CHEMICAL ENGINEERING JOURNAL
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2021
·
IF 13.273
Jingdong Li,Arthur Listwan,Jianxing Liang,Feng Shi,Kan Li,Jinping Jia
In this work, defect-rich 1 T-MoS 2 nanosheets are successfully synthesized by solvothermal method with acetic acid as the templating agent. It is found that changing the concentration of acetic acid can regulate the proportion of 1 T phase and affect the activity of hydrogen evolution. Under the optimum concentration of acetic acid, the overpotential is as low as 136 mV at the current density of 10 mA cm −2 with a Tafel slope at only 45 mV dec −1 , which shows an attractive potential for the development of electrocatalytic hydrogen evolution. In addition, the addition of acetic acid prevents the agglomeration of 1 T-MoS 2 and thus increases the stability of electrode materials, which is conducive to the long-term hydrogen evolution reaction and cost control. Most importantly, according to comparing several small molecular carboxylic acids, the probable formation mechanism of 1 T-MoS 2 nanosheets is proposed.
研究领域:
材料科学
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电化学
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DOI
高影响因子
ENERGY & FUELS
·
2026
·
IF 5.3
Rong Ma,Yuxin Xie,Xudong Hu,Hao Wang,Dandan Yuan,Zhida Li,Deqiang Ji,Hongjun Wu
Metallic-phase MoS2 (1T-MoS2) is considered a promising catalyst for the hydrogen evolution reaction (HER) in acidic media, largely due to the abundant surface active sites induced by sulfur vacancies (SV). However, existing defect engineering approaches for MoS2 often involve corrosive chemicals or specialized equipment, hindering its practical scalability. In this work, 1T-MoS2 is synthesized via a facile one-step hydrothermal method, and defect engineering is achieved simply by modulating the sulfur-to-molybdenum (S/Mo) molar ratio in the precursor solution. The optimized catalyst exhibits a low HER overpotential of 266 mV at −10 mA cm–2 and a Tafel slope of 72 mV dec–1 in a 0.5 M H2SO4 electrolyte. It also shows outstanding operational stability, with only a 15 mV increase in overpotential at −10 mA cm–2 after 150 h of continuous HER testing under −0.7 V vs RHE (∼200 mA cm–2). The enhanced performance is attributed to multiple synergistic effects induced by SV defects, including reduced charge transfer resistance, accelerated reaction kinetics, and an enlarged electrochemically active surface area. Overall, this work offers a simple, scalable route to prepare SV-tuned 1T-MoS2, and it provides useful design insights for developing efficient and durable MoS2-based HER electrocatalysts.
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高影响因子
ACS Applied Nano Materials
·
2024
·
IF 5.3
Jingui Han,Zhitao Shao,Yaozu Jia,Peiyao Liu,Zuqi Han,Xitian Zhang,Lili Wu,Xinzhi Ma
The practical applications of lithium–sulfur (Li–S) batteries have been significantly impeded by the heavy shuttle effect and slow bidirectional conversion of lithium polysulfides (LiPSs). In this study, a hierarchical NiS2/1T-MoS2 nanocomposite is utilized as a functionalized separator modifier to overcome the challenges. The MoS2 nanosheets are vertically and uniformly aligned on the surface of NiS2 microspheres, constructing a hierarchical yolk–shell structure. The NiS2 support not only significantly reduces the agglomeration of MoS2 nanosheets but also effectively stabilizes their 1T-phase structure, which is highly desirable for high-performance Li–S batteries. The Li–S battery with the NiS2/MoS2–CNT-modified separator delivers an excellent initial specific capacity of 1228 mA h g–1 at 0.2 C with a high-capacity retention of 85% over 100 cycles. It even achieves a discharge capacity of 722 mA h g–1 at 5 C. Furthermore, it maintains remarkable cycling stability with only 0.051% capacity decay per cycle during the long-term cycles at 1 C. This study not only provides a viable scheme for separator modifier design toward advanced Li–S batteries but also offers a universal route for stabilizing the 1T-phase structure of MoS2.
