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APPLIED CATALYSIS B-ENVIRONMENTAL · 2025 · IF 21.1

Construction of functionalized Pt-O-S bridge on Pt/TiO2 simultaneously enhancing the catalytic activity and sulfur resistance for CO oxidation

Cangpeng Shan,Qinwei Jia,Yan Zhang,Guoshuai Liu,Xinyu Hou,Yunchong Wang,Rui Han,Caixia Liu,Weichao Wang,Qingling Liu

Removing industrial source CO through catalytic oxidation and providing heat for denitrification units have significant economic and environmental benefits. Sulfur poisoning of catalysts is the bottleneck to stabilize the system operation. To overcome this problem, we fabricated sulfate modified Pt/TiO 2 by appropriate NH 4 HSO 4 deposition, which survived in the SO 2 environment with the concentration as high as 1000 ppm SO 2 , and exhibited an outstanding stability with over 90% CO conversion at 200 °C for 500   h under a typical steel sintering flue gas condition. Experimental and theoretical explorations confirmed that the electronic structure of PtO x clusters was optimized through Pt-O-S bridges after sulfate modification. The O 2p band center closer to the Fermi level and the smaller energy difference between Pt 5d and O 2p band centers led to more active lattice oxygen of PtO x clusters. The more stable π back bonding between Pt 5d and CO 2p and weaker hybridization between Pt and the π⁎ (Ssp2-Osp2)2 orbital of SO 2 indicated enhanced CO adsorption while weakened SO 2 adsorption on Pt sites. The above factors simultaneously improved the low-temperature activity and sulfur resistance for CO oxidation over sulfate modified Pt/TiO 2 . This work provides new insights for the design of sulfur-resistant catalysts and the understanding on the effect of sulfates on catalytic activity.

CAS / MDL: 13463-67-7 7803-63-6
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ADVANCED FUNCTIONAL MATERIALS · 2021 ·Vol. 32 ·期 10 ·2110335 · IF 18.808

High-Efficiency Sb2(S,Se)3 Solar Cells with New Hole Transport Layer-Free Back Architecture via 2D Titanium-Carbide Mxene

Hu Li,Limei Lin,Liquan Yao,Fengying Wu,Dong Wei,Guoliang Liu,Zhigao Huang,Shuiyuan Chen,Jianmin Li,Guilin Chen

MXene, a class of 2D materials of metal carbide or nitride, has attracted a lot of attention recently due to its excellent optical and electrical properties. In this work, titanium-carbide MXene (Ti 3 C 2 T x ) is introduced as a back electrode in Sb 2 (S,Se) 3 thin-film solar cells (FTO/CdS/Sb 2 (S,Se) 3 /MXene) for the first time, which displaces traditional carbon (C) and gold (Au) electrodes entirely. Impressively, thanks to its high conductivity, mild reflectivity, and flexible flake architecture, the MXene-based device performance outperforms typical C and Au electrodes by 153% and 77%, respectively. Specifically, the tunable work function of MXene and a beneficial Sb–O bond formed between Sb 2 (S,Se) 3 and MXene efficiently suppress the recombination and enhance charge transport by enjoying the unique merit of the rich terminal groups of MXene. As a result, the best efficiency of 8.29% of MXene-based Sb 2 (S,Se) 3 solar device is achieved, which represents the highest performance of noble metal and/or hole transport layer-free derived Sb 2 (S,Se) 3 solar cells to date. This result has revealed that MXene is a feasible material to substitute the back electrode in Sb-based solar cells to reach high efficiency, low cost, and high stability.

✓ 已验证 DOI 高影响因子
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APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Needle growth of Nb2O5 nanoparticles on BiOCl nanosheets to fabricate S-scheme heterojunction with oxygen vacancies for enhanced photooxidation of cyclohexane

Kuan Wang,Yi Wang,Dan Wang,Yuan-Xiao Du,Xin-Peng Li,Zhen-Hong He,Huan Wang,Weitao Wang,Yang Yang,Zhao-Tie Liu

