Cell Reports
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2024
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IF 7.5
Mingzhi Wu,Xiaojun Zhou,Xinyi Zhou,Genxin Wang,Yiqun Zeng,Jun Li,Edward V. Prochownik,Fubing Wang,Youjun Li
Cholesterol metabolism reprogramming plays essential roles in hepatocellular carcinoma (HCC). However, precisely how cholesterol metabolism is dysregulated is not clear. Here, we show that the palmitoyltransferase ZDHHC3 and depalmitoylase ABHD17A regulate HCC cell cholesterol biosynthesis by dynamically S-acylating SREBP cleavage-activating protein (SCAP). SCAP S-acylation by ZDHHC3 at C264 antagonizes HACE1-mediated SCAP ubiquitination. Intriguingly, SREBP2 transcriptionally upregulates ZDHHC3 to form a positive feedback loop, which explains why negative feedback regulation of SCAP/SREBP2 signaling fails in HCC. Increased cholesterol in the tumor microenvironment (TME) restrains CD4 + T cell cytotoxicity. Hence, the cholesterol metabolism reprogramming and cholesterol level alternation in the TME cooperate to promote HCC development. We identified a small-molecule inhibitor of ZDHHC3 that, combined with anti-PD-1 immunotherapy, inhibited diethyl nitrosamine (DEN)/CCl 4 -induced HCC growth in mice. ZDHHC3-mediated SCAP S-acylation reprograms cholesterol metabolism and promotes HCC immune escape. ZDHHC3 is thus identified as a rational chemotherapy target for HCC.
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PHYSICAL CHEMISTRY CHEMICAL PHYSICS
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2024
·Vol. 26
·期 29
·19658-19672
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IF 2.9
Yaqi Liu,Guicheng Luo,Yichen Liu,Zuozheng Xu,Hengxin Shen,Yuxiang Sheng,Yuan Zhu,Shuyi Wu,Lizhe Liu,Yun Shan
Photocatalytic degradation of organic pollutants in water is of great significance to the sustainable development of the environment, but encounters limited efficiency when a single compound is used. Thus, there have been enormous efforts to find novel photocatalytic heterostructured composites with high performance. In this work, a novel S-scheme heterostructure is constructed with BiOBr and Zn2+ doped C4N3 (Zn–C4N3) by a solvothermal method for efficient photodegradation of tetracycline (TC), a residual antibiotic difficult to be removed from the aquatic environment. Thanks to Zn2+-doping induced improvement in chemical affinity between Zn–C4N3 and BiOBr, well-formed Zn–C4N3/BiOBr heterostructured hollow spheres are formed. This structure can efficiently suppress fast recombination of photogenerated electron–hole pairs to enhance the photocatalytic activity of BiOBr dramatically. At a room temperature of 25 °C and neutral pH 7, the catalyst can degrade a significant portion of TC pollutants within 30 min under visible light. Also, the Zn–C4N3/BiOBr heterostructure displays good stability after recycling experiments. Free radical capture experiments and ESR tests show that ˙O2− is the main active substance for photocatalytic degradation of TC. This study provides new insights for constructing heterostructures with an intimate interface between the two phases for photocatalytic applications.
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Nano Materials Science
·
2025
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IF 17.9
Yang He,Qingling Ruan,Han Kang,Ling Ye,Ya-Xiong Wang,Tiefeng Liu,Hairong Cheng,Xingxing Gu
Li-S batteries (LSBs), with their exceptional theoretical energy density, are widely recognized as a leading option for future energy storage solutions. Nevertheless, on the way to commercialization, the poor conductivity of the positive electrode, the easy dissolution loss of the active substance, and the serious dendrite growth of the negative electrode are stumbling blocks. Therefore, this work designs a novel tungsten and nitrogen-co-doped nanoporous carbon (W,N-C) with multifunction: chemically adsorbs the polysulfides to inhibit shuttling behavior, accelerates Li + transfer, and catalyzes polysulfides redox to address the aforementioned issues of LSBs. As expected at the beginning of the design, the prepared W,N-C-5/S composites cathodes demonstrate excellent performances, i.e., delivering an initial capacity of 944.9 mAh g −1 and a reversible capacity of 771.7 mAh g −1 after 500 cycles at 1 C, significantly outperforming the N-C/S contrast sample. The proposed method offers a feasible solution for boosting the electrochemical performance of LSBs.
