·20561-20571
·
IF 7.139
Tianyu Ai,Jing Li,Shuai Nie,Yansheng Yin,Jinlin Lu,Shuo Bao,Ling Yan
Transition elements doping metal oxide is of great significance for developing gas sensors with high performance. To achieve this goal, α-Fe 2 O 3 rod and Mn-doped α-Fe 2 O 3 polyhedrons are successfully synthesized by a facile N, N-dimethylformamide assisted hydrothermal method and characterized by several physical techniques. The morphology of α-Fe 2 O 3 is evolved by introducing Mn elements. The performance of the α-Fe 2 O 3 rod and Mn-doped α-Fe 2 O 3 polyhedrons as H 2 gas sensors are studied and compared. The Mn/α-Fe 2 O 3 -5 polyhedrons sensor exhibit the best performance at optimum operating temperature of 300 °C. The response and recovery times are 10 s/24 s for H 2 with a concentration of 200 ppm, which is much faster in contrast to those recently reported H 2 gas sensors. Furthermore, α-Fe 2 O 3 rod and Mn-doped α-Fe 2 O 3 polyhedrons show abnormal n-p transition sensing behavior with the change of operating temperature. This work provides a facile method for synthesizing α-Fe 2 O 3 based sensing materials for various sensors applications.
✓ 已验证
DOI
高影响因子
RSC Advances
·
2015
·Vol. 5
·期 26
·19859-19864
·
IF 3.84
Junjun Li,Lin Zhang,Jin Gu,Yuping Sun,Xiaosheng Ji
To retain the hydroxyl group of poly(vinyl alcohol) (PVA), ammonium persulfate (APS) was used to initiate the polymerization of hydrogen on the PVA chain. Rather than hydroxyl-based cross-linking, the generated PVA macromolecule radicals were cross-linked with N,N′-methylene bisacrylamide (MBA) to prepare PVA membranes. The PVA membranes were shown to be successfully cross-linked via FT-IR characterization, as well as measurements of swelling degree and gel fraction. With increasing the content of cross-linker, the swelling degree of the membranes decreased, and the gel fraction increased. The pervaporation performance of the membrane was investigated by separating 95 wt% ethanol aqueous solutions. The cross-linked PVA membrane containing 0.5 wt% cross-linker yielded a high permeate water content (99 wt%) and a total flux of 353 g m−2 h−1 at 40 °C. As the feed temperature increased, the total flux increased, while the permeate water content decreased. The cross-linked membrane exhibited good durability over long-term operation.
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2026
·
IF 12.5
Jiangtao Meng,Tao Wang,Lei Ren,Jing Wang,Yuanyuan Zhang,Jingkuan Li,Fei Wang
Stage-matched framework reveals fuel-N pathway shifts. • Microwave shifts NH 3 and HCN release to lower temperature regions. • Microwave enriches amines and nitrile precursors in tar at lower temperatures. • Microwave promotes early char deoxygenation and condensation. • Polar O/N activation couples char-N reconstruction with tar-N evolution. Microwave-assisted pyrolysis shows promise for the clean conversion of N-rich biomass, yet its mechanism for regulating nitrogen migration remains unclear. Deashed sewage sludge and protein-derived amino acid models were employed to contrast microwave and conventional pyrolysis. This comparison utilized a reaction-stage-referenced framework based on the characteristic release regions of N-containing gases. Microwave heating did not change the basic nitrogen release pattern, with NH 3 as the dominant product and HCN as the secondary product, but substantially altered the temperature-dependent progression of the fuel-N conversion pathway. Under the present microwave experimental configuration, substantial fuel-N conversion was observed within the measured 190–300 °C range, occurring at lower measured temperatures than under conventional pyrolysis and accompanied by marked changes in O/N-containing structures. Amine intermediates were enriched in tar, and the tar-N fraction increased from about 44% to 87%, driving NH 3 release to lower temperatures. At 300–500 °C, these intermediates further underwent dehydrogenation, cyclization, and nitrilation under microwave effects, forming nitriles and low-carbon mono‑nitrogen compounds and enhancing HCN release around 300 °C. As a result, the characteristic NH 3 and HCN release regions were recorded at lower measured temperatures in the microwave system than in the conventional system. Meanwhile, microwave heating promoted early char deoxygenation and condensation, as reflected by protein-N conversion to pyrrolic-N, pyridinic-N, and nitrile-N, removal of C O and O-C=O groups, reduced interlayer spacing, and enhanced microcrystalline stacking. Tar evolved from heterocyclic and long-chain N-containing compounds toward light aromatics, oxygenated species, and low-carbon nitriles. A three-phase network is proposed wherein tar acts as an intermediate pool connecting char-N reconstruction with NH 3 /HCN release. This study provides mechanistic insights into fuel-N migration during microwave and conventional pyrolysis of N-rich sewage sludge. Download: Download high-res image (180KB) Download: Download full-size image
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）