The exploration of cost-efficient, environmentally friendly, and high-efficacy photocatalysts for the enhanced selective photooxidation of cyclohexane to KA oil (cyclohexanone (CHA-one) and cyclohexanol (CHA-ol)) is a pivotal challenge in the industrial realm. Herein, the present study focuses on the synthesis of needle-like S-scheme heterojunction photocatalysts with oxygen vacancies, which are achieved by the needle growth integration of nano-sized Nb 2 O 5 particles onto the BiOCl nanosheets. Remarkably, the 40 % Nb 2 O 5 /BiOCl composites exhibited superior performance in the solvent-free photooxidation of cyclohexane at room-temperature and under atmospheric pressure. The production yield of KA oil was 180.3 μmol (CHA-one/CHA-ol molar ratio = 3.5), and exceptional selectivity towards KA oil, reaching up to 99.3 %. The enhanced photocatalytic efficiency in cyclohexane oxidation can be attributed to the unique S-scheme heterogeneous interfaces with specific nanoneedle morphology, which result in the enhanced photonic absorption, effective charge carrier separation, a high density of oxygen vacancies, and the exposure of the highly reactive (001) plane of BiOCl. The excellent interfacial charge separation and transfer pathways of S-scheme heterojunction are disclosed by the in-depth EPR analysis and DFT calculations. These insights highlight the significant potential of the needle-like Bi-based S-scheme heterojunction photocatalysts for the efficient photooxidation of saturated alkanes.

CAS / MDL: 110-82-7 111-49-9
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2025 · IF 8.5

Reinforcing active sites and multi-empty orbitals on N, S, B co-doped lignin-based catalysts for rechargeable zinc-air batteries

Qiang Xiao,Xianliang Song,Xiaojuan Jin

The advancement of rechargeable zinc-air batteries (ZABs) faces significant challenges, particularly due to substantial polarization and the slow kinetics of the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Multi-element doping represents an effective strategy to address the deficiencies in catalytic activity and stability observed in single-atom catalysts. In this study, we prepare an activated lignin carbon catalyst doped with three elements (N, S, and B) via salt assisted (KOH), referred to as AL-NSB, with the aim is to achieve bifunctional catalysis through the synergistic interaction between the three elements to influence the distribution of the electron cloud and the extent of carbonaceous defects within the catalyst. The catalyst exhibits an ORR half-wave potential ( E 1 / 2 ) of 0.798 V relative to the reversible hydrogen electrode. The superior activity of AL-NSB results in a peak power density of 293.76 mW cm − 2 for the ZAB, along with an excellent cycle lifetime exceeding 1000 h, surpassing the performance of commercial Pt/C-RuO 2 catalysts. The findings of this study underscore the critical roles of N, S, and B in enhancing the activity and stability of both the oxygen reduction and evolution reactions.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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Journal of Water Process Engineering · 2025 · IF 6.7

Novel S-scheme loofah biochar/MoS2/g-C3N4 heterojunctions with efficient photogenerated carrier separation and transfer capability: Effect, mechanism and application

Yang Yu,Lichao Xu,Kaiyuan Xu,Yan Li,Hao Chen,Dongxu Zhang,Yuanzi Chen,Yue Liu,Wenyue Qi

The construction of S-scheme heterojunctions has drawn widespread attention within the photocatalysis field due to their capacity for efficient separation of photogenerated carriers, leading to excellent photo-oxidation-reduction performance. Herein, a novel S-scheme loofah biochar/MoS 2 /g-C 3 N 4 (LB/MS/CN) heterojunction was successfully constructed by ultrasonication in 50 % ethyl alcohol and heat treatment in N 2 atmosphere. Degradation experiments showed that the 5 % LB/MS/CN ternary photocatalyst had optimal photocatalytic efficiency (96.4 %) for the degradation of rhodamine B (RhB), and the reaction rate (k) of this photocatalyst (0.05420 min −1 ) was 5.4 times that of unmodified CN (0.01001 min −1 ). Ultraviolet-visible diffuse reflectance spectra, Mott-Schottky, and free radical trapping experiments suggested that the photogenerated carriers in LB/MS/CN were transferred through the S-scheme structure. Consequently, the co-catalytic action of LB and the synergistic impact of the heterojunction structure between CN and MS led to a reduced photogenerated carrier recombination rate. Furthermore, LB/MS/CN had outstanding stability and the capacity to maintain RhB degradation performance under various environmental conditions (H 2 PO 4 − , NO 3 − , SO 4 2− , HCO 3 − , NaCl, humic acid (HA), and real water), showing good promise for practical applications. Thus, this work provides a possible strategy for purifying wastewater under visible light.

