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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2025 · IF 3.9

Fabrication of MoS2/h-BN Heterojunctions to Tune Interfacial Electronic Properties for Enhanced Oxidative Desulfurization

Yanan Huang,Wenjing Xie,Jia Li,Jixing Liu,Hao Chen

Oxidative desulfurization (ODS) is one of the most promising processes for producing clean fuels to meet the requirements for the clean use of fossil fuels. In this study, a MoS2/h-BN heterojunction was synthesized using the chemical vapor deposition method, leading to a modified electronic structure at the surface. X-ray photoelectron spectroscopy, electron paramagnetic resonance, and electrochemical impedance spectroscopy suggested the occurrence of interfacial electronic reorganization and enhanced charge transfer efficiency due to the formation of a well-defined heterojunction. Hydrogenation temperature-programmed reduction revealed a strong interaction between h-BN and MoS2, which contributed to the highly efficient performance of the heterojunction for ODS applications. As a result, although h-BN showed very low ODS activity, its catalytic activity was enhanced so much and even comparable to that of pure MoS2 after loading with only 1.7 wt % MoS2 on h-BN to construct MoS2/h-BN heterojunctions.

CAS / MDL: 10241-05-1
研究领域: 材料科学 · 催化化学 · 能源化学 · 纳米材料 · 表面科学 · 环境化学
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES · 2025 ·Vol. 26 ·期 18 ·9016 · IF 4.9

Biphasic Adaptations of Gastric Epithelial Cells in Chronic H. pylori Infection from Stress to Tolerance

Xiulin Zhang,Yang He,Xiaolu Zhang,Ziyi Liang,Wendong Wang,Zhenyu Da,Jianyi Lv,Meng Guo,Xueyun Huo,Xin Liu,Jing Lu,Lixue Cao,Xiaoyan Du,Zhongming Ge,Zhenwen Chen,Xuancheng Lu,Jianzhong Zhang,Changlong Li

Helicobacter pylori(H. pylori) is a well-known pathogen associated with chronic gastric infection, progressing from gastritis to gastric adenocarcinoma, but the dynamic phenotypic and molecular characteristics of gastric epithelial cells during sustained infection remain unclear. We established a chronic infection model using the human gastric epithelial cell line GES-1, exposed toH. pylorior its lysate across 30 generations, dynamically assessing cell proliferation, migration, invasion, apoptosis, autophagy, and epithelial–mesenchymal transition (EMT) markers, with RNA sequencing for transcriptomic changes and a Mongolian gerbil model to validate chronic pathological progression. AcuteH. pyloriexposure induced pronounced morphological changes; suppressed proliferation, migration, and invasion; triggered apoptosis; and blocked autophagic flux, while long-term stimulation reversed these effects. EMT markers showed progressive loss of epithelial characteristics with chronic infection. RNA sequencing revealed a dynamic shift from inflammation-driven apoptosis to adaptive survival mechanisms. In vivo, prolonged infection induced dynamic TLR expression alongside progressive gastric pathology, including atrophy and dysplasia. Our study provides new molecular evidence for dynamic cellular and immunological adaptations of gastric epithelial cells under chronicH. pyloriinfection, highlighting critical intervention windows for preventing gastric carcinogenesis.

CAS / MDL: 548-62-9
研究领域: 微生物学 · 胃肠病学 · 分子生物学 · 传染病学 · 癌症研究 · 细胞生物学
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Nano-Micro Letters · 2022 ·Vol. 14 ·期 1 ·1-12 · IF 23.655

Growth of Tellurium Nanobelts on h-BN for p-type Transistors with Ultrahigh Hole Mobility

Yang Peng,Zha Jiajia,Gao Guoyun,Zheng Long,Huang Haoxin,Xia Yunpeng,Xu Songcen,Xiong Tengfei,Zhang Zhuomin,Yang Zhengbao,Chen Ye,Ki Dong-Keun,Liou Juin J.,Liao Wugang,Tan Chaoliang

The growth of high-quality single-crystalline Te nanobelts is reported by introducing atomically flat hexagonal boron nitride (h-BN) nanoflakes into the chemical vapor deposition system as the growth substrate. The field-effect transistor based on Te grown on h-BN exhibits an ultrahigh hole mobility up to 1370 cm 2  V −1  s −1 at room temperature.

