JOURNAL OF POWER SOURCES
·
2025
·
IF 7.9
Changqing Liu,Yufei Chen,Tao Wang,Ying Wang,Conghui Liu,Xingang Kong,Jianfeng Huang,Ling Guo,Lixiong Yin
To tackle the pressing dual challenges of the energy crisis and environmental pollution , it is urgent to develop low-cost, high-activity photocatalysts for solar-driven hydrogen production. In this work, a Zn x Cd 1-x S/protonated g-C 3 N 4 S-scheme heterojunction photocatalyst is successfully constructed using an electrostatic interaction-driven assembly strategy. The optimized composite photocatalyst exhibits a hydrogen evolution rate of 17.64 mmol g −1 h −1 , which is approximately 4.14 times and 28.45 times higher than that of pure Zn x Cd 1-x S and protonated g-C 3 N 4 . The apparent quantum efficiency (AQE) of ZCSCN-20 reaches 12.3 % at 420 nm. The electrostatic interaction drives the assembly of the heterojunction, leading to an intimate interfacial contact. This close connection, in turn, significantly shortens the migration distance and transfer time of photogenerated charges. The established S-scheme charge transfer pathway enables the efficient separation of photogenerated charge carriers while preserving the strong redox capability inherent in the constituent semiconductors. Furthermore, the use of sacrificial agents to deplete photogenerated holes further suppresses charge carrier recombination, synergistically enhancing the overall catalytic activity. This work provides an efficient strategy for preparing and optimizing sulfide-based S-scheme heterojunction photocatalysts, laying a foundation for developing stable, high-performance solar-driven hydrogen production systems.
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DOI
高影响因子
ACS Applied Materials & Interfaces
·
2019
·
IF 8.456
Mingshan Wang,Hao Xu,Zhenliang Yang,Hua Yang,Anmin Peng,Jun Zhang,Junchen Chen,Yun Huang,Xing Li,Guozhong Cao
Layered tin monosulfide (SnS) is a promising anode material for sodium-ion batteries because of its high theoretical capacity of 1020 mA h g–1. Its large interlayer spacing permits fast sodium-ion transport, making it a viable candidate for sodium-ion capacitors (SICs). In this work, we designed and synthesized oriented SnS nanosheets confined in graphene in the presence of poly(diallyl dimethyl ammonium chloride) by electrostatic self-assembly during hydrothermal growth. SnS nanosheets growing along (l00) and (0l0) directions are suppressed because of the confinement by graphene, which exhibit smaller thickness and particle size. These nanostructures expose abundant open edges because of the presence of Sn4+–O, which offers rich active sites and Na+ easy transport pathways. Vacancies formed at these edges along with S and N codopants in the graphitic structure synergistically promoted Na+ surface adsorption/desorption. Such nanocomposites with SnS nanosheets confined by N,S codoped graphene demonstrated significantly enhanced pseudocapacitance. The SICs delivered excellent energy densities of 113 and 54 W h kg–1 at power densities of 101 and 11 100 W kg–1, respectively, with 76% capacity retention after 2000 cycles at 1 A g–1.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2018
·
IF 3.779
Yongkun Liu,Qiuling Lu,Zheng Huang,Shiqing Sun,Bo Yu,Uwamahoro Evariste,Guohua Jiang,Juming Yao
In this work, a novel flexible electrode material for supercapacitor is prepared by electrodeposition of Ni-Co-S interconnected nanosheet arrays on N-doped hierarchical porous carbon nanofibers (Ni-Co-S@N-pCNFs). The electrode exhibits a remarkable specific capacitance of 520.2 F g -1 at the current density of 0.2 A g −1 and 670 F g -1 at 2 mV s −1 . The activated charcoal (AC) loaded N-doped porous carbon nanofibers (AC@N-pCNFs) as electrode is also prepared which exhibits a specific capacitance of 257.2 F g -1 at 0.2 A g −1 , as well as excellent cycling stability with a capacitance retention of 92.6% after 5000 cycles. Furthermore, the Ni-Co-S@N-pCNFs as the positive electrode , active carbon loaded N-doped hierarchical porous carbon nanofibers (AC@N-pCNFs) as negative electrode , and KOH/NKK hybrids as both the electrolyte and separator are assembled into flexible asymmetric supercapacitor . The assembled supercapacitor device without using any current collectors or binders shows a high energy density of 21.6 Wh·kg −1 at a power density of 134.9 W kg −1 and robust long-term cycling stability retaining over 90.0% after 3000 cycles at 1.0 A g −1 . The as-assembled asymmetric supercapacitors (ASCs) have an outstanding mechanical flexibility and electrochemical stability and no significant attenuation occurred during cycling under different bending states.