✓ 已验证 产品关联 DOI 高影响因子
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BIORESOURCE TECHNOLOGY · 2013 · IF 4.75

Characterization of inulin hydrolyzing enzyme(s) in commercial glucoamylases and its application in lactic acid production from Jerusalem artichoke tubers (Jat)

Thai Ha Dao,Jian Zhang,Jie Bao

A high inulinase activity was found in three commercially available glucoamylase enzymes. Its origin was investigated and two proteins in the commercial glucoamylases were identified as the potential enzymes showing inulinase activity. One of the commercial glucoamylases, GA-L New from Genencor, was used for Jerusalem artichoke tubers (Jat) hydrolysis and a high hydrolysis yield of fructose was obtained. The simultaneous saccharification and lactic acid fermentation (SSF) of Jat was carried out using GA-L New as the inulinase and Pediococcus acidilactici DQ2 as the fermenting strain. A high lactic acid titer, yield, and productivity of 111.5   g/L, 0.46   g/g DM, and 1.55   g/L/h, respectively, were obtained within 72   h. The enzyme cost using the commercial glucoamylase as inulinase was compared to that using the typical inulinase and a large profit margin was identified. The results provided a practical way of Jat application for lactic acid production using cheap commercial glucoamylase enzyme.

✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2019 · IF 4.175

Construction of NiMoO4/CoMoO4 nanorod arrays wrapped by Ni-Co-S nanosheets on carbon cloth as high performance electrode for supercapacitor

Bo Yu,Guohua Jiang,Wangcong Xu,Cong Cao,Yongkun Liu,Na Lei,Uwamahoro Evariste,Pianpian Ma

The NiMoO 4 /CoMoO 4 nanorod arrays wrapped by Ni-Co-S nanosheets were successfully grown on the surface of carbon cloth (NCMOS@CC) by combining of hydrothermal and electrochemical deposition methods. And the as-prepared NCMOS@CC showed good flexibility. The obtained NCMOS@CC as electrode materials were tested in a three-electrode system, showing a pretty good specific capacitance of 778.1 F g −1 at a current density of 0.5 A g −1 and excellent rate capability using 1 M KOH as the electrolyte. The flexible asymmetric supercapacitors (FASCs) were further fabricated using NCMOS@CC as the positive electrode and activated carbon@carbon cloth (AC@CC) as the negative electrode. The fabricated FASCs exhibited a safe working range with a potential window of 0–1.6 V with a maximum energy density of 33.1 Wh Kg −1 at 0.25 A g −1 and maximum power density of 3195 W kg −1 at 4 A g −1 . The fabricated FASCs even bent at different angles still showed good flexibility and stable electrochemical properties . These performances enable the NCMOS@CC to be one of the potential flexible electrodes for using in flexible energy storage devices.

✓ 已验证 DOI 高影响因子
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NEW JOURNAL OF CHEMISTRY · 2017 ·Vol. 41 ·期 15 ·7613-7620 · IF 3.269

Exonuclease III-aided autonomous cascade signal amplification: a facile and universal DNA biosensing platform for ultrasensitive electrochemical detection of S. typhimurium