研究领域: 材料科学 · 电子工程
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CHEMICAL ENGINEERING SCIENCE · 2025 · IF 4.3

Electron density engineering in Pd/H-TiO2 catalysts for enhanced photocatalytic CO2 to formic acid

Ruijie Ma,Huimin Gao,Jinpeng Zhang,Jieying Jing,Wen-Ying Li

Photocatalytic reduction of CO 2 to formic acid (HCOOH) offers a sustainable pathway for carbon utilization, yet its efficiency is fundamentally limited by poor CO 2 adsorption and rapid electron-hole recombination in conventional photocatalysts. To address this challenge, a series of Pd-loaded hydrogenated TiO 2 catalysts (x wt%Pd/H-TiO 2 ) were developed through a synergistic hydrogen reduction-impregnation strategy, aiming to regulate the electron density of Pd active sites and enhance interfacial charge separation. Systematic characterization revealed that increasing Pd loading (0.6–1.4 wt%) effectively trapped photogenerated electrons, suppressing recombination losses and elevating electron density at Pd sites. Combined with optimized CO 2 adsorption capacity (0.178 mmol·g −1 ) and accelerated charge transfer, the 1.0 wt%Pd/H-TiO 2 catalyst achieved a HCOOH production rate of 14.14 mmol·g cat −1 ·h −1 under mild conditions (30 °C, 2.0 MPa, 4.57 mW·cm −2 ), outperforming most reported TiO 2 -based systems. Mechanistic studies further demonstrated a strong correlation between Pd-induced electronic effects and multi-electron CO 2 activation kinetics. This work provides a scalable catalyst design paradigm for balancing charge dynamics and surface reactivity in photocatalytic CO 2 valorization.

研究领域: 环境催化 · 材料科学 · 能量转换 · 纳米技术 · 物理化学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

Modulation of multiferroic properties of h-YMnO3 due to lattice distortion caused by Yb doping

Yong Zhou,Jiamei Liu,Xudong Zhao,Bin Yang,Bing Li,Xiaoyang Liu

Because of their unique electrical and magnetic properties, the perovskite multiferroic materials exhibit significant potential in spintronic device applications. However, synthesizing room-temperature multiferroic materials with robust magneto-electric coupling effects remains a major challenge. In this work, Yb 3 + , with an ionic radius slightly smaller than Y 3+ , was selected for A -site doping in the h -YMnO 3 , which has a high ferroelectric transition temperature (T C ∼ 900 K) and a low antiferromagnetic transition temperature (T N ≤ 70 K). This similar ionic radius allows Yb to substitute the Y site effectively while introducing distinct electronic states, thereby optimizing the structure and multiferroic properties of h -YMnO 3 without significantly altering the crystal structure. A series of Yb-doped Y 1- x Yb x MnO 3 ( x  = 0, 0.1, 0.2, 0.3, 0.4, 0.5 and 1) materials were synthesized via conventional solid-phase reaction. The effects of Yb doping on the structure, magnetism, and ferroelectricity of h -YMnO 3 were studied. X-ray diffraction (XRD) and corresponding XRD refining results show that as Y 3+ is replaced by Yb 3+ with smaller radii, the cell parameters and cell volume of Y 1- x Yb x MnO 3 decrease, the cell is compressed, and the lattice structure of Y 0.5 Yb 0.5 MnO 3 obtained under the condition of Yb semi-doping changes significantly. Subsequent magnetic and room-temperature ferroelectric test results show that the Y 1- x Yb x MnO 3 series samples have anti-ferromagnetic ground states. In particular, the proper inclination of Mn 3+ ions in the double perovskite structure of Y 0.5 Yb 0.5 MnO 3 generates strong Dzyaloshinskii-Moriya (DM) interactions, resulting in relatively strong antiferromagnetism. The antiferromagnetic Neel temperature (T N ) from 37 K to 41 K. Yb 3+ -induced inclined ferroelectricity enables Y 0.8 Yb 0.2 MnO 3 to achieve the highest ferroelectric polarization of 0.030 µC cm −2 , which is 180 % greater than that of h -YMnO 3 . The results demonstrate that Yb doping plays a crucial role in regulating the structure and multiferroic properties of h -YMnO 3 , offering a novel strategy for developing room-temperature multiferroic materials with robust magneto-electric coupling.

