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JOURNAL OF POWER SOURCES · 2024 · IF 8.1

Stable and eco-friendly Ag–In–S/Zn–S quantum dots for an efficient and optically transparent luminescent solar concentrator-organic photovoltaic system

Kanglin Yu,Yuanyuan Xiao,Shiqi Hu,Xufan Zheng,Bowen Gao,Jingjing Xu,Zongzhe Li,Ruike Zhou,Yaowen Hu,Qingliang You,Biao Xiao,Renqiang Yang

Quantum dot (QD) based luminescent solar concentrator-organic photovoltaic (LSC-OPV) systems demonstrate significant potential in applications including building-integrated photovoltaics (BIPV). In this study, eco-friendly Ag–In–S/Zn–S QDs with a high photoluminescence quantum yield (PLQY = 73 %) are synthesized using a simple hydrothermal method. The influence of Zn-S precursor reactivity on QD properties is studied. The synthesized QDs exhibit excellent stability over a wide temperature range (90–360 K). The Ag–In–S/Zn–S LSCs maintain over 90 % of their initial PLQY after a two-month exposure to natural sunlight. Additionally, the power conversion efficiency (PCE) of the fabricated LSC-OPV system reaches 1.00 % under near-actual condition (9 mW cm −2 ). Moreover, when the irradiation intensity is further decreased to 0.4 mW cm −2 , the LSC-OPV system shows a PCE as high as 5.27 %, demonstrating that the LSC-OPV system can operate efficiently at low illumination intensities. Notably, the fabricated LSCs have minimal impact on the incident sunlight spectrum, making them suitable for BIPV applications. Thus, this study is a first that is known to report the integration of eco-friendly QD-based LSCs with organic photovoltaic cells, which positively contributes to the advancement of BIPV.

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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Hyperbranched organosulfur polymer cathode materials for Li-S battery

Pengfei Sang,Jiahan Song,Wei Guo,Yongzhu Fu

Organosulfur polymers are a unique class of cathode materials for rechargeable lithium batteries. They are abundant, rich in structure, and easy for synthesis. Here, we report a new class of organosulfur polymers synthesized by condensation reactions between 1,3,5-benzenetrithiol (BTT) and elemental sulfur with three different molar ratios ( i.e. , 1:1.5, 1:3.0, and 1:4.5) in carbon disulfide solution without heating and additional catalyst. Removal of H 2 S leads to the linkage of S-S bonds, forming hyperbranched polymers. When the BTT: sulfur molar ratio is 1:4.5, the polymer has a high theoretical specific capacity of 901.7 mAh g −1 . We have studied their structures and compositions through a series of material characterizations, and conducted an in-depth discussion on their electrochemical behavior in rechargeable lithium batteries. Excellent cycling performance of these materials shows great potential for practical application.

研究领域: 材料科学 · 电化学 · 能源存储
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Cell Reports · 2026 ·Vol. 45 ·期 9 · IF 7.7

Dynamic S-acylation of IDH2 regulates mitochondrial redox homeostasis

Chen Miao,Zhen Wang,Jian Lin,Ziye Zhu,Jinan Wang,Baoen Chen

Mitochondrial redox homeostasis is fundamental for cellular function, and its dysregulation is associated with various diseases, including cancer. Isocitrate dehydrogenase 2 (IDH2) is a key enzyme that maintains this balance by generating NADPH. However, the mechanisms controlling IDH2 subcellular localization remain incompletely understood. Here, we identify reversible S-acylation as a critical regulator of IDH2 localization. Using chemical reporters, we demonstrate that IDH2 is S-acylated at a conserved cysteine residue, mediated by ZDHHC3 and APT1. Loss of IDH2 S-acylation disrupts its mitochondrial localization by reducing its interaction with the mitochondrial import receptor TOMM20, leading to NADPH deficiency, redox imbalance, and impaired oxidative phosphorylation. Consistently, ZDHHC3 knockout phenocopies IDH2 S-acylation deficiency, impairing its mitochondrial localization and function. Genetic ablation of IDH2 S-acylation suppresses tumor growth in vitro and in vivo . Our work establishes dynamic S-acylation of IDH2 as an essential regulator of mitochondrial redox homeostasis, thereby revealing a potential metabolic vulnerability in cancer.