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INORGANIC CHEMISTRY COMMUNICATIONS
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2024
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IF 4.4
Huadong Liu,Hao Sun,XiaoYu Sun,Jing liang Cheng
This paper presents a novel tubular microreactor immobilized a photocatalyst to overcome the limitations of low light utilization and the challenges associated with catalyst recovery in traditional photocatalysis reactors. The copper-sulfur co-doped carbon quantum dots (Cu, S-CQDs)/bismuth vanadate (BiVO 4 ) composites were successfully immobilized on the inner surface of the microreactor channel through the sol–gel process. The catalytic layer in the microreactor enlarged the specific surface area and facilitated the mass transfer. Meanwhile, it also greatly reduced the consumption of chemical supplies and eliminated the need for recycling the photocatalyst. The morphology and structural features of the catalytic layer were studied by characterization. Then the photocatalytic performance of the microreactor was evaluated by photocatalytic degradation of Rhodamine B. The photocatalytic kinetics of the photocatalytic reaction in the microreactor was 0.60925, which was 10.49 times greater than that in the macroscopic system. The results showed that the microreactor led to a significant improvement in degradation efficiency. The reproducibility experiments conducted on the microreactor system further demonstrate its excellent stability. In short, integrating the beneficial properties of microreactors with Cu, S-CQDs/BiVO 4 exhibits highly promising prospects of photocatalytic applications.
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CHINESE JOURNAL OF CATALYSIS
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2025
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IF 17.7
Xinyue Tan,Minghui Zhang,Yang Bai,Xiaoyu Liu,Jianfang Jing,Yiguo Su
The major challenge in photocatalytic water splitting lies in water oxidation reactions, which still suffer from poor charge separation. This study overcame inefficient charge separation by establishing a robust interfacial electric field through the electrostatic-driven assembly of Co 3 O 4 nanoparticles with a perylene imide supramolecule (PDINH). The well-aligned band structures and intimate interfacial contact in the PDINH/Co 3 O 4 heterostructure create an enhanced interfacial electric field that is 4.1- and 53.2-fold stronger than those of individual PDINH and Co 3 O 4 , thus promoting directional charge separation and transfer. Moreover, S-scheme charge transfer strongly preserves the oxidative holes in PDINH to drive efficient water oxidation reactions. Consequently, PDINH/Co 3 O 4 composite achieves a photocatalytic oxygen evolution rate of 29.26 mmol g –1 h –1 under visible light irradiation, 8.2-fold improvement over pristine PDINH, with an apparent quantum yield of 6.66% at 420 nm. This study provides fundamental insights into interfacial electric field control for the development of high-performance organic photocatalysts for efficient water oxidation.
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Scientific Reports
·
2025
·Vol. 15
·期 1
·1-13
·
IF 3.9
Fan Xinyu,Zhang Ying,Li Xinyu,Ding Junhui,Huang Jiaolong,Lian Kai,Duan Peng,Hu Chunhui,Xu Junchang
In this study, the effects of Ginsenoside Rg1 (Rg1), the primary bioactive constituent of Panax ginseng roots, on glucocorticoid-induced osteoporosis (GIOP) were examined using a zebrafish model, with a focus on elucidating its underlying mechanisms. Our findings demonstrated that Rg1 treatment inhibited osteoporosis induced by methylprednisolone (PN), as evidenced by increased mineralisation area and integrated optical density in the spine and skull of zebrafish larvae. Rg1 reduced the expression of bglap (an osteogenic marker gene) and increased the expression of traf (an osteoclast marker gene) compared with the PN group. Behavioural analysis revealed that Rg1 alleviated PN-induced hypoactivity, resulting in enhanced motion speed. Furthermore, transcriptome analysis identified 383 genes reversed by Rg1 treatment, with significant enrichment in skeletal system development. KEGG analysis indicated that Rg1 influenced several signalling pathways primarily involved in retinol, fat, protein and lipid metabolism. Several genes related to skeletal system development and retinol metabolism were validated by qRT-PCR. In summary, this study provides scientific evidence for the potential mechanisms of Rg1 in the therapeutic intervention of GIOP, highlighting its promise as a potential pharmacological agent for the prevention and treatment of osteoporosis.