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Ruiqi Zhang,Xintong Yao,Xinru Meng,Xinyu Li,Dafeng Zhang,Junchang Liu,Peiqing Cai,Xipeng Pu
To effectively harness solar energy, the rational construction and development of full-spectrum photocatalysts has become an appealing challenge. In this study, a novel full-spectrum responsive FeS 2 /Mn 0.3 Cd 0.7 S (FS/MCS) S-scheme photocatalyst was obtained by attaching FeS 2 nanoparticles with excellent photothermal properties on Mn 0.3 Cd 0.7 S nanorods. The photocatalytic hydrogen production rate of the optimal FS/MCS composite was 52.017 mmol·g −1 ·h −1 under full-spectrum irradiation, which was 3.88 times that of pure MCS. Based on the experimental results and density functional theory (DFT) calculations, the enhanced photoactivity of FS/MCS was attributed to the synergetic effects of photothermal and S-scheme heterojunction. The photothermal effect of FeS 2 could convert the near infrared light to heat, which elevated the local temperature of photocatalyst particles, thereby promoting the photocatalytic reaction. Meanwhile, the S-scheme heterojunction between FeS 2 and Mn 0.3 Cd 0.7 S accelerated the charge transfer and suppressed the recombination of electron-hole pairs, thereby enabling efficient charge separation while maintaining high redox potentials. This work offers a novel perspective on constructing a full-spectrum-driven photothermal-assisted photocatalytic H 2 evolution system though the dual effects of photothermal and heterojunction.
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高影响因子
CHINESE JOURNAL OF POLYMER SCIENCE
·
2016
·Vol. 34
·期 8
·981-990
·
IF 1.811
Wang Jing,Wu Ying,Liu Zheng-ping
A benign approach for efficient preparation of poly(ether sulfone) (PES) ( η
inh = 0.10−0.31 dL⋅g −1 ) has been presented by using ionic liquid (IL)/zwitterion (ZI) as reaction medium. It has been found that the interaction between 4,4′-dihydroxydiphenylsulfone (Bisphenol-S) and ZI at elevated temperatures results in efficient reduction of dehydration time, which is confirmed by TGA curves, melting point of the mixture and FTIR spectra. Furthermore, no agglomeration is observed at dehydration stage, which is attributed to the high solubility of Bisphenol-S dipotassium salt in IL/ZI. This also makes the polymerization temperature (150 °C) much lower than a conventional method (220−300 °C). In order to demonstrate the efficiency of IL/ZI as reaction medium, the polymerization was also performed in sulfolane under the same reaction condition as that in IL/ZI.
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高影响因子
CHINESE CHEMICAL LETTERS
·
2021
·Vol. 33
·期 6
·3272-3276
·
IF 6.779
Na Li,Guangmeng Qu,Xixi Zhang,Shunshun Zhao,Chenggang Wang,Gang Zhao,Peiyu Hou,Xijin Xu
The selection and development of cathode of alkaline zinc batteries (AZBs) is still hindered and often leads to poor rate capability and short cycle life. Here, amorphous hollow nickel-cobalt-based sulfides nanocages with nanosheet arrays (AM-NCS) are designed and constructed with ZIF-67 as the self-template to exchange with Ni 2+ and S 2− by using a two-step ion exchange method. The synthesized AM-NCS possess the high specific capacity (160 mAh/g at 2 A/g), and the assembled battery has excellent rate performance (146 mAh/g reversible capacity at 5 A/g). The assembled device has excellent rate performance (155 mAh/g at 2 A/g) and long cycling stability (7000 cycles, 62.5% of initial capacity). The excellent electrochemical properties of the electrode materials are mainly attributed to the unique structure, in particular, polyhedron structure with hollow structure can improve the cyclic stability, and the amorphous structure can expose more reactive sites on the surfaces of nickel, cobalt and sulfur. This work provides a new strategy for the design and fabrication of high performance cathode materials for AZBs.
