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Journal of Materials Chemistry C · 2022 ·Vol. 10 ·期 48 ·18164-18173 · IF 8.067

Hollow cubic CdS@CoS/WS2 dual S-scheme heterojunction superstructure toward optimized photothermal–photocatalytic performance

Weifeng Kong,Zipeng Xing,Hang Zhang,Bin Fang,Yongqian Cui,Zhenzi Li,Peng Chen,Wei Zhou

A hollow polyhedral structure can effectively capture light and facilitate carrier separation, thus enhancing photocatalytic performance. Herein, hollow cubic CdS@CoS/WS2 dual S-scheme heterojunction superstructure photocatalysts are fabricated using a simple sulfidation and hydrothermal method. CdS@CoS/WS2 with a band gap of 1.59 eV and a relatively narrow band gap broadens the photoreaction to the near-infrared region and shows a good photothermal effect, which can promote photocatalytic reactions. It shows a relative specific surface area of 91.58 m2 g−1, which provides abundant surface-active sites to enhance the photocatalytic reaction. Under light conditions, the photocatalytic degradation ratios of CdS@CoS/WS2 for tetracycline and bisphenol A are up to 98.9 and 99.1%, and the hydrogen evolution efficiency is also up to 10.62 mmol h−1 g−1. The enhanced photothermal–photocatalytic performance could be due to the formation of a dual S-scheme heterojunction superstructure that facilitates space charge separation, a narrow band gap and a mesoporous hollow structure promoting solar light utilization, providing abundant surface-active sites and enhanced mass transfer. This simple strategy provides a new idea for the construction of high-performance hollow superstructure photocatalysts.

研究领域: 材料科学 · 环境科学 · 化学工程
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2023 · IF 22.1

Bifunctional TiO2/COF S-scheme photocatalyst with enhanced H2O2 production and furoic acid synthesis mechanism

Yi Yang,Jingjing Liu,Miaoli Gu,Bei Cheng,Linxi Wang,Jiaguo Yu

Coupling photocatalytic H 2 O 2 evolution with simultaneous furfuryl alcohol oxidation can avoid the slow water oxidation reaction and fully utilize photogenerated carriers to produce valuable chemicals. Herein, a COF (denoted as BTTA) was synthesized by the Schiff-base condensation and in-situ grown on the surface of TiO 2 nanofibers. The resultant TiO 2 /BTTA composite has a large interface and a short carrier migration distance. Furthermore, the porous and ultrathin BTTA layers endow the composites abundant active sites and excellent light absorption ability. Remarkably, a H 2 O 2 -evolution rate of 740 μmol L −1 h −1 and a furoic alcohol conversion of 96 % are achieved. In-situ irradiated X-ray photoelectron spectroscopy and electron spin resonance confirm the S-scheme carrier transfer mechanism, which spatially separates photogenerated carriers with strong redox power. This work opens a new door to the rational design of S-scheme photocatalysts for economic and green photosynthesis of H 2 O 2 and organic compounds.

研究领域: 材料科学 · 环境科学 · 化学工程
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REACTIVE & FUNCTIONAL POLYMERS · 2023 · IF 5.1

Noninterventional target-embolization combined with NO gas therapy for solid tumors by pH-responsive poly(amino acid)s with S-nitrosothiols group

Zhengpeng Chen,Lei Wang,Yuanyuan Jin,Hongyun Guo,Yongdong Zhang,Mingzhong Ma,Xiaobo Wang,Xing Zhou,Ziqiang Lei,Dedai Lu

Gas therapy and embolization are important treatment methods for solid tumors. In order to improve the efficacy of NO therapy and simplify the operation of interventional embolization, we designed and prepared the microacidic-gelled poly[(L-Glutamic acid- ran -L-Tyrosine)- b -L-Threonine- b -L-S-nitrosocysteine]s (PGTTSNCs, obtained by the reaction of tert-butyl nitrite with thiol side groups of poly[(L-Glutamic acid- ran -L-Tyrosine)- b -L-Threonine- b -L-Cysteines]s, PGTTCs.) for noninterventional embolization combined with NO gas therapy for solid tumors. The results of in vivo experiments indicated that PGTTSNCs from PGTTCs-6.4 (the gelled-pH value is 6.4) has significant target-accumulation and therapy effects, and at 10 days post-injection only scars were found at the tumor site. After 20 days, the tumors of model mice were completely disappeared. The method is extremely simple and efficient for solid tumors, which is not only a great innovation of tumors theranostic, but also a qualitative development in nanomaterials .