研究领域:
材料科学
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电化学
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能源存储
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DOI
高影响因子
Nanomaterials
·
2021
·Vol. 11
·期 12
·3273
·
IF 5.076
Kunjie Wang,Jiahui Zhang,Yachen Ye,Hongbin Ma,Bingxin Liu,Peng Zhang,Benhua Xu
1T-phase molybdenum disulfide is supposed to be one of the non-precious metal-based electrocatalysts for the hydrogen evolution reaction with the highest potential. Herein, 1T-MoS2nanosheets were anchored on N-doped carbon nanotubes by a simple hydrothermal process with the assistance of urea promotion transition of the 1T phase. Based on the 1T-MoS2nanosheets anchored on the N-doped carbon nanotubes structures, 1T-MoS2nanosheets can be said to have highly exposed active sites from edges and the basal plane, and the dopant N in carbon nanotubes can promote electron transfer between N-doped carbon nanotubes and 1T-MoS2nanosheets. With the synergistic effects of this structure, the excellent 1T-MoS2/ N-doped carbon nanotubes catalyst has a small overpotential of 150 mV at 10 mA cm−2, a relatively low Tafel slope of 63 mV dec−1, and superior stability. This work proposes a new strategy to design high-performance hydrogen evolution reaction catalysts.Keywords:1T-MoS2nanosheets;N-doped carbon nanotubes;hydrogen evolution reaction;water splitting;synergy effects
研究领域:
材料科学
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电化学
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DOI
PubMed
高影响因子
RSC Advances
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2023
·Vol. 13
·期 50
·35689-35694
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IF 3.9
Huandi Hou,Ting Wang,Baohuan Wang,Wenting Guo,Xiang Miao,Xin Liang
Co–Mo–S based catalysts have promising applications in both the hydrogen evolution reaction (HER) and hydrodesulfurization (HDS). Herein, Co–Mo–S catalyst and Co–Mo–S catalyst with and without NaBH4 modification have been successfully synthesized by a simple hydrothermal synthesis method. Co–Mo–S catalysts with NaBH4 modification show better catalytic activity towards both HDS and the HER. The phase purity, morphology, crystal structures and electron valence distribution of the catalysts with and without NaBH4 modification were studied by experimental characterizations and theoretical calculations. The catalysts without NaBH4 modification are mostly 2H-MoS2, while the catalysts without NaBH4 modification have 1T-MoS2, and 1T-MoS2 is exposed to more active sites, which will be conducive to the results of HDS performance of the catalyst. DFT calculations investigated the required activation energies of 1T-MoS2 and 2H-MoS2 for HDS and HER, respectively. The activation energy required for both HDS and H2 generation of 1T-MoS2 is significantly lower than that for the 2H-MoS2 structure.
研究领域:
催化化学
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材料科学
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理论计算
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DOI
PubMed
高影响因子
Journal of Energy Chemistry
·
2026
·
IF 15.6
Zhiqiang Liu,Henghui Jin,Yongping Du,Weicheng Zhan,Leiming Lang,Guangxiang Liu,Jiangtao Yuan,Pan Feng,Li Tao,Jian Zhang,Guoqiang Luo,Changlin Dong,Jiajun Gu,Wenshu Chen
Restacked two-dimensional (2D) material thin films offer a promising approach for achieving high volumetric energy density supercapacitors, but their ultimate rate performance is constrained by electrolyte ion transport properties. This work systematically investigates the electrochemical behaviors and underlying mechanisms of restacked 1T−MoS 2 films in various aqueous electrolytes. In 1 M CsCl electrolyte, an 8.5-μm-thick 1T−MoS 2 film electrode exhibits ultrafast ion storage kinetics with a b -value of 0.94 and a remarkable volumetric capacitance ( C v ) of 221 F cm −3 at 1,000 mV s −1 , significantly outperforming other ionic systems. The electrode also demonstrates excellent cycling stability with 87% capacitance retention after 10,000 cycles at 10 A g −1 . Compared to reported advanced graphene, MXene, and oxide-based electrodes, the 1T−MoS 2 film electrodes in 1 M CsCl show an integrated advantage of ultrathin characteristic and ultrahigh C v under considerable high scan rates of 500 to 1,000 mV s −1 . Theoretical calculations reveal that Cs + possesses the lowest diffusion barrier between 1T−MoS 2 interlayers, where its weak solvation effect facilitates rapid ion storage kinetics. This work not only elucidates the ultrafast transport mechanism of Cs + within confined 2D spaces, but also provides insights into developing next-generation ultrafast energy storage devices with high volumetric energy densities through optimized electrolyte–electrode synergy. The electrochemical ion storage behaviors and underlying mechanisms of restacked 1T−MoS 2 film electrodes in various aqueous electrolytes were systematically investigated. The electrodes exhibit ultrafast charge storage kinetics in 1 M CsCl, demonstrating the combined advantages of ultrathin feature and ultrahigh volumetric capacitance at scan rates as high as 1000 mV s −1 , significantly outperforming state-of-the-art reported electrode materials. Download: Download high-res image (188KB) Download: Download full-size image
