JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Li-Jie He,Jia Liu,Ting-Ting Lv,Ao-Cheng Wei,Tong-Qi Yuan
The practical applications of lithium-sulfur (Li-S) batteries have severely been hindered by notorious shuttle effect and sluggish redox kinetics of lithium polysulfide intermediates (LiPSs), which bring about rapid capacity degradation, low coulombic efficiency and poor cycling stability. In this work, 1T-rich MoS 2 nanosheets are in-situ developed onto the conductive porous carbon matrix (1T-rich MoS 2 @PC) as efficient polysulfide promotors for high-performance Li-S batteries. The porous carbon skeleton tightly anchors MoS 2 nanosheets to prevent their reaggregation and ensures accessible electrical channels, and at the same time provides a favorable confined space that promotes the generation of 1T-rich MoS 2 structure. More importantly, the uniformly distributed metallic 1T-rich MoS 2 nanosheets not only affords rich sulfphilic sites and high binding energy for immobilizing LiPSs, but also favors rapid electron transfer and LiPSs conversation kinetics, substantially regulating sulfur chemistry in working cells. Consequently, the Li-S cell assembled with 1T-rich MoS 2 @PC modified separator delivers a remarkable cycling stability with ultralow capacity decay rate of 0.067% over 500 cycles at 1C. Encouragingly, under harsh conditions (high sulfur loading of 4.78 mg cm −2 and low E/S ratio of 8 μL mg −1 ), a favorable electrochemical performance can still be demonstrated. This study highlights the profitable design of 1T-rich MoS 2 /carbon based electrocatalyst for suppressing shuttle effect and promoting catalytic conversation of LiPSs, and has the potential to be applied to in other energy storage systems.
研究领域:
材料科学
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电化学
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能源存储
✓ 已验证
DOI
高影响因子
ChemSusChem
·
2018
·Vol. 11
·期 23
·4060-4070
·
IF 7.411
Huimin Zhou,Xin Xia,Pengfei Lv,Jin Zhang,Xuebin Hou,Min Zhao,Kelong Ao,Di Wang,Keyu Lu,Hui Qiao,Malgorzata Zimniewska,Qufu Wei
Graphical Better anode by design : A designed anode structure combining the metallic conductivity of 1T-MoS 2 with interconnected TiO 2 /MoO 3 grains is beneficial for fast charge-transfer reactions and reduced transmission losses. Moreover, a flexible carbon framework buffers swollen lithium compounds, such as Li x MoO 3 and Li x MoS 2 , and supports the shrinking delithiated products, with potential for achieving high capacity stability in both Li- and Na-ion batteries. Integrating layered nanostructured MoS 2 with a structurally stable TiO 2 backbone to construct reciprocal MoS 2 /TiO 2 -based nanocomposites is an effective strategy. C@TiO 2 /MoO 3 composite nanofibers doped with 1T-phase MoS 2 nanograins were fabricated by partially sulfurizing MoO x /TiO 2 precursors. By controlling a suitable preoxidation temperature before severe thermolysis of polyvinylpyrrolidone (PVP), the MoO x /TiO 2 precursors formed a polymer-embedded array through coordination of the Mo source and pyrrolidyl groups of PVP. Sulfidation under water/solvent hydrothermal conditions led to partial formation of metallic 1T-phase MoS 2 from the MoO x precursor with preoxidation at 200 °C. After carbonization, the TiO 2 /MoO 3 /MoS 2 nanograins were encapsulated in a carbon backbone in a vertical pattern, providing both chemical contact for confined electron transport and sufficient space to adapt to volume changes. The obtained carbon-based platform not only has the advantages of an integral structure, but also exhibited ultrastable specific capacities of 540 and 251 mAh g −1 for Li-ion batteries and Na-ion batteries, respectively, after 100 cycles.