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Membranes
·
2025
·Vol. 15
·期 8
·231
·
IF 3.6
Zhuangzhuang Tian,Yun Yin,Jiandong Wang,Xiuling Ao,Daijun Liu,Yang Jin,Jun Li,Jianjun Chen
Nanofiltration (NF) is considered a competitive purification method for acidic stream treatments. However, conventional thin-film composite NF membranes degrade under acid exposures, limiting their applications in industrial acid treatment. For example, wet-process phosphoric acid contains impurities of multivalent metal ions, but NF membrane technologies for impurity removal under harsh conditions are still immature. In this work, we develop a novel strategy of acid-resistant nanofiltration membranes based on interfacial polymerization (IP) of polyethyleneimine (PEI) and cyanuric chloride (CC) with the s-triazine ring. The IP process was optimized by orthogonal experiments to obtain positively charged PEI-CC membranes with a molecular weight cut-off (MWCO) of 337 Da. We further applied it to the approximate industrial phosphoric acid purification condition. In the tests using a mixed solution containing 20 wt% P2O5, 2 g/L Fe3+, 2 g/L Al3+, and 2 g/L Mg2+at 0.7 MPa and 25 °C, the NF membrane achieved 56% rejection of Fe, Al, and Mg and over 97% permeation of phosphorus. In addition, the PEI-CC membrane exhibited excellent acid resistance in the 48 h dynamic acid permeation experiment. The simple fabrication procedure of PEI-CC membrane has excellent acid resistance and great potential for industrial applications.
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ACS Nano
·
2025
·
IF 16
Yu Liu,Lu Wu,Yong Wang,Le-Wei Shen,Ge Tian,Lianmeng Cui,Ling Qin,Liang Zhou,Yuexing Zhang,Federico Rosei,Xiao-Yu Yang
Electrolysis of seawater for hydrogen (H2) production to harvest clean energy is an appealing approach. In this context, there is an urgent need for catalysts with high activity and durability. RuO2 electrocatalysts have shown efficient activity in the hydrogen and oxygen evolution reactions (HER and OER), but they still suffer from poor stability. Herein, surface S-doped nanostructured RuO2 (S-RuO2) is rationally fabricated for efficient overall seawater splitting. Doping with S enhances the activity (overpotentials of 25 mV for the HER and 243 mV for the OER), long-term durability (1000 h at 100 mA cm–2), and achieves nearly 100% Faraday efficiency (FE). Moreover, the S-RuO2-based anion exchange membrane seawater electrolyzer requires 2.01 V to reach 1.0 A cm–2 under demanding industrial conditions. Experimental analysis and theoretical calculations indicate that surface S introduction could lower the valence state of Ru, thereby conferring enhanced activity and stability. Furthermore, the nanostructured S-RuO2 electrocatalyst is highly protected by the S-doped surface, which repels Cl– in alkaline seawater. This investigation presents a feasible strategy for designing RuO2-based seawater splitting catalysts with both high performance and good resistance to anodic corrosion.
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POLYMER
·
2024
·
IF 4.1
Chunlei Xu,Hang Guo,Changzhu Lv,Wei Chen,Liangbin Li,Kunpeng Cui
Understanding on the structure and dynamics of poly(vinyl acetal)s is insufficient due to the complicated chemical structure and amorphous nature of this type of polymers. In this work, we investigate the effect of side group length on structure and dynamics heterogeneity at different length scales spanning from side group, segment, and polymer network by combing dynamic mechanical analysis (DMA), dielectric relaxation spectroscopy (DRS), solid-state NMR, and differential scanning calorimetry analysis (DSC). By increasing the length of acetal side group, its intrinsic dynamics slows down. Taking into account the scale of segment and networks, with the increase of acetal group length, the formation of cross-linking sites formed by the hydroxyl-rich domain is suppressed, the relaxation distribution of the segment widens, and the volume fraction of rigid component decreases. The effect of side group length on the structure and dynamics heterogeneity of poly(vinyl acetal)s at different scales results in significant changes in material properties such as the non-monotonic change in loss factor value (tan δ ) and a monotonous reduction in glass transition temperature ( T g ).