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高影响因子
ACS Applied Materials & Interfaces
·
2021
·
IF 9.229
Cheng Lin,Lianfu Jiang,Dawei Hu,Yiqun Li,Bo Cai,Jing Li,Yu Gu,Luyang Wang,Kan Zhang,Haibo Zeng
Although research progress on mimicking natural photosynthesis for solar-to-fuel conversion has been continuously made, exploring broadband spectral-responsive materials with suitable band positions and high stability still remains a huge challenge. Herein, we, for the first time, report novel AsP nanosheets (NSs) with P-type semiconducting property and enough negative conduction band, which can work as a stable near-infrared (NIR) region-responsive electron donor for water reductive hydrogen (H2) production. To mimic photosystem I, Au nanorods (NRs) act as electron transport media, which are also responsible for the enhanced electric field nearby, and 1T-MoS2 NSs as a hydrogen evolution catalyst are orderly coupled with AsP NSs with a sheet-rod-sheet structure by electrostatic self-assembly. The cascaded band level alignment enables unidirectional electron flow from AsP to Au and then to MoS2, and the optimum H2 production rate of the MoS2-Au-AsP ternary heterojunction reaches 125.52 μmol g–1 h–1 with good stability even after being stored for several months under light irradiation with a wavelength longer than 700 nm. This work provides a platform that is energetically tailored to drive a solar broad-spectrum fuel generation, including CO2 reduction and N2 fixation.
研究领域:
材料科学
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能源化学
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光催化
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产品关联
DOI
PubMed
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2023
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IF 5.2
Hankui Sang,Congming Tang,Kai Ma,Xinli Li
The scarcity of fresh water resources necessitates us to develop an efficient technique for sustainable production of clean water from seawater and wastewater. Here, we constructed the 1 T-MoS 2 /PDA (polyaniline) as a photothermal material for purification of seawater and wastewater to produce clean water through interfacial evaporation by virtue of sunlight. 1 T-MoS 2 has a higher evaporation capacity of water than 2 H-MoS 2 , which was selected to prepare 1 T-MoS 2 /PDA composite for photothermal conversion. As expected, 1 T-MoS 2 /PDA composite offers a higher evaporation rate of water than both 1 T-MoS 2 and PDA , which owes to an excellent light absorbance, low light reflectance and good wettability . Under irradiation of 1 sun, the evaporation rate of water over the 1 T-MoS 2 /PDA composite in pure water reached 1.51 kg m −2 h −1 , and the photothermal conversion efficiency reached 92%. Encouragingly, 1 T-MoS 2 /PDA composite can be well used to treat real seawater and various wastewater such as organic dye solution and heavy metal ion solution, in which the evaporation rate of water is close to pure water, and the quality of water is better than the standard of drinking water established by the World Health Organization (WHO). Besides, 1 T-MoS 2 /PDA composite still maintain an excellent evaporation performance after treatment of acidic solution and alkaline solution, indicating an excellent durability. This work provides a feasible solution for producing clean water by solar-driven interfacial evaporation from seawater and wastewater.
研究领域:
环境科学
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材料科学
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产品关联
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2025
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IF 5.4
Shan Li,Longlong Zhang,Bin Xu,Weihua Qin,Mengdan Wang,Bingli Pan,Hongyu Liu,Honggang Wang
Nanoparticles are of great significance to enhance tribological performances and can be employed as effective lubricant additives. 1T-MoS 2 has been widely applied in many fields. However, it is rarely studied in lubrication application. In this study, a novel core-shell lubricant additive was prepared by combining CuNi-MOF and 1T-MoS 2 via a facile hydrothermal method. The as-prepared CuNi-MOF@1T-MoS 2 exhibited a flower-like structure. Both experimental and theoretical calculation results showed the interlamellar interactions between the layered 1T-MoS 2 and CuNi-MOF sheets. Tribological properties of PEG200 containing CuNi-MOF@1T-MoS 2 were systematically investigated by a four-ball test machine. In comparison with PEG200, the friction coefficient and wear scar diameter were remarkably reduced by 56.8 % and 34.0 %, respectively. Therefore, the combination of 1T-MoS 2 and CuNi-MOF presents a promising candidate for enhancing the tribological properties of PEG200.
