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JOURNAL OF HAZARDOUS MATERIALS · 2017 · IF 6.065

In-situ synthesis of 3D GA on titanium wire as a binder- free electrode for electro-Fenton removing of EDTA-Ni

Shulong Wen,Zhuyu Niu,Zhen Zhang,Lianghao Li,Yuancai Chen

Ethylenediaminetetraacetic acid (EDTA) could form stable complexes with toxic metals such as nickel due to its strong chelation. The three-dimensional (3D) macroporous graphene aerogels (GA), which was in-situ assembled by reduced graphene oxide (rGO) sheets on titanium wire as binder-free electrode, was presented as cathode for the degradation of EDTA-Ni in Electro-Fenton process. The X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), Transmission Electron Microscope (TEM) and Brunauer-Emmett-Teller (BET) results indicated 3D GA formed three dimensional architecture with large and homogenous macropore structure and surface area. Cyclic Voltammetry (CV), Linear Sweep Voltammetry (LSV) and Rotating Ring-disk Electrode (RRDE) results showed that the 3D GA cathode at pH 3 displayed the highest current density and electrochemical active surface area (ECSA), and better two-electron selectivity for ORR than other pH value, confirming the 3D-GA cathode at pH 3 has the highest electrocatalytic activity and generates more H 2 O 2 . The factors such as pH, applied current density, concentration of Fe 2+ , Na 2 SO 4, and aeration rates of air were also investigated. Under the optimum conditions, 73.5% of EDTA-Ni was degraded after reaction for 2   h. Mechanism analysis indicated that the production of OH on the 3D GA cathode played an important role in the removal of EDTA-Ni in the 3D GA-EF process, where the direct regeneration of Fe 2+ on the cathode would greatly reduce the consumption of H 2 O 2 . Therefore, it is of great promise for 3D-GA catalyst to be developed as highly efficient, cost-effective and durable cathode for the removal of EDTA-Ni.

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Materials · 2025 ·Vol. 18 ·期 2 ·393 · IF 3.2

Construction and Properties of Wood-Based Tannin–Iron-Complexed Photothermal Material Populus tomentosa Carr.@Fe-GA for Solar Seawater Desalination System

Hongyan Zhu,Xinyu Li,Shijie Li,Ximing Wang,Yabo Ma,Jin Zhang,Yunpeng Ren,Jianguo Zhao

Desalinating seawater is a crucial method for addressing the shortage of freshwater resources. High-efficiency, low-cost, and environmentally friendly desalination technologies are key issues that urgently need to be addressed. This work usedPopulus tomentosa Carr.as a matrix material and preparedPopulus tomentosa Carr.@Fe-GA through a complexation reaction to enhance the water evaporation rate and photothermal conversion efficiency of seawater desalination. The concentration of the impregnation solution was further refined, and the bonding mechanism along with the thermal stability of the composite photothermal material was investigated, including an assessment of their photothermal conversion efficiency. The research results indicate that the evaporation rate of water in a 3.5% NaCl solution forPopulus tomentosa Carr.@Fe-GA under light intensity conditions of one sun reached 1.72 kg·m−2·h−1, which was an increase of 44.5% compared to untreatedPopulus tomentosa Carr.It achieved a photothermal conversion efficiency of 95.1%, an improvement of 53.6% over untreatedPopulus tomentosa Carr., and maintained stability and high evaporation performance (95.4%) even after prolonged rinsing. This work realizes the functional utilization of seawater desalination withPopulus tomentosa Carr.and offers a novel approach for the development and use of wood-derived photothermal material.