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高影响因子
TRIBOLOGY TRANSACTIONS
·
2009
·
IF 0.578
Wu Hua,Li Jing,Ma Haibing,Ren Tianhui,M. Kasrai,G. M. Bancroft
The antiwear properties of three S-containing triazine derivatives with different active groups, referred to as HOT, HOMA, and TOMA, as additives in rapeseed oil (RSO) were evaluated using a four-ball friction and wear tester. The morphologies of the worn surfaces of the steel balls were observed using a scanning electron microscope (SEM). The tribochemical action mechanisms of the S-containing triazine derivatives in rapeseed oil were investigated by means of X-ray photoelectron spectroscopy (XPS) and X-ray absorption near edge structure spectroscopy (XANES). It was found that all three S-containing triazine compounds added in the rapeseed oil at a proper concentration showed rather good antiwear behavior. XPS and XANES analytical results showed that the tribofilms from the worn surfaces of the steel balls lubricated with RSO-1.2 wt% HOMA and the discs lubricated with RSO-3.0 wt% HOMA were mainly composed of some adsorbed N-, O-, and S-containing organic compounds, along with appreciable oxidized S products such as sulphite and sulphate. In contrast, the films from RSO-1.2 wt% TOMA showed a large concentration of FeS and FeS2, with a smaller amount of oxidized S products. The large difference in the chemical compositions of the tribofilms of RSO-HOMA and RSO-TOMA could be closely related to the differences in their active element content and bond types.
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高影响因子
OPTICAL MATERIALS
·
2019
·
IF 2.687
Yanling Wang,Yachao Du,Lingli Meng,Yueshu Li,Zhi Li,Qingwen Tian
Kesterite Cu 2 ZnSn(S,Se) 4 (CZTSSe) has attracted much attention as an ideal absorber material for thin film solar cells. Solution deposition methods provide a crucial approach for lowering the fabricating price of CZTSSe based photovoltaic devices . Here, a low-cost and robust ethanol/thioglycolic acid/1-butylamine ternary solutions method was developed to fabricate the CZTSSe solar cells. Characterization was performed using XRD , Raman, and C–V, which showed that the material fabricated by this method expressed high-phase purity, suitable carrier concentration, and large depletion width, and those features are vital to high efficiency photovoltaic devices . Hence, based on this high quality CZTSSe absorbed layer, photovoltaic device with a power conversion efficiency (PCE) as high as 9.71% was achieved. The PCE can be further enhanced through passivating with alkali metal and optimizing the device fabrication conditions, making this method much promising for lowering the manufacturing cost of kesterite solar cells. Additionally, this approach is full of application prospect for other burgeoning photovoltaic absorber materials which could dramatically reduce the cost of solar electricity.
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高影响因子
APPLIED ORGANOMETALLIC CHEMISTRY
·
2025
·Vol. 39
·期 11
·e70420
·
IF 0
Hui Bai,Guyu Zhang,Fengqin Tang,Lili Huang,Mingxia Tian,Libing Hu,Zhenghang Qi,Jianhui Jiang
Developing porous-structured organic semiconductor photocatalysts with high charge transfer efficiency is crucial for solar energy utilization, yet remains challenging in pollutant remediation. Herein, an S-scheme C-ZnO/B-g-C 3 N 4 photocatalyst with oxygen vacancies was fabricated through modified biomass-derived C doping for methylene blue (MB) degradation. The optimized catalyst achieved 97.8% degradation efficiency within 70 min under visible light. UV-DRS analysis revealed that C doping narrowed the bandgap and enhanced visible-light absorption. XPS results confirmed the S-scheme charge transfer pathway in C-ZnO/B-g-C 3 N 4 . The synergistic effects of C doping and oxygen vacancies significantly improved charge separation and facilitated S-scheme heterojunction formation. The catalyst exhibited superior photocatalytic performance in alkaline conditions and maintained excellent recyclability. Radical trapping experiments identified the primary reactive species as h + > ·O 2 − > ·OH in descending order of contribution. This work provides a promising strategy for solar-driven pollutant remediation by combining biomass-derived carbon modification with S-scheme heterojunction engineering.