CAS / MDL: 1314-37-0 1317-34-6
研究领域: 材料科学 · 凝聚态物理
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JOURNAL OF CATALYSIS · 2026 · IF 6

Insight into the activation mechanism of methylene C–H bond over Ce–Al composite oxide

Xiangwei Ren,Yue Zhang,Shuzhen Lyu,Li Wang,Ruichen Liu,Guozhu Liu,Rongrong Zhang

Oxidation of methylene compounds remains a critical challenge due to the difficult activation of C–H bond. Herein, Ce–Al composite oxide was prepared and employed for oxidation of 2-alkyl-anthrone and anthracene to corresponding anthraquinone (AQ) which is used widely in the H 2 O 2 production by the anthraquinone process and fine chemical industries, with air at mild conditions. Characterization results show that incorporation of Ce, existing partially in CeAlO 3 phase, results in the generation of oxygen vacancies and enhancement of reducibility. The optimal Ce–Al composite oxide (10%CeAl) exhibits superior performance in oxidation of 2-alkyl-anthrone and anthracene to AQ. The conversion of 100% could be achieved for 2-alkyl-anthrone to AQ at reaction time of 8 h and for 2-alkyl-anthracene to AQ at 15 h over 10%CeAl, with 100% selectivity. In-situ electron paramagnetic resonance measurements and DFT calculations reveal that the Ce–O–Al structure in CeAlO 3 phase promotes the formation of carbon-centered radical R • through altering the C–H cleavage mechanism from hydrogen atom transfer to proton-coupled electron transfer (PCET), and superoxide anion radicals (O 2 •− ) formed on oxygen vacancies promote oxidation of R • .

CAS / MDL: 1306-38-3 7440-31-5
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JOURNAL OF ENVIRONMENTAL MANAGEMENT · 2026 · IF 9.2

Atomic H*-mediated electroreduction process facilitates purifying the industrial wastewater: Insights into mechanisms and detoxication

Jia Yuan,Chunyu Wang,Xinrui Yuan,Xin Wang,Xu Gao,Yuxuan He

Due to the excessive chemical-energy consumption, conventional treatments ( e.g. Fenton or catalytic ozonation) have faced great challenges when treating chemical wastewater containing tetrabromobisphenol S (TBBPS), a prevalent brominated flame retardant. This study proposes an electrocatalytic active atomic hydrogen (H*)-mediated electroreduction strategy, enabling enhanced degradation of TBBPS into intermediates with lower toxicity and higher biodegradability. A palladium-modified electrocatalytic microfiltration membrane (EMM) was developed to efficiently generate H*, which played a dominant role in the reductive debromination of TBBPS. By conducting quenching experiments, it was found that free H* and adsorbed H* co-dominate the TBBPS removal process. Under optimized conditions, the EMM achieved nearly complete removal (∼100%) of TBBPS (100 mg L −1 ) within 60 min, with a low energy consumption of 9.53 kWh/m 3 . The degradation pathway of TBBPS was proposed on the results of calculations and LC-MS analysis, and the evidence demonstrated the lower toxicity of the degradation intermediates. These findings emphasize the prospects of H*-mediated electroreduction strategy as a green and environmentally friendly treatment for industrial wastewater treatment.

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JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY · 2018 ·Vol. 18 ·期 5 ·3291-3298 · IF 1.354

Enhanced Thermal Conductivity of Polyimide Composites Filled with Modified h-BN and Nanodiamond Hybrid Filler

Yang Xi,Yu Xiaoyan,Naito Kimiyoshi,Ding Huili,Qu Xiongwei,Zhang Qingxin

A new thermally conductive and electrically insulative polyimide were prepared by filling different amounts of hexagonal boron nitride (h-BN) particles, and the thermal conductivity of Polyimide (PI) composites were improved with the increasing h-BN content. Based on this, two methods were applied to improve thermal conductivity furtherly at limited filler loading in this paper. One is modifying the h-BN to improve interface interaction, another is fabricating a nano-micro hybrid filler with 2-D h-BN and 0-D nano-scale nanodiamond (ND) to build more effective conductive network. Both surface modification and hybrid system have a positive effect on thermal conductivity. The composites introducing 40 wt% hybrid filler (the weight ratio of ND/modified BN was 1/10) showed the highest thermal conductivity, being up to 0.98 W/(m K) (5.2 times that of PI). In addition, the composites exhibits excellent electrical insulation, thermal stability properties etc.