CAS / MDL: 1401-55-4
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ENVIRONMENTAL RESEARCH · 2025 · IF 7.7

Enhanced PMS activation efficiency and SMX degradation performance via Fe(II)/Fe(III) cycling with efficient CCF@MoS2@GA-Fe catalyst

Dawei Gao,Haixiang Wang,Qiaoli Lu,Chao Ye,Jingsheng Cai,Lili Wang

Antibiotics, widely used to treat bacterial infections and as agricultural feed additives, pose significant environmental threats due to their persistence, particularly sulfamethoxazole (SMX), which is frequently detected in various ecosystems. Traditional wastewater treatment methods are often ineffective in their removal. This study presents a cost-effective three-dimensional CCF@MoS 2 @GA-Fe (CMGF) catalyst, with cotton fabric as a support to enhance peroxymonosulfate (PMS) activation in advanced oxidation processes (AOPs). Findings indicates that Mo(IV) active sites in CMGF significantly enhanced electron transfer and redox cycling of Fe(II)/Fe(III), ensuring sustained PMS activation and achieving approximately 3.8 times higher degradation efficiency compared to non-catalytic processes. After five cycles, CMGF retains its high catalytic activity. Key active species during PMS activation include singlet oxygen ( 1 O 2 ), hydroxyl radicals (•OH), and sulfate radicals (SO 4 − •). This research elucidates the catalytic mechanisms and degradation pathways of the CMGF/PMS system, highlighting its potential for removing organic pollutants from water.

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SENSORS AND ACTUATORS B-CHEMICAL · 2024 · IF 8

Ga-doped carbon quantum dot-sensitized luminol molecularly imprinted electrochemiluminescence sensor used for the efficient detection of cypermethrin in aquatic products

Jinjie You,Rui Chen,Qiaofen Pan,Zeming Zhang,Aili Sun,Rongrong Zhang,Hua Liu,Xizhi Shi

The development of new electrochemical sensitizing materials is crucial for rapid detection technology. In this study, gallium-doped carbon quantum dots (Ga@CQDs) were synthesized using a one-pot hydrothermal approach to serve as coreactant for luminol. A molecular-imprinted electroluminescence sensor was prepared for rapid, sensitive cypermethrin (CYP) detection using in-situ electrodeposition. Ga doping reduces CQDs' band gap, boosts conductivity and catalysis, and enhances luminol's ECL signal. The advancement in molecular imprinting technology significantly enhances the sensor's ability to selectively detect CYP, while also providing robust interference resistance. The ECL intensity of the sensor correlated linearly with CYP concentration (0.05–100 μM) under optimal conditions (R 2 = 0.9912, LOD= 0.03 μM). In practical applications, recovery rates of water and aquatic product samples ranged from 86.4 % to 98.0 %, with RSD that did not exceed 8.13 %. A Ga@CQDs-based luminol sensitizing system for molecularly imprinted electrochemical sensors provides a solution for fast, sensitive CYP detection in environmental and aquatic products.

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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Ga-Ni modified MCM-41@HZSM-5 core-shell zeolite for catalytic fast pyrolysis of wheat straw to produce monocyclic aromatics

Hong Tian,Huimin Mao,Jiawei Wang,Yi Cheng

The HZSM-5 zeolite was modified through alkali treatment (NaOH) and metal loading (Ga, Ni), followed by constructing an MCM-41 layer to create a core–shell molecular sieve catalyst. With the feedstock of wheat straw, this work investigated the effects of various catalysts on pyrolysis product distribution and bio-oil composition with a tubular furnace and Py-GC/MS. The results showed that with the alkali-treated HZSM-5, the yield of monocyclic aromatic hydrocarbons (MAHs) in the bio-oil reached 40.35%, with an overall bio-oil yield of 21.16%. Metal-modified zeolites, exhibiting enhanced acidity, further optimized the bio-oil composition, producing an MAH yield of 61.48% and 27.31% bio-oil yield. Bimetal loading with Ga and Ni further enhanced MAH selectivity, delivering an MAH yield of 69.48% and a bio-oil yield of 27.79%. The synergy between Ga and Ni suppressed excessive aromatization and polymerization into polycyclic aromatic hydrocarbons (PAHs), favouring MAH formation. Constructing an MCM-41 layer further promotes the selectivity of MAHs. Compared to uncoated catalysts, those coated with MCM-41 significantly improved monocyclic aromatic yields, achieving the highest MAH yield of 83.61%.