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高影响因子
Nano Futures
·
2022
·Vol. 6
·期 2
·025001
·
IF 4.07
Yu-Ting Wang,Ze-Zhi Zhang,Ming-Xue Li
Two-dimensional transition metal dichalcogenides are regarded as the ideal hosts for zinc-ions. Herein, a facile hydrothermal method is proposed to fabricate the metallic phase (1T phase) MoS2/multi-walled carbon nanotube (MWCNT) hybrids serving as the cathode materials for zinc-ion batteries (ZIBs). By virtue of the exertion of phase engineering and the synergy between the 1T MoS2 nanosheets and MWCNT framework, the transfer kinetics of zinc-ions of the prepared hybrid are remarkably accelerated, leading to boosted electrochemical properties at both room temperature and low temperatures. The hybrid electrode delivers a high reversible capacity of 161.5 mAh g−1 after 100 cycles at 0.1 A g−1, and good cycling stability with a desired capacity retention of 84.6% over 500 cycles at 1 A g−1. Furthermore, its boosted capability of zinc-ion storage in a low-temperature atmosphere is revealed. This work not only provides an effective way to squeeze the values of phase engineering of MoS2 in ZIBs, but also reveals the great potential of MoS2-based composites in low-temperature energy storage devices.
研究领域:
材料科学
·
电化学
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DOI
高影响因子
CARBON
·
2019
·
IF 7.466
Raheela Naz,Muhammad Imtiaz,Qinglei Liu,Lulu Yao,Waseem Abbas,Tengfei Li,Imran Zada,Yang Yuan,Wenshu Chen,Jiajun Gu
Highly defective molybdenum disulfide (MoS 2 ) nanosheets of 1T phase are synthesized on a three-dimensional reduced graphene oxide (3D RGO) network through a one-pot hydrothermal method . By switching the reaction time, the resulting MoS 2 's phases (1T or 2H) and defect-density are successfully controlled. Reducing the reaction time from 20 to 6 h increases the defect-density and induces a phase transition from hybrid 2H/1T to 1T phase. High defect-density coupled with high 1T-phase portion in MoS 2 nanosheets/RGO heterostructures enhances the electrochemical performance for supercapacitor application by inducing additional active sites, which provide fast charge transfer rate and a large number of ion diffusion channels. Among all samples, the defect rich 1T-phase MoS 2 nanosheets/RGO heterostructure synthesized in 6 h (M/RGO-6) gives an outstanding specific capacitance of 442.0 F g −1 at a current density of 1 A g −1 . The M/RGO-6 also exhibits excellent cycling stability with capacitance retention of 90.3% over 1000 cycles at 5 A g −1 . These make M/RGO-6 attractive to the electrode of high-performance supercapacitors .
研究领域:
材料科学
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能源存储
✓ 已验证
产品关联
DOI
高影响因子
Journal of Materials Chemistry A
·
2023
·Vol. 12
·期 5
·2760-2770
·
IF 11.9
Binchao Shi,Yue Wang,Ertai Liu,Shilin Mei,Chang-Jiang Yao
The fast capacity decay and limited cycling life are the two main issues that hinder the practical applications of lithium–sulfur batteries. They are mainly caused by the shuttle effect of polysulfide species and the growth of big lithium dendrites occurring separately on the cathode and anode sides. To simultaneously tackle these problems, we explore a multifunctional interlayer integrating the aligned nanochannel structure of an anodic aluminum oxide (AAO) membrane with porous 1T MoS2 nanotubes (namely MoS2@AAO). Benefiting from the high electronic conductivity, sulfiphilic and lithiophilic properties of 1T MoS2, and the positive surface plus low tortuosity of the straight channels of AAO, the designed interlayer not only guarantees rapid ion/electron transfer and efficacious suppression of the polysulfide shuttle, but also achieves uniform and stable lithium deposition during cycling. Consequently, the MoS2@AAO interlayer exhibits a high capacity retention of 99.6% at 0.2C after 500 cycles and 90.6% at 1.0C after 1000 cycles. The prototype cathode with a sulfur loading of 5 mg cm−2 was also investigated, which exhibited over 96% retention of the initial discharge capacity at 0.1C after 50 cycles. This work provides a new solution for simultaneously stabilizing both the lithium anode and sulfur cathode via an integrating approach.
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
危险品化学品经营许可证（带存储）