研究领域:
材料科学
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电化学
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纳米技术
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能源存储
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Yang Yang,Wenchao Hu,Fangfang Liu,Aijun Li,Dubin Huang,Ruqiang Zou
Molybdenum disulfide (MoS 2 ) has emerged as a promising anode material for lithium-ion and sodium-ion batteries, yet its practical application is limited by sluggish ion diffusion and low electrical conductivity. Herein, we propose a glucose-assisted hydrothermal strategy that simultaneously enables 1T/2H phase engineering, carbon intercalation, and hierarchical MoS 2 –carbon coupling—forming a “three-in-one” composite structure. The synthesis is achieved using halloysite-derived carbon nanotubes as templates, leading to a 1T/2H-MoS 2 /carbon composite with expanded interlayer spacing and a porous framework. As an anode material, 1T/2H-MoS 2 /C3 delivers outstanding performance, achieving 926.7 mAh g −1 after 100 cycles at 0.2 A g −1 and 544.6 mAh g −1 after 10,000 cycles at 5 A g −1 in lithium-ion cells. In sodium-ion cells, it maintains 403.4 mAh g −1 after 200 cycles at 0.2 A g −1 and 173.5 mAh g −1 after 10,000 cycles at 5 A g −1 . These remarkable enhancements arise from the synergistic effects of the “three-in-one” design, which collectively optimize electronic conductivity, lower ion diffusion barriers, and ensure structural integrity over long-term cycling.
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产品关联
DOI
高影响因子
LANGMUIR
·
2025
·
IF 3.9
Zhenyu Wen,Wenjie Zhu,Yongxue Chen,Huanhuan Sun,Lin Zhu,Yuling Yang,Yanping Song,Lei Chen,Jiajun Dong,Bingbing Liu
Surface-enhanced Raman spectroscopy (SERS) holds immense promise for molecular detection, yet the quest for high-performance, plasmon-free substrates remains active. This work pioneers the rational design and engineering of phase-tunable MoS2 nanoclusters─metallic (1T), semiconductor (2H), and, critically, hybrid metal/semiconductor (1T/2H) phases as a novel class of SERS platforms. We demonstrate this exceptional capability for ultrasensitive detection of environmentally hazardous dyes (e.g., rhodamine B, crystal violet, and methylene blue). Remarkably, the optimized 1T/2H-MoS2 substrate achieves an enhancement factor of 1.02 × 109, which ranks among the higher values for SERS substrates derived from semiconductors. Crucially, time-resolved transient photoluminescence decay spectroscopy reveals a dramatic 52% decrease in average exciton lifetime (from 3.88 to 1.86 ns) for RhB adsorbed on 1T/2H-MoS2 substrates. This profound decrease provides direct evidence for highly efficient interfacial charge transfer, predominantly driven by the built-in electric field unique to the engineered phase junction. Furthermore, by leveraging the distinct Raman signatures enabled by this heterophase substrate, we achieve the multiplex detection of all five environmental nucleobases (adenine, guanine, cytosine, thymine, and uracil) in both individual and mixed solutions. This work not only delivers fundamental mechanistic insights into charge transfer-mediated SERS but also provides a practical platform with broad implications for environmental monitoring, biomedical diagnostics, and analytical chemistry.
研究领域:
分析化学
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环境科学
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纳米技术
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光谱学
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材料科学
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生物医学诊断
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产品关联
DOI
PubMed
高影响因子
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2024
·
IF 11.2
Haonan Zhai,Huibin Liu,Yufen Zhang,Jinjin Wen,Wenyue Yang,Huiting Xu,Xiaoteng Yan,Wenchao Peng,Jiapeng Liu
Aqueous zinc ion batteries (AZIBs) are now gaining widespread attention because of their cost-effectiveness, intrinsic safety, and high theoretical capacity. Nevertheless, it is still crucial to exploit high-performance electrode materials. Herein, the freestanding 1T MoS 2 @Mxene hybrid films (MMHF) were synthesized and directly served as the cathode of AZIBs. The freestanding MMHF exhibited the hierarchical layer structure with excellent conductivity and strong interfacial interaction, which promoted the exposure of more active sites and the transfer of electrons/ions. Consequently, the MMHF displayed a high specific capacity of 270 mAh g –1 (at 0.1 A g –1 ) and good rate performance. Impressively, even after 2500 cycles under 10 A g –1 , the freestanding MMHF cathode contributed a superior specific capacity of 108 mAh g –1 with an outstanding capacity retention rate of 94.7 %. Meanwhile, the energy storage mechanism of the MMHF electrode was also elucidated through ex-situ characterizations. Furthermore, the density functional theory (DFT) computations revealed the strong interfacial interactions between 1T MoS 2 and MXene, high conductivity, and low Zn 2+ diffusion barrier. This work provides a new viewpoint for designing freestanding transition metal disulfides (TMDs) -MXene hybrid film electrodes for AZIBs.