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DOI
AICHE JOURNAL
·
2025
·
IF 4
Hai Zhang,Yixuan Meng,Fan Wang,Ze Zhang,Zhenyu Yang
This work introduces nickel (II) tetraphenylporphyrin (NiTPP) as a multifunctional electrolyte additive to simultaneously address polysulfide shuttle and uncontrolled lithium dendrite growth in lithium–sulfur (Li–S) batteries. Mobile NiTPP species act as homogeneous catalysts with Ni–N 4 centers for rapid polysulfide redox mediation to suppress migration, while planar molecules featuring lithium-affinity capability migrate to the lithium metal surfaces, enabling uniform lithium flux and anode protection. NiTPP-modified electrolytes significantly enhance Li–S battery performance, demonstrated by 634.9 mAh g −1 at 4C, 758.3 mAh g −1 after 100 cycles at 0.2 C (83.4% retention), and 757.5 mAh g −1 under high sulfur loading (2.9 mg cm −2 ) with lean electrolyte ( E / S = 5 μL mg −1 ), all with high Coulombic efficiency. Crucially, NiTPP, acting as a soluble dual-functional mediator enabling homogeneous operation in electrolytes, simplifies Li–S battery fabrication while demonstrating the commercial viability of molecularly engineered mobile active sites for stabilizing both electrodes in high-energy-density Li–S batteries.
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DOI
高影响因子
CARBON
·
2026
·
IF 12.7
Xiao Zhang,Yuan Zhuang,Haozhong Yuan,Kaixuan Wei,Renlong Ma,Huiting Hu,Zhixiang Zeng,Yuanxian Gao,Wenliang Bi,Hongchen Liu,Jian Liu
The electrocatalytic CO 2 reduction reaction (ECR) represents a promising strategy for converting CO 2 into value-added chemicals while mitigating greenhouse gas emissions. However, developing efficient and stable electrocatalysts remains challenging. In this study, we synthesized a Ni-based single-atom catalyst (Ni/NSP-C) via pyrolysis of a PZS/Ni-ZIF-8 precursor derived from ZIF-8. The resulting catalyst exhibits a hollow polyhedral structure with high surface area and porosity. Crucially, heteroatoms S and P were successfully incorporated into the primary coordination shell of Ni active sites, forming Ni-S and Ni-P bonds that modulate the electronic structure. Electrochemical tests revealed that Ni/NSP-C exhibits efficient ECR performance: a high current density of 402.3 mA cm -2 at -1.5 V vs. RHE, and CO Faradaic efficiency above 94 % over a wide potential window (-0.4 to -1.2 V), reaching 99.61 % at -0.8 V. The catalyst also demonstrated excellent stability over 24 h. Density functional theory (DFT) calculations further revealed that the S and P co-doping lowers the energy barrier for *COOH formation and suppresses the hydrogen evolution reaction, thereby enhancing ECR selectivity and efficiency. This work provides a universal coordination engineering strategy for optimizing the performance of single-atom catalysts in various electrocatalytic applications.
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DOI
高影响因子
BIOORGANIC CHEMISTRY
·
2026
·
IF 5.1
Xue Zhang,Peng Hou,Qi Zhang,Haijun Wang,Hongxia Cui,Likun Liu,Pengfei Qi,Haoqing Ren,Huiling Hou,Song Chen
Hydrogen sulfide (H 2 S) is a gas with dual roles in both environmental and biological systems. Although it is a natural atmospheric constituent and an enzymatically produced signaling molecule, elevated levels of H 2 S are associated with air pollution, cytotoxicity, and various diseases. Current methods for detecting H₂S are often limited by complex sample preparation, low sensitivity, and inadequate selectivity. To address these challenges, we report the development of a novel dual-channel and dual-responsive fluorescent probe HAR-H₂S , which enables rapid, sensitive, and selective detection of H₂S in both environmental and biological contexts. This probe employs coumarin and naphthalimide derivatives as fluorescent reporters and incorporates dual recognition sites for specific H₂S detection. Upon interaction with H₂S, the probe generates distinct blue and green fluorescent signals, facilitating bicolor imaging. The probe demonstrated excellent selectivity, low detection limits (26.4 nM and 35.1 nM), a relatively large spectral separation (126 nm) and rapid response times (within 3 min). HAR-H 2 S was successfully applied to quantify H 2 S in water samples (tap, river, and lake water) and to image H 2 S in various biological systems, including HeLa cells, HepG2 cells, zebrafish embryos, the ferroptosis model and mouse liver tissue sections. Our results highlight the potential of HAR-H 2 S as a versatile tool for H 2 S detection and imaging in both analytical and biological applications, thereby advancing the field of H 2 S research.
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DOI
PubMed
高影响因子
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