研究领域: 材料科学 · 聚合物复合材料 · 热管理材料
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JOURNAL OF ORGANOMETALLIC CHEMISTRY · 2021 · IF 2.369

Palladium catalyzed selective amination of B(7)-H for synthesis of o-carborane fused isoquinolinones

Ke Cao,Ji Wu,Cai-Yan Zhang,Li-Fang Ding,Junxiao Yang

A palladium catalyzed intramolecular amination of B(7)-H for synthesis of o -carborane fused isoquinolinones has been developed. Kinds of o -carborane fused isoquinolinones decorated with active groups have been synthesized with good to excellent yields. A plausible mechanism involving palladium catalyzed electrophilic B-H activation/amination was proposed.

研究领域: 有机化学 · 催化化学 · 硼化学 · 药物化学
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COMPOSITES COMMUNICATIONS · 2026 · IF 7.7

Bioinspired honeycomb structure enables high thermal conductivity in h-BN/PSAE composites via TBA-templating

Yujie Yang,Huixing Lin,Jiaqi Li,Yang Gao,Xiaogang Yao,Haiyi Peng

Efficient thermal management is a critical challenge for next-generation electronics, where conventional polymer-based materials suffer from inherently low thermal conductivity. Inspired by natural honeycomb structures, we developed a freeze-casting strategy to fabricate high-performance hexagonal boron nitride (h-BN)/polysilylaryl-enyne (PSAE) composites exhibiting enhanced thermal conductivity. By leveraging the unidirectional crystallization of tert-butyl alcohol (TBA), a highly ordered h-BN honeycomb scaffold was constructed, facilitating the formation of efficient phonon conduction pathways. The composites, with a low h-BN (10 μm) ratio of 23 vol%, exhibit an outstanding omni-directional thermal conductivity of 4.71 W/(m·K) along the z-axis and 3.44 W/(m·K) along the x-axis, significantly outperforming conventional polymer composites. Moreover, dielectric characterization confirms that the honeycomb structure enhances anisotropic dielectric behavior ( ε rz  = 3.68, ε rx  = 3.32, for h-BN (10 μm) at 23 vol%). The proposed bioinspired approach presents a scalable and effective route for developing lightweight, thermally conductive composites for advanced electronic applications.

CAS / MDL: 75-65-0 75-78-5
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TURKISH JOURNAL OF CHEMISTRY · 2026 ·Vol. 50 ·期 3 ·285-299 · IF 2

[H]-mediated enhancement of the Fenton reaction over a Pd/UiO-66(Zr)-F4 catalyst

LI JUANHONG,WANG SUQIN,LIU XIN,LIU FENG

A [H]-accelerated catalytic Fenton system was developed using Pd/UiO-66(Zr)-F4 as the catalyst. This system enabled the regeneration of Fe²⁺ and facilitated the continuous generation of both ·OH and 1O2 through [H]-mediated electron transfer at ambient temperature and pressure. Under the conditions of 0.2 g L−1 catalyst (Pd loading 0.516 wt%), 25 μM Fe2+, 60 mL min−1 H2 flow (as the [H] source), 20 mM H2O2, and pH 3, approximately 89% of carbamazepine (initial concentration 20 mg L−1) was degraded within 3 h using trace iron. However, the catalytic activity of Pd/UiO-66(Zr)-F4 gradually declined from 89% to 53% over six reaction cycles. This decrease was likely due to loss of specific surface area caused by microstructural degradation associated with hydrogen spillover effects.

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Marine Drugs · 2015 ·Vol. 13 ·期 6 ·3360-3367 · IF 2.853

Myrothecols G and H, Two New Analogues of the Marine-Derived Quinone Sesquiterpene Penicilliumin A

Ying Fu,Ping Wu,Jinghua Xue,Hanxiang Li,Xiaoyi Wei

Two new quinone sesquiterpenes named myrothecols G and H (1and2), a pair of C-1′ diastereomers of 13-hydroxyl penicilliumin A, were isolated from the mycelia solid cultures ofMyrotheciumsp. SC0265. Their structures, including the absolute configurations, were established on the basis of the spectroscopic data combining with the theoretical conformational analysis. The cytotoxic activities of1and2were tested against a panel of human tumor cell lines.

研究领域: 天然产物化学 · 药物化学 · 肿瘤药理学 · 结构生物学 · 微生物学
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