研究领域: 肿瘤学 · 纳米医学 · 生物材料学
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Preparation of S-doped g-C3N4 with C vacancies using the desulfurized waste liquid extracting salt and its application for NOx removal

Liyuan Duan,Guoqiang Li,Shuting Zhang,Hongyu Wang,Yongle Zhao,Yongfa Zhang

In this study, graphitized carbon nitride photocatalysts were successfully prepared by using the desulfurized waste liquid extracting salt from coking plants. The NO x removal efficiency of g-C 3 N 4 synthesized using ammonium thiocyanate (NH 4 SCN), ammonium thiosulfate ((NH 4 ) 2 S 2 O 3 ) and ammonium sulfate ((NH 4 ) 2 SO 4 ) with different mass ratios were evaluated. The results showed that due to the addition of (NH 4 ) 2 S 2 O 3 and (NH 4 ) 2 SO 4 a large amount of sulfur-containing gas was released during pyrolysis, which significantly increased the specific surface area and pore volume of the photocatalysts. The release of sulfur-containing gas also resulted in the incorporation of sulfur, and due to this doping process the band gap of the photocatalyst was widened to 2.94 eV, thus enhancing its visible light response. C vacancies were formed in the hepazine ring, which increased the electron density around the N–(C) 3 bridge bond and formed an electron trapping center, thus inhibiting the recombination of charge carriers. The photocatalysts had increased O 2 adsorption capacity and increased number of amino groups on their surface. This facilitated the rapid generation and consumption of reactive oxygen species, inhibited the accumulation of NO 2 on the surface, reduced the production of NO 2 , thus improving the NO x removal efficiency of the photocatalysts. The principle of using “waste for waste control” was achieved, and a new method for nitrogen oxide removal was provided.

研究领域: 环境科学 · 材料科学
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PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY · 2025 · IF 4

Functional characterization of an epsilon glutathione S-transferase (SfGSTe9) associated with insecticide detoxification in Spodoptera frugiperda

Wei-Huan Xu,Meng-Yao Zhu,Zhi-Heng Xu,Xiao-Jie Li,Chao-Yang Peng,Xiao-Pei Fan,Yong-Qiang Li

The fall armyworm, Spodoptera frugiperda (J. E. Smith) is a notorious insect pest of poaceae and causes severe economic damage to major cereal crop. It has evolved with different levels of insecticide resistance. Insect cytosolic GSTs are a major class of detoxifying enzymes and have been implicated in metabolic resistance and protection against oxidative stress. In this study, an epsilon class GST ( SfGSTe9 ) was identified from S. frugiperda and its transcript levels were highest in the fat bodies, second instar and pupae. Furthermore, SfGSTe9 is upregulated after exposure to beta- cypermethrin, lambda -cyhalothrin, chlorpyrifos, and malathion. The kinetic analysis suggests the purified recombinant proteins exhibit CDNB conjugating activity, with the V max of 11.87 ± 0.25 μM·min −1 ·mg −1 protein and K m of 0.22 ± 0.01 mM. The peroxidase activity assays indicate that SfGSTe9 has antioxidant activity against both CHP and H 2 O 2. The inhibition assays infer that four types of insecticides have strong inhibition on the GST activity. In vitro metabolism assays with HPLC further suggest that SfGSTe9 could be able to deplete 11.2 %, 21.3 % and 19.3 % of beta- cypermethrin, lambda -cyhalothrin and chlorpyrifos within 2 h, respectively, with specific activity varying between 30 and 40 μM·min −1 ·mg −1 protein. However, no metabolites were identified in this case, indicating that SfGSTe9 probably involves in detoxification via binding and sequestration. 3D modeling and molecular docking analysis indicate that above three types of insecticide compounds fit nicely into the hydrophobic pocket in the active site of SfGSTe9 . Our results definitely demonstrate that SfGSTe9 of S. frugiperda plays pivotal role in insecticide detoxification and serves in defence against oxidative stress .

研究领域: 昆虫学 · 分子生物学 · 毒理学
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CATALYSIS COMMUNICATIONS · 2019 · IF 3.674

Discovery and application of methionine sulfoxide reductase B for preparation of (S)-sulfoxides through kinetic resolution

Yuanmei Wen,Liaotian Peng,Yang Zhou,Tao Peng,Yu Chen,Xiaoling Cheng,Yongzheng Chen,Jiawei Yang

Here we report a methionine sulfoxide reductase B (MsrB) enzymatic system for the preparation of ( S )-sulfoxides through kinetic resolution of racemic ( rac ) sulfoxides. Eight MsrB homologue recombinant proteins were expressed and their activities on asymmetric reduction of rac -sulfoxides were analyzed. Among these MsrB homologue proteins, one protein from Acidovorax species showed good activity and enantioselectivity towards several aryl-alkyl sulfoxides. The ( S )-sulfoxides were prepared with 93–98% enantiomeric excess through kinetic resolution at initial substrate concentration up to 50 mM. The establishment of MsrB catalytic kinetic resolution system provides a new efficient green strategy for preparation of ( S )-sulfoxides.