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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Efficient and inexpensive preparation of mesoporous silica microspheres and their highly selective adsorption-cycling performance for Ga(III) in acidic solutions

Yu She,Lin Shao,Min Yi,Yong Fang,Linqiao Qin,Yu Liu,Xinpeng Wang,Kaituo Wang

In this paper, efficient, economical and environmentally friendly mesoporous silica microspheres (MSMs) were prepared for the first time by reversed-phase suspension-dispersion method using water glass and acetic acid as raw materials. MSMs had excellent sphericity, with particle size concentrated at 100 µm, specific surface area of 207.90 m 2 /g and pore volume of 0.47 cm 3 /g. Adsorption equilibrium of Ga(III) by MSMs was reached in 30 min on 30 ppm GaCl 3 with dosage of 2 g/L and pH = 3, conforming to the pseudo-second-order kinetic model. The adsorption isotherm showed that the adsorption of Ga(III) by MSMs is endothermic process with saturation adsorption of 83.47 mg/g at 328 K. The K d of MSMs for Ga(III) was above 8000 in three multivariate systems of zinc ore leaching residues, fly ash and e-waste, showing excellent selectivity. The desorption equilibrium of 78.44 % was reached at 2 mol/L H 2 SO 4 for 120 min, and the adsorption rate of Ga(III) on MSMs was still exceeded 90 % after five adsorption–desorption cycles, showing that MSMs have excellent cycling performance. The fixed-bed column experiments showed the efficient separation and enrichment performance of MSMs for Ga(III) in simulated leachate. The adsorption process in MSMs is synergistic interaction is between physical adsorption and ion-exchange, with ion-exchange being the main mechanism. This provides a new approach to address the issues of poor adsorption capacity and slow adsorption–desorption rate faced by adsorbents for the highly selective recover of Ga(III) from zinc ore leaching residues, fly ash and e-waste, which is potentially promising for application.

CAS / MDL: 13450-90-3
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FUEL · 2025 · IF 7.5

Enhancing the efficiency of methylcyclohexane dehydrogenation of Pt/Al2O3 catalyst doped by Ga and Ce adding: Unraveling the role of oxygen vacancy

Chen-Xu Chen,Jing-Pei Cao,Nai-Yu Yao,Wen Tang,Wei Jiang,Chuang Zhang,Xiao-Yan Zhao,Xiao-Yu Qiao,Tungalagtamir Bold

Improving the catalytic efficiency and catalyst life of Pt/Al 2 O 3 catalyst for methylcyclohexane dehydrogenation is of great significance for the study of organic liquid hydrogen storage. In this work, the promotion effects of Ga and Ce on the substantial improvement of catalytic stability and activity over the Pt / Al 2 O 3 during the methylcyclohexane dehydrogenation were investigated. The catalyst with optimizing Ga and Ce loading (1.5 wt%) exhibits ∼99.76 % selectivity and H 2 evolution rate of 2102 mol/g Pt /min at 300 °C. In 100 h long-time reaction, the conversion of methylcyclohexane remains around 75 % with no significant decrease. The characterization results show that introducing proper amount of Ga and Ce helps Ga 3+ cations incorporate into the lattice structure of CeO 2 that increase concentration of oxygen vacancies and CeO 2 reducibility in the catalyst, which boost the capability of methylcyclohexane dehydrogenation and tolerance for coke formation. Thus, the excellent stability and activity are achieved over the GaCe-modified catalyst. This study may share new light on the rational construction of highly efficient Pt-based catalysts for methylcyclohexane dehydrogenation.

研究领域: 催化化学 · 能源材料 · 表面科学 · 纳米催化 · 氢储能 · 材料化学
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Journal of Materials Chemistry B · 2021 ·Vol. 9 ·期 23 ·4735-4745 · IF 6.331

A 3D printed Ga containing scaffold with both anti-infection and bone homeostasis-regulating properties for the treatment of infected bone defects

Minqi Wang,Yiqi Yang,Guanghao Chi,Kai Yuan,Feng Zhou,Liang Dong,Haibei Liu,Qinghui Zhou,Weihua Gong,Shengbing Yang,Tingting Tang