研究领域:
材料科学
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电化学
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能源存储
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
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2022
·
IF 9.136
Zenglong Wu,Wenkai Song,Xiangwei Xu,Jiangnan Yuan,Weiyang Lv,Yuyuan Yao
Applicating co-catalyst into Fenton-like advanced oxidation processes to improve the performance for wastewater remediation has attracted widespread attention. Among them, developing highly active and green heterogeneous catalyst integrating homogeneous ferrous ions and inorganic co-catalyst is a great challenge. Herein, ascorbic acid additive was creatively introduced into the precursor composed of thiourea, sodium molybdate and ferric chloride to synthesize carbon intercalated molybdenum disulfide anchoring iron (C-MoS 2 @Fe) by a simple one-step hydrothermal method. C-MoS 2 @Fe exhibited an amazing apparent first-order constant as high as 0.739 min −1 about 10 times higher than that of the homogeneous Fe 2+ /MoS 2 system for the sulfamethoxazole (SMX) removal and achieved 68.7% removal of TOC in 6 min, which was attribute to the synergistic enhancement of high 1T phase (82.0%) and sulfur vacancies induced by the introduction of ascorbic acid. Notably, the C-MoS 2 @Fe was also capable of efficiently degrading multiple organic contaminants such as pharmaceuticals, phenolic compounds, and organic dyes. Compared with the homogeneous Fe 2+ /PMS system, the C-MoS 2 @Fe/PMS system expanded the effective pH range (2.0 ∼ 9.0) and the ultralow iron ions leaching (0.204 mg L -1 ) avoided the formation of iron containing sludge. The results of electron paramagnetic resonance (EPR), radical quenching and probe experiments indicated that •OH was the main active species with the contribution rate about 60.3%. Furthermore, possible degradation pathways were proposed based on the intermediate products of SMX investigated by LC-MS. This study provides novel insights for the development of highly active and green catalysts for wastewater remediation.
研究领域:
环境科学
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化学工程
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材料科学
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水处理
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产品关联
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2023
·
IF 22.1
Qing-rui Zeng,Zi-ang Jia,Xu Liu,Bo-wen Xiu,Jin-ping Cheng
The rational application of piezoelectric polarization properties in non-centrosymmetric heterojunctions to improve charge separation efficiency is a novel approach for enhancing their photoelectrocatalytic capabilities for environmental purification. Herein, a noval 1T-2H MoS 2 QDs/Y-NaBi(MoO 4 ) 2 multiple heterostructures with two types S-scheme heterojunctions was formed by multi-functional materials NaBi(MoO 4 ) 2 with Y 3+ ion-doping and multi-phase state (1T, 2H and 1T-2H) MoS 2 quantum dots multi-interface polarization engineering. Material characterization and DFT calculations revealed that 1T-2H MoS 2 QDs/Y-NaBi(MoO 4 ) 2 multiple heterostructures produce highly-efficient Bi-S-Mo(IV) and Mo(IV)-S-Mo(VI) charge-transfer channels induced by multi-interface polarization engineering. 1T-2H MoS 2 QDs/Y-NaBi(MoO 4 ) 2 heterostructures were developed as photoanodes using the pressed tablet stainless-steel mesh (PT-SSM) method, and demonstrated conspicuous piezoelectric-photoelectrocatalytic (PZ-PEC) efficiency (99.88% removal within 40 min) for the degradation of organic pollutant phosphodiesterase-5 inhibitor (PDE-5i) under visible light illumination, direct-current external bias and mechanical force. This work provides new insight for synergy and mechanism between piezoelectric effect and photoelectrocatalysis for environmental clean-up.