Qianqian Pei,Yu Wang,Su Liu,Yifei Qin,Xueqi Leng,Xuejun Cui,Jiadong Huang

In this study, a novel electrochemical biosensor based on exonuclease III (Exo III)-aided autonomous cascade signal amplification for ultrasensitive and highly specific detection of Salmonella typhimurium (S. typhimurium) has been reported. Herein, two duplex DNA probes were ingeniously designed. An Ap–Pr duplex probe was constructed as a recognition element by hybridizing an S. typhimurium aptamer (Ap) with a primer (Pr). A P–S duplex probe has been designed to contain a protruding DNA fragment at 5′-termini that has an identical sequence with Pr (the secondary Pr), a complementary duplex DNA that is used for blocking a signal-triggered probe (S), and an overhung nucleic acid segment at 3′-end that can anneal with Pr and form double-stranded DNA with a blunt 3′-terminus, thus initiating Exo III-aided amplification reaction. Upon sensing of the target S. typhimurium, the specific recognition of S. typhimurium and aptamer releases Pr, which anneals with the P–S duplex and triggers the Exo III cleavage reaction, accompanied by release of Pr, S, and secondary Pr. After this, the released Pr and secondary Pr anneal with other P–S duplex, which in turn triggers the Exo III-assisted cycling cleavage. Thus, large amounts of S are liberated, which hybrids with S* (DNA probe complementary to S); thereby, 5′-methylene blue (MB)-labelled DNA probe (MBP) folds into a hairpin structure with 5′-terminus close to electrode surface for efficient electronic transfer. Moreover, the S–S* hybrid duplex is specifically hydrolyzed by Exo III to liberate S, which accordingly results in the cycling cleavage of S*. Therefore, numerous MBP transform into a hairpin structure with electroactive MB close to the electrode surface; this generates significantly amplified electrochemical signal towards S. typhimurium detection. The present developed strategy exhibited high sensitivity towards S. typhimurium with a detection limit of 2.8 × 10 cfu mL−1. Furthermore, the proposed autonomous cascade signal amplification strategy can be easily extended for detection towards a wide spectrum of analytes including nucleic acid, proteins, and small molecules possessing their corresponding aptamers. Therefore, the developed Exo III-aided autonomous cascade signal amplification strategy might indeed provide a facile and universal tool for bioanalysis and clinical diagnosis.

✓ 已验证 DOI 高影响因子
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ChemElectroChem · 2022 ·Vol. 9 ·期 15 ·e202200474 · IF 4.782

A Multi-Functional Separator for Li-S Batteries: WS2@C Nanoflowers Catalyze the Rapid Recycling of Lithium Polysulfides by Polar Attraction

Fanxuan Xie,Man Xiong,Jiapeng Liu,Jingwen Qian,Tao Mei,Jinghua Li,Jianyin Wang,Li Yu,Jan P. Hofmann,Xianbao Wang

Graphical WS 2 @C nanoflowers modified polypropylene separator (WS 2 @C-PP) can effectively adsorb lithium polysulfides and catalyze their conversion on the adsorptive/electrocatalytic sites of WS 2 . The unique design of the carbon coating on the WS 2 maximizes the synergism of polarity and conductivity, benefiting the recycling of the active materials, while forming the uniform and stable modified layer. Featuring high theoretical capacity, environmental friendliness and low cost, lithium-sulfur (Li-S) batteries become promising alternatives to satisfy the growing demand for energy storage. To boost their energy density for practical application, modified separators are needed to suppress shuttle effects resulting from the solubility of lithium polysulfides (LiPSs). Herein, we modified traditional polypropylene (PP) separators with functional WS 2 @C nanoflower composites (WS 2 @C-PP). They can effectively adsorb LiPSs and catalyze their conversion on the edge sites of the WS 2 . Also, the unique construction of a carbon layer coating on the WS 2 nanoflowers combines active sites and conducting properties. The material benefits the reversibility of redox reactions and reutilization of active materials. With the WS 2 @C-PP separator, the cell displays improved cycling stability and rate performance. When cycling at 0.1 C, the cell discharges a capacity of up to 1475 mAh g −1 , and it contributes 943 mAh g −1 originally at 1 C, with a decay rate of only 0.07 % after 500 cycles. Our work highlights the potential of functional separators to advance the properties of Li-S batteries.

✓ 已验证 DOI 高影响因子
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COMPOSITES PART B-ENGINEERING · 2023 · IF 13.1

High graphitized N-doping porous carbon combined with bifunctional separator for the synergistic adsorption/conversion of polysulfides in Li–S batteries

Zirui Zhao,Shixun Yang,Mingwu Xiang,Jinkui Li,Dongyuan Lei,Junming Guo,Shulei Chou,Mingwei Yuan,Wei Bai,Xiaofang Liu