CAS / MDL: 637-39-8
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DYES AND PIGMENTS · 2022 · IF 5.122

A bistable electrochromic device based on poly(viologen)s

Yuewei Zhang,Xuchao Jin,Weiran Zhang,Chang Gu,Xuesong Liu,Yu-Mo Zhang

A bistable electrochromic device based on poly(viologen)s is demonstrated with good overall performance, including bistability (4981 s), switch-on voltage (−1.0 V) and reversibility (≥1000 cycles). Overall, these results imply that the control of the diffusivity of viologens is an effective methodology for achieving excellent bistability and low energy consumption.

研究领域: 材料科学 · 电化学
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MACROMOLECULES · 2022 · IF 6.057

Magnetic Poly(ionic liquid)s: Bottlebrush versus Linear Structures

Jiangli Li,Shengqi Ji,Xiaoliang Yu,Xiaoyan Yuan,Ke Zhang,Lixia Ren

Magnetic poly(ionic liquid)s (MPILs) with FeCl4– as counterions show phase transition from paramagnetism to ferromagnetism by introducing strong π–π stacking groups. The neighboring Fe(III)–Fe(III) distance and the ordering degree of magnetic ions are crucial for the phase transition. In this work, linear and bottlebrush magnetic polymers are synthesized to study the effect of topological structure on the magnetic property of MPILs. Magnetic studies show that the bottlebrush MPILs are ferromagnetic at low temperature while the linear analogue is paramagnetic. With increasing of the grafting ratio, the phase transition temperature from paramagnetism to ferromagnetism is increased. Compared with linear structure, the bottlebrush polymers show high ordering and crowding of the side chains which are favorable to the ferromagnetic phase transition.

CAS / MDL: 3030-47-5
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POLYMER · 2026 · IF 5.1

Cationic Oligo(α-lipoic acid)s for Antifungal Therapy

Zhiqi Lin,Wenjie Zhou,Zijian Yang,Chao Chen,Yihan Qiu,Yiyun Cheng,Mingquan Chen,Jingjing Hu

Fungal infections remain a major health burden due to limited treatment options, biofilm-associated tolerance, and increasing emergence of drug-resistant strains. Antifungal polymers have gained growing interest because their molecular structures can be rationally tuned to optimize antifungal activity. Herein, we prepared a series of side-chain-functionalized oligo(α-lipoic acid)s and identified the primary amine-bearing oligomer OLA-EDA as the lead candidate, based on its favorable balance between antifungal activity and cytocompatibility. Mechanistic assays showed that OLA-EDA induced relatively limited fungal membrane depolarization and permeabilization, but markedly increased intracellular reactive oxygen species (ROS) levels. NAC pretreatment partially rescued fungal viability, supporting the involvement of oxidative stress or redox imbalance in the OLA-EDA-mediated antifungal activity. In addition, OLA-EDA inhibited hyphal development and biofilm formation and downregulated related virulence-associated genes. In murine vulvovaginal candidiasis model, OLA-EDA treatment reduced fungal burden and alleviated local inflammation, indicating its potential for topical antifungal therapy.

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Communications Biology · 2026 · IF 5.8

ZDHHC4-mediated S-palmitoylation of CD276 promotes breast tumorigenesis

Liu Lu,Wang Zhuolin,Xiang Qin,Rong Huan,Xie Chunyang,Tian Rui,Zheng Zeze,Xu Ruqing,Mei Ligang,Song Jiong,Lin Changhai,Yang Feng,Huang Xue,Xiang Tingxiu,Yang Aimin