Large bone defects face a high risk of infection, which can also lead to bone homeostasis disorders. This seriously hinders the bone healing process; therefore, the help of a dual-functional scaffold that has both anti-infection and bone-homeostasis-regulating capacities is needed in the treatment of infected bone defects. In this study, a 3D printed dual-functional scaffold composed of poly-ε-caprolactone (PCL), mesoporous bioactive glasses (MBG), and gallium (Ga) was produced. In vitro experiments demonstrated the excellent antibacterial ability of the PCL/MBG/Ga scaffold against methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli (E. coli). The scaffold also significantly inhibited osteoclastic activity and promoted osteogenic differentiation. Furthermore, a rabbit model with an infected bone defect in the radius was used to evaluate the in vivo bone healing capability of PCL/MBG/Ga. The results demonstrate that the PCL/MBG/Ga scaffold can significantly accelerate bone healing and prevent bone resorption, suggesting its potential for application in repairing infected bone defects.

研究领域: 生物材料学 · 骨科医学 · 再生医学
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APPLIED SURFACE SCIENCE · 2026 · IF 6.9

Tuning product selectivity in dimethyl oxalate hydrogenation via Ga-promoted Cu/SiO2 catalysts: the interplay between Cu+/Cu0 sites and surface acidity

Xiaofang Wen,Hongcan Lou,Zheng Li,Jiehao Xie,Zirui Qin,Xingkun Chen,Yuan Tan,Nian Lei,Wei Lu,Yunjie Ding

The development of efficient catalysts for the selective hydrogenation of dimethyl oxalate (DMO) to high-value oxygenates is of great industrial importance. This study presents a systematic investigation into the promotional effect of gallium (Ga) on Cu/SiO 2 catalysts for tailoring product selectivity in DMO hydrogenation. A series of Ga x Cu 30 /SiO 2 catalysts with varying Ga loadings (x = 0.5, 1, 3 wt%) were synthesized via the ammonia evaporation method. With a moderate Ga doping of 0.5 wt%, the Ga 0.5 Cu 30 /SiO 2 catalyst achieved an exceptional ethylene glycol (EG) yield of 74 %, which is three times higher than its Ga-free counterpart (23 %). Further increases in Ga loading to 1 and 3 wt% redirected the reaction pathway, steering the selectivity towards ethanol (ET, 81 %) and 2-methoxyethanol (MT, 54 %), respectively. Characterization by N 2 O titration, XRD, XPS, in situ FT-IR and H 2 -TPR revealed that Ga incorporation fine-tunes the synergy between metallic Cu 0 (for H 2 dissociation) and Cu + sites (for C=O bond polarization). Concurrently, the generated surface acid sites facilitate subsequent dehydration and hydrogenolysis steps. Consequently, the catalytic performance is directly correlated with the evolution of Cu valence states and surface acidity. This work provides a rational strategy for designing multifunctional catalysts for the selective synthesis of target chemicals from DMO.

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ACS Applied Electronic Materials · 2023 · IF 4.7

3D “House of Cards” Structured Composites of Zn/Ga Layered Double Hydroxide/Molybdenum Disulfide with Potential Application for Impedance Respiratory Frequency Sensor

Qingyue Xu,Wenjing Li,Qi Qi,Ying Guo

Respiration is an important physiological signal that can be used to monitor human health and activity. This study presents a high-performance inorganic composite-based humidity sensor for respiration monitoring. The sensor is composed of a 3D nanostructure of ZnGa-layered double hydroxide (ZnGa-LDH) growing in situ on negatively charged MoS2 wafers, obtained by co-precipitation. By adjusting the MoS2 content, the resulting ZnGa-LDH/MoS2 composite displays a 3D “house of cards” structure with a larger surface area than pure ZnGa LDH or MoS2. The sensor exhibits nearly 3 orders of magnitude impedance change from the humidity range of 11% to 95% RH, fast response/recovery time of 1.5/5 s, hysteresis difference of 2.93%, and long-term stability and high repeatability. The optimized humidity sensor can distinguish between different breathing patterns, as well as the breathing rate/depth of the subject. The conductive mechanism of the material has also been analyzed by combining with the complex impedance curve of the material. This study not only provides an easy approach to adjust the hydrophilic/hydrophobic surface of the materials to control the humidity sensing ability but also develops a humidity sensor that can reflect the breathing conditions of the human body, potentially having applications in respiratory monitoring.