Inferior conductivity of sulfur and inevitable shuttle effect of polysulfides are major obstacle of commercial application for Li–S batteries. Balancing the relation between adsorption effect and polysulfides synchronous conversion on the surfaces of metal oxides is crucial. Herein, a combination strategy with graphitized porous carbon and bifunctional separator is proposed for the multiple suppression of shuttle effect by the synergistic adsorption and synchronous conversion of polysulfides. Silk cocoon derived in-situ N-doping porous carbon and nano-TiO 2 /Super P decorated bifunctional separator are prepared by simultaneous activation/carbonization and surface coating approach, respectively. The unique lamellar porous carbon and nano-TiO 2 effectively encapsulate active sulfur and immobilize polysulfides by the physical/chemical synergetic adsorption. The density functional theory calculations effectively testify that TiO 2 with exposed (101) plane shows high chemical affinity toward polysulfides. Especially the as-prepared porous carbon shows an ultrahigh degree of graphitization that enhances the electronic conductivity . The TiO 2 /Super P-coated conductive bifunctional separator not only accelerates the electron transmission but also synchronously facilitates the redox conversion of polysulfides adsorbed on the TiO 2 surface. Benefiting from the above structure merits, the optimized battery delivers high initial discharge capacity of 1311 mAh g −1 at 0.2C and good cycling stability with a low capacity decay of 0.037% per cycle at 1.0C as well as excellent rate capacity of 977 mAh g −1 at 2.0C. Even with 4.2 mg cm −2 , the discharge capacity of 697 mAh g −1 is still retained after 70 cycles at 0.1C. This combination strategy exploits a novel way for the design and preparation of advanced lithium-sulfur batteries.

✓ 已验证 DOI 高影响因子
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CEMENT & CONCRETE COMPOSITES · 2023 · IF 10.5

Effects of different nanomaterials on the early performance of ultra-high performance concrete (UHPC): C–S–H seeds and nano-silica

Zhongtao Luo,Tianyi Zhi,Xiaohai Liu,Kunpeng Yin,Han Pan,Hu Feng,Yatao Song,Yanfeng Su

The early hydration of UHPC can be retarded by the low water/binder ratio, the high polycarboxylate superplasticizers dosage, and the large supplementary cementitious materials (SCM) content. In this study, the effects of the prepared nanoscale C–S–H seeds and nano-silica (NS) on the early performance of UHPC were compared. The mechanism of nanomaterials influencing the early hydration of UHPC was further characterized by calorimetry , thermal analysis, nuclear magnetic resonance (NMR), and mercury intrusion porosimetry . The results showed that the 1-day compressive strength of UHPC samples with 0.3 wt% C–S–H seeds and NS increased by 457% and 25% respectively compared to the control sample. Compared to NS, C–S–H seeds were more effective in accelerating the early (before 3 d) hydration to produce hydrates and refine the pore structure of UHPC. The NMR results further implied that compared with the NS, the C–S–H seeds was 12% and 343% more efficient in accelerating the early hydration of cement and SCMs, respectively. However, the performance enhancement of nanomaterials was effective at 1 d and had little effect thereafter.

✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

S-doped TiO2 photocatalyst for visible LED mediated oxone activation: Kinetics and mechanism study for the photocatalytic degradation of pyrimethanil fungicide

Tao Li,Amal Abdelhaleem,Wei Chu,Shengyan Pu,Fei Qi,Jing Zou

The degradation of pyrimethanil (PYR) was investigated through the activation of oxone by the S-TiO 2 (ST) photocatalyst under visible LED irradiation. The catalyst characterization revealed that the sulfur doping mechanism was based on the cation (S 6+ ) substitution of Ti 4+ in TiO 2 lattice. The optimal molar ratio of S/Ti at 0.25 was proven efficient in the PYR degradation. Influences of various reaction parameters including ST loading, oxone dosage, PYR concentration, and initial solution pH were examined. SO 4 •- , • OH, 1 O 2 , O 2 •- , and h + were found to be the reactive species generated in the ST/Oxone/Vis LED process. Different natural water constituents exerted dissimilar effects because of the generation of additional reactive species or their radical scavenging capabilities. Moreover, the reusability test indicates the ST photocatalyst is reusable and stable. A series of degradation intermediates was detected via four major degradation pathways. Overall, the ST/Oxone/Vis LED process was demonstrated to be a promising approach for the removal of organic pollutants.

✓ 已验证 DOI 高影响因子
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