Protein S -palmitoylation is catalyzed by a family of zinc finger Asp-His-His-Cys (ZDHHC) domain-containing palmitoyl acyltransferases, most of which are widely expressed in normal tissues and aberrantly increased in diverse malignant tumor tissues. However, the mechanisms of action of S -palmitoylation in tumor development are not fully understood. Here we profile interacting proteins of ZDHHC4, a member of the ZDHHC family, and further characterize the immune checkpoint CD276 as a substrate of ZDHHC4. ZDHHC4 mediates S -palmitoylation of CD276 at Cys488 and Cys496, which is reversed by palmitoyl-protein thioesterases (PPT1/2). Consequently, S -palmitoylation enhances the plasma membrane targeting of CD276 and increases its protein stability. Moreover, S -palmitoylation of CD276 promotes breast cancer cell proliferation and migration, and contributes to tumor growth in murine xenograft models. Thus, our study reveals an important molecular mechanism of S -palmitoylation in the regulation of CD276 function, highlighting the therapeutic potential of targeting ZDHHC4-CD276 signaling axis in breast cancer.

CAS / MDL: 51805-45-9
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Sensing and Bio-Sensing Research · 2015 · IF 0

Detection of S-nitrosylated protein by surface plasmon resonance

Ruirui Wang,Qingnan Kong,Jie Zhou,Lili Zhang,Shuhua Zhu

S -Nitrosylation has recently emerged as an important posttranslational modification of proteins and is becoming an intensive field of research in plants. Protein S -nitrosation, a reversible post-translation modification of cysteine, affects many cell signaling pathways and plays critical roles in redox-sensitive cell signaling. Changes in protein function effectively transmit biological signals and thus provide a framework for elucidating signaling networks. This paper presented a new, universal immunosensor for detection of S -nitrosylated proteins. Electrochemical impedance spectroscopy (EIS) and atomic force microscope (AFM) were used to estimate the formation of self-assembled film. This method was based on the specific binding characteristics of biotin–streptavidin, using Biotin-HPDP labeled protein sulfhydryl group as the substrate to detect proteins. The sensor was used to detect bovine serum albumin (BSA), nitrosylated BSA and denitrosylated BSA. The results showed that 90.61% of nitrosylated BSA were reduced, verifying that protein S -nitrosylation is a reversible and effective post-translation modification. This method was successfully applied to detect S -nitrosylated protein in Feicheng peach. The results showed good repeatability and precision. This method provided a molecular basis for further exploring the mechanism of S -nitrosylation of proteins in plants.

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Journal of Materials Chemistry A · 2025 · IF 9.5

Bi2WO6/COF S-scheme heterostructure photocatalyst for H2O2 production

Han Liu,Jun Zhang,Quanlong Xu,Hong Tao,Tingmin Di,Quanrong Deng,Shenggao Wang

Artificial photosynthesis offers a viable strategy for sustainable and environmentally friendly H2O2 production. However, conventional inorganic semiconductor photocatalysts often face limitations such as restricted light absorption, inadequate redox ability, small specific surface area and poor stability, which greatly restrict their practical applications. Herein, an innovative inorganic/organic S-scheme heterojunction is fabricated by an electrostatic self-assembling method. The optimized BT-12 composite demonstrates a significantly enhanced photocatalytic H2O2 production rate of 723 μmol L−1, surpassing the rates achieved by pure Bi2WO6 and TpPa-Cl-COF by factors of 10 and 2.9, respectively. This improvement can be attributed to the synergistic effects of enhanced light absorption, increased specific surface area, and effective separation of charge carriers and redox active sites, as well as the strong redox ability induced by the S-scheme heterojunction. Density functional theory (DFT) calculations along with X-ray photoelectron spectroscopy (XPS) measurements and electron paramagnetic resonance (EPR) characterization confirm the step-by-step charge transfer pathway. The active species trapping experiments validate that H2O2 is predominantly produced by a two-step one-electron process. This work highlights an innovative and promising strategy for constructing a highly efficient photocatalytic system based on inorganic/organic heterojunctions.