研究领域: 生物化学 · 合成生物学 · 绿色化学
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JOURNAL OF PHYSICS D-APPLIED PHYSICS · 2023 ·Vol. 56 ·期 49 ·495103 · IF 3.4

Boosting the open-circuit voltage of Cu2ZnSn(S,Se)4 solar cell by Cd/NH3 soaking

Yujiao Ma,Yuzhou Sun,Zihan Zhang,Haokai Zhao,Haifeng Gao,Qing Zhou,Wenbo Li,Xiaoyun Teng,Chao Gao,Wei Yu

In this paper, the open-circuit voltages (VOC) of Cu2ZnSn(S,Se)4 (CZTSSe) solar cells were improved by soaking the CZTSSe films in Cd/NH3 solutions before the deposition of buffer layers. The effects of Cd/NH3 soaking on the properties of CZTSSe films and solar cells were investigated in depth. We found Cd/NH3 soaking can promote downward band bending of the CZTSSe layer at the surface region. In addition, the Cd/NH3 soaking can eliminate the deep level acceptor in CZTSSe and decrease the density of the defects at the absorber/buffer interface. These effects can significantly reduce the carrier recombination in the depletion region of CZTSSe solar cells. As a result, the VOC of CZTSSe solar cells were increased from ∼460 mV to ∼480 mV, the efficiency of the best CZTSSe solar cell was increased from 10.2% to 11.6% by the Cd/NH3 soaking process.

研究领域: 材料科学 · 光伏技术 · 半导体物理
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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

3D ZnO hollow spheres-dispersed CsPbBr3 quantum dots S-scheme heterojunctions for high-efficient CO2 photoreduction

Yijie Wang,Hougang Fan,Xiaoyan Liu,Jian Cao,Huilian Liu,Xin Li,Lili Yang,Maobin Wei

Efficient electron transfer process and excellent CO 2 adsorption capacity are of great significance for improving CO 2 photoreduction efficiency. 3 D– 0 D ZnO/CsPbBr 3 S-scheme heterojunction hollow spheres were successfully prepared via a simple self-assembled process for efficient CO 2 photoreduction. Photocatalytic CO 2 reduction experiments showed that the ZnO/CsPbBr 3 had the excellent CO 2 photocatalytic conversion activity to CO, which was about 2.61 times higher than that of ZnO hollow micro-spheres and 1.9 times higher than that of pure CsPbBr 3 quantum dots (QDs). Photoelectrochemical characterization confirmed that the ZnO/CsPbBr 3 composite had good photoelectric conversion ability and carrier transfer ability, which was beneficial to the photocatalytic reaction. The suitable band gap structure and DFT calculation results showed that the formation of built-in electric field at the ZnO/CsPbBr 3 interface can greatly improve the S-scheme electron transfer ability, which can foster the CO 2 photoreduction. Besides, the introduction of 3D structure can improve the dispersion of CsPbBr 3 QDs and effectively enhance the CO 2 capture ability of the catalyst, which greatly promoted the CO 2 photoreduction reaction. The current work can present a novel S-scheme photocatalyst , which is looked forward to providing a certain perception into the advance of novel highly efficient CsPbBr 3 QDs-based photocatalysts for CO 2 resource utilization.

研究领域: 材料科学 · 环境科学 · 催化化学
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Sustainable Materials and Technologies · 2023 · IF 9.6

Amorphous carbon with N-S bond active center for enhanced capacitive contribution of potassium-ion batteries

Dandan Ouyang,Liuqian Yang,Ya-nan Wang,Yongsheng Li,Feng Yu,Jiao Yin

Carbon materials have great potential in achieving excellent potassium-ion batteries (PIBs), while the low theoretical capacity of carbon materials limits the application of potassium ion batteries . Here, we reported an amorphous porous carbon with rich N-S bonds (N-S/C) by simple self-assembly possess and pyrolysis possess. The prepared N-S/C material possesses plentiful N-S bonds, which can act as active center to enhance the electrochemical capacity and accelerate transport dynamics. In addition, abundant porous structure can increase the contact area between electrode materials and electrolyte to shortens the diffusion path of ion transport, thereby improving the rate performance. As PIBs anodes, the N-S/C material exhibits a markedly enhanced reversible capacity of 389 mAh g −1 at 50 mA g −1 , excellent cycling stability (188.8 mAh g −1 at 500 mA g −1 after 1000 cycles) and rate performance (105 mAh g −1 at 2 A g −1 ). Importantly, the in-situ Raman unravels a reversible mechanism that intercalation/deintercalation of K + into/from the N-S/C, and the electrochemical analysis shows the N-S bond can improve the capacitive activity and enable fast kinetics toward superior K + -storage. These results demonstrate a promising carbonaceous anode material for PIBs and may provide guidance for designing of electrode materials of PIBs.