CAS / MDL: 10196-18-6
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2023 ·Vol. 30 ·期 15 ·43702-43713 · IF 5.8

Construction of Z-scheme Ti/Ga co-doped ZnO heterostructure photocatalyst with graphitic carbon nitride for efficient visible-light-driven dye degradation

Guo Jin,Sun Yihua,Luo Qiuzi,Zhang Jiangyu,Fang Liang

Innovative solar-driven heterostructure photocatalysts are promising for removing the organic contaminants in the water environment. In this work, a sequence of well-defined Z-scheme Ti-Ga co-doped ZnO/g-C 3 N 4 (TGZ/CN) heterostructure photocatalysts were developed via a simple sol–gel method and the single-phase dispersion method in order to realize the cooperative improvement from the Ti/Ga co-doping and construction of heterostructure. The synthesized samples were analyzed by a variety of characterization techniques, and the photocatalytic activity was assessed by photodegradation of methylene blue (MB) under visible light irradiation. Compared to the ZnO and g-C 3 N 4 , the TGZ/CN composite demonstrated higher photocatalytic performance for the degradation of MB indicating an efficient photocatalytic degradation rate of 95.4% in 105 min under visible light. Moreover, the TGZ/CN photocatalyst exhibited excellent stability after five cycles of MB photodegradation. Furthermore, the as-prepared composites’ possible photocatalytic mechanism was discussed in detail. The improved photocatalytic performance primarily resulted from the effectively reduced band gap of ZnO after Ti/Ga co-doping and the facilitated separation of photoexcited e − /h + pairs caused by the construction of Z-scheme heterojunction. This work offers novel insights in developing hybrids with highly efficient photocatalytic activity towards future environmental applications. Graphical abstract

CAS / MDL: 69365-72-6 5970-45-6
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CERAMICS INTERNATIONAL · 2023 · IF 5.2

Exploring the photoelectrocatalytic performance of spinel- and delafossite-like CuMM’O4 (M, M’ = Al, Ga, In) obtained from pseudobinary CuMO2-based solid solution

Bao-Feng Shan,Zhong Yang,Zong-Yan Zhao,Jin Zhang,Qing-Ju Liu

In this study, the focus revolves around the synthesis, characterization, and subsequent evaluation of CuMM’O 4 (M, M’ = Al, Ga, In) photoelectrocatalysts, notable for their distinct spinel- and delafossite-like structures. These novel materials are derived from a pseudobinary CuMO 2 -based solid solution. Specifically, the delafossite-like CuAlInO 4 and CuGaInO 4 manifest a trigonal superstructure within the R 3 ‾ m R3‾m space group, defined by structural motifs comprising [InO 6 ] octahedra, [CuO 5 ] hexahedra, and [AlO 5 ] or [GaO 5 ] hexahedra. This study spans a comprehensive analysis encompassing optical properties, electrical characteristics, electronic structure, and the ensuing photoelectrochemical performancer. This exploration integrates experimental analyses and density functional theory calculations to discern the intricacies of these materials. The assessed CuMM’O 4 samples display favorable optical traits and band-edge positions conducive to facilitating visible-light-driven photoelectrochemical water-splitting. Among the evaluated samples, the delafossite-like CuGaInO 4 photocathode stands out due to its notably elevated carrier density and reduced resistance for carrier transport, distinguishing it from CuAlGaO 4 and CuAlInO 4 . Consequently, it exhibits superior photoelectrochemical activity. CuGaInO 4 , serving as an unadorned photocathode, demonstrates a noteworthy photocurrent density of 8.6 μA/cm 2 under 0.61V RHE and 102.05 μA/cm 2 at 0.15 V RHE . Moreover, it achieves a peak incident photon-to-current efficiency of approximately 1.86 % at 0.61 V RHE under a 480 nm wavelength.

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