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CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Kai An,Hongyan Jia,Ruobing Cheng,Yong Guo,Xiaohui Liu,Yanqin Wang
Pt-based bimetallic catalysts have gained more and more attention in propane dehydrogenation (PDH), but still suffer from the high cost and poor stability. In this work, a PtCu@S-1 catalyst with an extremely low loading of Pt (0.047 wt%) is prepared by in-situ hydrothermal synthesis and employed in PDH. An excellent productivity (propylene yield: 471.8 molC 3 H 8 ⋅ g Pt -1 ⋅ h −1 ) is achieved at 600 °C with a weight hour space velocity of 25.80 h −1 . After 50 h of reaction at 600 ℃, 0.047Pt0.19Cu@S-1 catalyst still remains sinter-free, with a deactivation rate of only 0.006 h −1 . Various characterizations show that Cu 0 co-existed with Pt 0 in PtCu@S-1 catalyst plays an important role, greatly improved catalyst reactivity and stability. At high weight hour space velocity (44.5 h −1 ), the propylene productivity can reach 1056.4 molC 3 H 8 ⋅ g Pt -1 ⋅ h −1 . This work provides a new way for the design of extremely low Pt-loaded PDH catalysts with excellent performance at high temperatures.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Yukang Fan,Fangbao Fu,Dongjie Yang,Weifeng Liu,Xueqing Qiu
Constructing heteroatom-doped porous carbons with distinct charge storage properties is significant for high-energy–density supercapacitors, yet it remains a formidable challenge. Herein, we employed a thiocyanogen-modulated alkali activation strategy to synthesize N and S co-doped lignin hierarchical porous carbon (NSLHPC). In this process, thiocyanogen serves as a surface modulation mediator to substitute oxygen with nitrogen and sulfur species, while the combination of KOH activation and MgO template generates numerous nanopores within the carbon structure. The three-dimensional interconnected nanosheet architecture facilitates rapid ion transfer and enhances accessibility to active sites. Density functional theory (DFT) calculations demonstrate that introducing N and S heteroatoms through oxygen substitution reduces the adsorption energy barrier of Zn 2+ . Consequently, the optimized NSLHPC exhibits a remarkable specific capacitance of 438F/g at 0.5 A/g in 6 M KOH, delivering an energy density of 10.4 Wh/kg in the symmetric supercapacitor and an impressive energy density of 104.9 Wh/kg in the zinc-ion hybrid capacitor. The NSLHPC cathode also shows an excellent lifespan with capacitance retention of 99.0 % and Columbic efficiency of 100 % over 10,000 cycles. This study presents innovative strategies for engineering high-performance porous carbon electrode materials by emphasizing pore structure modulation and N, S co-doping as crucial approaches.
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Advanced Energy Materials
·
2020
·Vol. 10
·期 25
·1904026
·
IF 25.245
Wenqiang Wang,Dongya Wang,Guiyou Wang,Mengyao Zheng,Gengchao Wang
The shuttle of polysulfide and severe volume change of sulfur cathodes, are the bottlenecks in the practical application of lithium–sulfur batteries, and need to be solved through further exploration of simple and scalable strategies. Herein, an elastic and conductive coating layer is designed and synthesized, by combining water soluble conducting polymer modified carbon nanotubes (PASANTs) with crosslinked waterborne polyurethane ( c WPU). It shows high electronic conductivity and excellent resilience. As a result, a lithium–sulfur battery with c WPU/PASANTs coated cathode is able to achieve an outstanding cycle stability with a capacity of 70.8% after 500 cycles at 0.5C and an excellent rate performance (specific capacity of 1130 mAh g −1 at 0.1C and maintain 68.2% at 2C). This work embodies a systematic design concept, which shows the application prospects of large-scale production, and is expected to be further applied to other easily pulverized high-specific-capacity materials such as silicon and tin.
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