CAS / MDL: 34374-88-4 615-66-7
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ACS Applied Nano Materials · 2024 · IF 5.3

N/S Dually Doped Nanoporous Carbon for CO2 Adsorption

Jun Xiu Chen,Agul Bao,Dalai Siqin

In this study, we prepared N/S-codoped porous carbon materials via a one-step doping method using lignin as the carbon source, thiourea as the N and S source, and KOH as the activator. The synthesized material exhibited a rich N content and a certain S content. The important reason the CO2 adsorption characteristic of the carbon materials were investigated by modulating the thiourea proportion and doping temperature. Results indicate that at a thiourea ratio of 1:4 and a doping temperature of 700 °C, the material exhibited an outstanding CO2 adsorption capacity of 3.49 mmol/g. Various characterizations revealed that such a high adsorption capacity is attributed to the combination of a microporous structure and excellent surface chemical properties. The doping of S atoms resulted in the formation of effective active sites, increased the defect density of the material, and promoted the generation of N functional groups, thereby enhancing the efficiency of CO2 adsorption. In addition, the material exhibits high CO2/N2 selectivity and cycling stability. The overall results indicate that lignin-derived N/S-codoped porous carbon can serve as a potential adsorbent for CO2 capture.

CAS / MDL: 9005-53-2 62-56-6
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Chemistry-An Asian Journal · 2025 · IF 3.3

Gold Nanoparticles-Based Colorimetric Assay for Cathepsin S Activity

Xianghan Li,Hongyan Shu,Xinna Xu,Yalan Wang,Lingzhi Zhao,Ying Liu,Juanjuan Peng

Cathepsin S (CatS) is a lysosomal enzyme belonging to the papain family of cysteine proteases. Studies have demonstrated that CatS plays a pivotal role in antigen presentation and is associated with Alzheimer's disease, atherosclerosis, and obesity, positioning it as a potential target in related disorders. Consequently, the development of a selective and straightforward method for detecting CatS is crucial. In this study, we introduce a colorimetric approach utilizing gold nanoparticles (AuNPs) and CatS-specific peptides for the detection of CatS activity. The CatS enzyme cleavage peptides, PMGAPC or PMGAPC-NH 2 , can stabilize AuNPs in a hydrosaline solution without aggregation. Upon hydrolysis of PMGAPC or PMGAPC-NH 2 by CatS, the AuNPs aggregate with a color change from red to blue. After optimizing the size of the AuNPs and the concentration of the peptides, the limits of detection for CatS were both to be 10 nM, when PMGAPC or PMGAPC-NH 2 were used to protect the AuNPs. Therefore, this colorimetric assay, which employs peptides and AuNPs, enables not only a selective but also a simple detection of CatS, visible to the naked eye.

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ACS Applied Nano Materials · 2024 · IF 5.3

3D MoS2/MgIn2S4 Nanoflower Heterojunctions for Photoreduction of Cr(VI): Mechanism, Influence, and Toxicity Evaluation

Xingrui Tong,Jinling Bao,Danfeng Chang,Dapeng Wang,Haibo Chang,Liquan Jing

Designing an efficient hole–electron separation method is essential to improving the photocatalytic efficiency of photocatalysts. Herein, we constructed a 3D MoS2/MgIn2S4 S-scheme heterojunction material using a solvothermal method. The built-in electric field formed by the interaction between MoS2 and MgIn2S4 promoted the separation of electrons and holes, significantly improving the photocatalytic activity of 3D MoS2/MgIn2S4. The 3% MoS2/MgIn2S4 composite photocatalyst successfully achieved a 100% reduction of Cr(VI) within 90 min and demonstrated good hydrogen production efficiency without using a sacrificial agent. Theoretical calculations confirmed the formation of S-scheme heterojunctions. Malondialdehyde and dehydrogenase tests showed that the Cr(VI) solution after reduction was not harmful to plant growth. Furthermore, we systematically investigated the effects of different Cr(VI) concentrations, catalyst dosages, ions, pH values, and organic acids on photocatalytic efficiency. The design of the S-scheme heterojunction photocatalysts provided a promising strategy for the photoreduction of Cr(VI).

研究领域: 环境科学 · 材料科学 · 化学工程
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