研究领域:
材料科学
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环境科学
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电化学
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纳米技术
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催化
✓ 已验证
产品关联
DOI
高影响因子
ChemSusChem
·
2021
·Vol. 14
·期 21
·4752-4763
·
IF 8.928
Zhiqiang Li,Wei Zhou,Yuan Tang,Xin Tan,Yizhong Zhang,Zikang Geng,Yuchen Guo,Lequan Liu,Tao Yu,Jinhua Ye
Graphical The schottky heterojunction is constructed based on the Fermi energy level difference between the metal phase 1T-WS 2 and Zn 0.5 Cd 0.5 S. Under visible light irradiation, the tight interfacial contact leads to strong electronic interactions and facilitates the transfer of photogenerated carriers from Zn 0.5 Cd 0.5 S to 1T-WS 2 , further enhancing photocatalytic hydrogen production. Due to inefficient charge separation and low surface catalytic conversion efficiencies, cocatalysts are required for achieving photocatalytic hydrogen evolution. Being a noble-metal-free cocatalyst, metallic 1T-WS 2 with excellent conductivity can function for this reaction. Herein, 1T-WS 2 /Zn 0.5 Cd 0.5 S is constructed via a simple and feasible grinding approach. The composite containing 7.5 % 1T-WS 2 in 1T-WS 2 /Zn 0.5 Cd 0.5 S achieves a hydrogen evolution rate of 61.65 mmol g −1 h −1 and an external quantum efficiency of 8.04 % at 420 nm, which is 37 times that of bare Zn 0.5 Cd 0.5 S (1.67 mmol g −1 h −1 ). The electrical conductivity of metallic 1T-WS 2 reduces the transfer impedance at the interface and thus accelerates the non-radiative energy transfer and electron transport rate. The different Fermi levels of 1T-WS 2 and Zn 0.5 Cd 0.5 S form a Schottky junction, which promotes the transfer of photogenerated electrons from Zn 0.5 Cd 0.5 S to 1T-WS 2 . More importantly, the close interface contact between 1T-WS 2 and Zn 0.5 Cd 0.5 S results in strong electron interactions, which is conducive to the spatial separation of photogenerated electrons and holes. This work will further expand the application of 1T-WS 2 in the photocatalytic hydrogen evolution process.
研究领域:
材料科学
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催化
·
光催化
·
能源材料
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ACS Nano
·
2025
·
IF 16
Yao Yao,Yue Zhao,Huijuan Zhang,Wenting Pan,Wei Liang,Yijian Jiang,Xinlong Yan,Yinzhou Yan
The development of surface-enhanced Raman spectroscopy (SERS) as an ultrasensitive fingerprint analysis technique in precision medicine requires high-performance SERS substrates with controllable nanostructure (hot-spot) distribution, simple fabrication, superior stability, biocompatibility, and extraordinary optical responses. Unfortunately, fabrication of arbitrary nanostructures with high homogeneity on a large scale for SERS is still challenging. Herein, we report an ultrafast laser parallel fabrication protocol for Au/2D-transition-metal dichalcogenide hybrid SERS biosensors. The leveraged photonic nanojets (PNJs) are generated by a micron-sized microsphere monolayer to simultaneously trigger localized phase transition in 2H-MoTe2, achieving a 1T′-MoTe2 nanopattern array with a density of 1 million per mm2 by a single laser shot. The Au nanoparticle clusters (AuNCs) are subsequently grown in situ from the 1T′ regions, creating a AuNCs on 1T′/2H-MoTe2 (AuNCs@1T’/2H-MoTe2) hybrid SERS substrate. The fabricated feature diameter and overlay accuracy of the patterned AuNCs are 210.1 ± 3.4 and 9.2 ± 1.7 nm, respectively. To eliminate background noise, we designed dimer-AuNCs@1T′/2H-MoTe2 (dAuNCs@1T′/2H-MoTe2), achieving a detection limit of 10–13 M with an enhancement factor of 4.9 × 108 for the methylene blue (MB) analyte. The strong localized surface plasmon resonances in the dAuNCs as well as efficient charge transfers between Au, 2H-MoTe2, and MB contribute to the majority of Raman enhancement. The multiscale dAuNCs@1T′/2H-MoTe2 array provides a powerful SERSome (comprising multiple SERS spectra) platform for therapeutic drug monitoring, by which we successfully identified the metabolic behaviors of living gastric adenocarcinoma cells administered with two drugs, i.e., capecitabine, oxaliplatin, and their combination. The present work establishes opportunities for creating a highly ordered nanopattern array for ultrasensitive SERSome analysis of cell metabolism in cancer therapy.