研究领域: 材料科学 · 能源存储
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2021 · IF 19.503

Construction of S-scheme 0D/2D heterostructures for enhanced visible-light-driven CO2 reduction

Shuaiqi Gong,Xue Teng,Yanli Niu,Xuan Liu,Mingze Xu,Chen Xu,Lvlv Ji,Zuofeng Chen

Zero-dimensional quantum dots (QDs) and two-dimensional nanosheets represent two kinds of distinctive materials with unique properties. Here, we describe the fabrication of step-scheme ( i.e. S-scheme) 0D/2D heterostructure with InVO 4 QDs and g -C 3 N 4 (CN) ultrathin nanosheets for photocatalytic CO 2 reduction. The formation of S-scheme heterostructure facilitates the separation of electron-hole pairs and reduces the recombination of charge carriers. Moreover, the light-absorption edge of InVO 4 /CN is extended to 605 nm because of the strong visible light absorption of InVO 4 QDs. The 0D/2D hybrid enables highly selective photocatalytic reduction of CO 2 to CO (93.3 %) at a decent rate of 69.8 μmol g −1 h −1 under visible light irradiation. Density functional theory (DFT) results suggest that the formation of InVO 4 /CN heterostructure can enhance CO 2 adsorption/activation, stabilize COOH* intermediates and allow rapid CO desorption as the major product. This study opens up a new possibility for construction of novel S-scheme heterostructure for photocatalytic applications.

研究领域: 材料科学 · 环境科学 · 化学
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NANO · 2021 · IF 1.556

NiCo2S4/S Composites Used as Cathode Materials in Lithium-Sulfur Batteries with High Performance

Qian Zhang,Renxia Zhu,Chenyu Zhao,Runze Fan,Yong Zhang,Yurong Cai

Application of lithium-sulfur battery has been limited due to polysulfide dissolution, the insulating nature of sulfur and the volumetric strain produced during charge and discharge process. To improve the performance of Li-S batteries, two kinds of bimetallic sulfides of NiCo 2 S 4 with flaky (F-NiCo 2 S 4 ) and sea urchin-like (S-NiCo 2 S 4 ) structures were synthesized by using simple hydrothermal method, which were used as sulfur carriers in lithium-sulfur batteries and showed excellent electrochemical properties. At 0.2 C, both electrodes of F-NiCo 2 S 4 /S and S-NiCo 2 S 4 /S have high pristine discharge specific capacities of 986 mAh g − 1 and 959 mAh g − 1 . At high current density of 4 C, the F-NiCo 2 S 4 /S electrode still has a high pristine discharge specific capacity of 673 mAh g − 1 and a coulombic efficiency of 97.00%. The specific capacity can remain at 526 mAh g − 1 with a low average attenuation of 0.17% even after 130 cycles. The excellent electrochemical performances of the cathode material can be ascribed to the synergistic effect of tubular morphology, good electrical conductivity and strong adsorption ability of NiCo 2 S 4 matrix for polysulfide. The job provides a new scheme and material for application of lithium-sulfur batteries with high performance.

CAS / MDL: 12136-58-2
研究领域: 材料科学 · 能源存储与转换
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BIOMASS & BIOENERGY · 2022 · IF 5.774

Catalytic depolymerization of the dealkaline lignin over Co–Mo–S catalysts in supercritical ethanol

Guojun Hao,Hongying Liu,Zhibing Chang,Kechen Song,Xin Yang,Han Ma,Wenjing Wang

In this work, lignin depolymerization was examined over CoMo sulfide catalysts supported on different carriers in supercritical ethanol system. The temperature, time, MoS 2 and carrier effects on the lignin depolymerization were investigated. 95.76% liquefaction yield with negligible char was achieved over Co–Mo–S/ZrO 2 at 340 °C for 150 min. The liquid product was mainly composed of C 4 –C 8 alcohols, C 4 –C 10 esters and C 7 –C 10 aromatic compounds . The synergistic effect of active sites and acid-base sites on support played an important role in lignin depolymerization. Furthermore, the Co–Mo–S/ZrO 2 catalyst is reusable with 8% loss in liquefaction yield after 5 cyclic runs. We believe that acid/base carriers or additives that can promote the medium to generate abundant free radicals or ions to replace external hydrogen pressure are one of the prospects for the design of depolymerization lignin catalysts.

研究领域: 化学工程 · 可再生能源
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