研究领域:
纳米技术
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生物医学工程
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分析化学
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癌症研究
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材料科学
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光学与光子学
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精准医学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2019
·Vol. 54
·期 20
·13247-13254
·
IF 3.442
Liu Hao,Chen Bochao,Liao Libing,Fan Peng,Hai Yun,Wu Yuanyuan,Lv Guocheng,Mei Lefu,Hao Huiying,Xing Jie,Dong Jingjing
Metallic 1T MoS 2 greatly benefits the supercapacitance of MoS 2 due to its considerably higher conductivity as compared to semiconducting 2H MoS 2 . Alkali metals, such as Li, Na and K, are always used to prepare 1T MoS 2 through intercalation of alkali metal ions into the interlayer of 2H MoS 2 . Nevertheless, the influences of the alkali-earth metals as the guest in the interlayer of MoS 2 on its structure and electrochemical capacitor performance are rarely investigated. Herein, we introduced hydrated Mg ions as the guest into MoS 2 nanosheets. The interlayer spacing was increased to 1.144 nm after the introduction of hydrated Mg ions, larger than that of the pristine MoS 2 (0.620 nm) and restacking MoS 2 (0.626 nm). The enlarged interlayer spacing can accommodate more ions during intercalation process. Moreover, the 1T phase concentration after the introduction of hydrated Mg ions was as high as ~ 90%, which benefits the charge transfer during the charging/discharging processes. Consequently, the specific capacitance of the MoS 2 with Mg guest ions as well as the energy densities and power densities was greatly improved as compared to those of the restacking MoS 2 or pristine MoS 2 counterparts. The present work not only demonstrated a new strategy for engineering the physical properties and improving the electrochemical performance of MoS 2 supercapacitor electrode through pre-intercalation of alkali-earth metal ions in the interlayer of MoS 2 , but also has directive significance for the design of other layered electrode materials for energy storage systems.
研究领域:
材料科学
·
电化学
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产品关联
DOI
高影响因子
Nano Energy
·
2022
·
IF 19.069
Sin-Yi Pang,Weng-Fu Io,Lok-Wing Wong,Jiong Zhao,Jianhua Hao
Crystal phase modulations in two-dimensional (2D) materials have garnered extensive interest because of their intriguing features and potential applications. Nonetheless, synthesizing some specific phases of metastable transition metal dichalcogenides (TMDs) remains a challenge due to the restricted selectivity under chemical and physical treatments, especially for direct growth of specific phase of TMDs on 2D substrates to form heterostructures . Taking the merits of MXene with tunable atomic vacancies and surface chemistry via surface functionalization , the phase of epitaxially grown TMDs on 2D MXene can be significantly affected. In this work, 1 T′-MoS 2 and 1 T-MoSe 2 were directly grown on electrochemically synthesized MXene under controlled oxidization conditions and selected MXene substrate. Owing to the synergistic effect of TMDs and MXene, the TMDs/MXene heterostructure catalysts exhibit good electrochemical activity under acidic conditions, with a low overpotential of 167 mV at a current density of 10 mA cm −2 . Our work not only demonstrates the distinct chemical characteristic of various MXenes feasible for surface engineering which promotes the direct and in situ growth of phase controlled TMDs on MXene substrates but also displays the high electrochemical activity in TMDs/MXene heterostructure catalysts.
研究领域:
材料科学
·
电化学
✓ 已验证
产品关联
DOI
高影响因子
ENERGY & FUELS
·
2023
·
IF 5.3
Jun Tang,Jinzhao Huang,Sixuan Zhang,Zehui Liu,Xiaolong Deng
Metal-phase MoS2 (1T-MoS2) is considered a promising candidate as a catalyst for the hydrogen evolution reaction (HER). However, the instability of 1T-MoS2 limits its electrocatalytic activity. Herein, we first synthesized 1T-MoS2 with excellent HER catalytic performance by a simple one-pot hydrothermal strategy of introducing the d-electron-rich transition metal atom Ni into MoS2. A bimetallic monatomic catalyst (Pt@1T-MoS2–Ni) was also prepared by modifying 1T-MoS2–Ni with Pt single atoms (Pt SAs). Experiments show that the electron transfer caused by Ni doping leads to the 1T phase transition, and the modification of Pt SAs further improves the electrical conductivity. These two factors synergistically modulate the electronic composition of MoS2 and increase the number of reactive sites. In consequence, the Pt@1T-MoS2–Ni catalyst exhibits significantly enhanced HER activity, achieving an overpotential as low as 76 mV at 10 mA/cm2 with the corresponding Tafel slope of only 46 mV/dec. Moreover, the current attenuation is negligible within 12 h, surpassing the performance of MoS2. This study offers ideas for improving the efficiency and stability of 1T-MoS2 catalyst designs.
研究领域:
材料科学
·
电催化
·
能源化学
✓ 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）