APPLIED SURFACE SCIENCE
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2023
·
IF 6.7
Gengzhe Shen,Jing Kong,Yuqing Fei,Lin Xu,Liuyan Zhang,Xiaohua Jie,De Ning,Zhengjian Chen
In this work, layered double hydroxide (LDH) and reduced graphene oxide (rGO) were incorporated into Zn/Ni matrix coating by cold-spraying on the surface of Mg alloys. Inside the resulting GLG@Zn/Ni coating, LDH/rGO are homogeneously dispersed and inner-connected to a protective network. Compared with other coatings without LDH or rGO nanosheets, the GLG@Zn/Ni coating shows the best corrosion resistance, with a high self-corrosion potential at − 1.174 V (vs. − 1.471 V for Mg), a decent self-corrosion current density of 344.7 μA·cm −2 (vs. 878.3 μA·cm −2 for Mg), and the longest available protection (>720 h) against corrosion. Electrochemical and morphological characterizations reveal a synergistic effect of the coating compositions in enhancing corrosion resistance. In detail, the LDH/rGO network inside the coating restricts the penetration of the corrosive medium, particularly for LDH, which has the capacity to capture corrosive Cl − ions. Meanwhile, Ni promotes the conversion of Zn into passivation layers, which then spread to fill the corrosion pores and interphase cracks. This transformation ultimately leads the GLG@Zn/Ni coating to become a unified whole, providing excellent corrosion resistance.
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高影响因子
CHEMOSPHERE
·
2023
·
IF 8.8
Hai Liang,Wanting Wang,Haiyan Liu,Xinzhong Deng,Dan Zhang,Yuxuan Zou,Xuehua Ruan
Engineering magnesium oxide (MgO)-modified biochar (MgO-biochar) with high porosity and active MgO load is a feasible pathway to enhance phosphate adsorption capacity. However, the blockage to pores caused by MgO particles is ubiquitous during the preparation, which seriously impaired the enhancement in adsorption performance. In this research, with the intent to enhance phosphate adsorption, an in-situ activation method based on Mg(NO 3 ) 2 -activated pyrolysis technology was developed to fabricate MgO-biochar adsorbents with abundant fine pores and active sites simultaneously. The SEM image revealed that the tailor-made adsorbent has well-developed porous structure and abundant fluffy MgO active sites. Its maximum phosphate adsorption capacity was coming up to 1809 mg/g. The phosphate adsorption isotherms are in accordance well with the Langmuir model. The kinetic data, which agreed with the pseudo-second-order model, indicated that chemical interaction is existing between phosphate and MgO active sites. This work verified that the phosphate adsorption mechanism on MgO-biochar was composed of protonation, electrostatic attraction, monodentate complexation and bidentate complexation. In general, the facile in-situ activation method using Mg(NO 3 ) 2 pyrolysis illuminated biochar activation with fine pores and highly efficient adsorption sites for efficient wastewater treatment .
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PubMed
高影响因子
Catalysts
·
2018
·Vol. 8
·期 8
·296
·
IF 3.465
Shuqi Fang,Kang Bi,Qiao Zhang,Lingpeng Chen,Yongming Sun,Hongyu Huang,Longlong Ma,Chenguang Wang
Layered double hydroxide (LDH) is a layered solid containing positively charged layers with negatively charged anions as an interchangeable interlayer. In this research, Mg(Al)O supports were synthesized with three different Mg:Al molar ratios, and bimetallic PtSn catalysts were loaded onto the supports via the anion exchange method. The properties of ethane dehydrogenation of the PtSn/Mg(Al)O catalysts were investigated. The results show that the structure and properties of the PtSn/Mg(Al)O catalysts were influenced by the Mg:Al molar ratio of the hydrotalcites, which consequently influenced the ethane dehydrogenation performance. When the Mg:Al ratio was 5:1, the ethane dehydrogenation performance was optimal, relative to the Mg:Al ratios of 2:1 and 10:1.Keywords:hydrotalcite;Mg:Al molar ratio;anion exchange method;ethane dehydrogenation
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高影响因子
CERAMICS INTERNATIONAL
·
2024
·
IF 5.1
Jianjian Wang,Yue Yu,Zhiqiang Li,Hualin Wang,Shimin Liu,Tingting Yao,Weiwei Jiang,Nan Wang,Chaoqian Liu,Wanyu Ding,Zhihua Zhang,Chuang Dong
Multi-component high entropy oxides (HEOs) have attracted enormous attention due to their unique structures and potential applications. The conventional selection strategy to obtain HEOs is to search for equimolar cationic systems to maximize configurational entropy and avoid phase separation. We previously explored non-equimolar cationic rocksalt structure Mg–Co–Ni–Cu–Zn–O HEOs using cluster-plus-glue-atom model. In this paper, the mixing entropy, enthalpy and Gibbs free energy of constructed superclusters were numerically calculated and compared with the correlated crystal structure based on recent studies. It indicated the Gibbs free energy rather than mixing entropy agrees well with the phase stability of HEOs. Mg 28 Co 17 Ni 19 Cu 16 Zn 16 O 96 shows the optimal phase stability which is related to the lowest Gibbs free energy, reflecting a regular octahedral environment preferred by the cation composition in the system. Enthalpy and entropy are among important design criteria in determining the phase stability of HEOs but the function of enthalpy is obviously higher than that of entropy. This study provides a comprehensive way to access HEOs which is undoubtedly very important for the development of other non-equimolar cationic high entropy materials such as carbides , silicides , borides or nitrides .
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高影响因子
JOURNAL OF MATERIALS RESEARCH
·
2015
·Vol. 30
·期 10
·1639-1647
·
IF 1.647
Xueming Liu,Chunge Niu,Xinping Zhen,Jide Wang,Xintai Su
A phase transfer method was developed to prepare Mg(OH)2 nanosheets and a subsequent adsorption–calcination process was followed to obtain lamellar MgO nanostructures. The as-prepared MgO nanosheets also showed a superior adsorption property of Congo red. Transmission electron microscopy and x-ray diffractometer results indicated that the as-obtained Mg(OH)2 was plate-shaped with a hexagonal crystal structure where MgO possessed a lamellar structure with a cubic phase. The maximum adsorption capacities of Mg(OH)2 and MgO were reached up to 1820 and 2650 mg g−1, respectively. The high adsorption capacity might be related to the particle geometry and large surface area (87.97 m2 g−1 for Mg(OH)2 and 132.31 m2 g−1 for MgO). The adsorbents can be easily regenerated for five times without any significant loss in their adsorption property. The adsorption behaviors of the Mg(OH)2 and MgO adsorbents showed that the adsorption kinetics and isotherms were in good agreement with pseudo-second-order rate equation and Freundlich adsorption model.
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高影响因子
ACS Applied Materials & Interfaces
·
2016
·
IF 7.145
Jing Liu,Bo Zheng,Pei Wang,Xingang Wang,Bin Zhang,Qiuping Shi,Tingfei Xi,Ming Chen,Shaokang Guan
Bioabsorbable magnesium alloys are becoming prominent as temporary functional implants, as they avoid the risks generated by permanent metallic implants such as persistent inflammation and late restenosis. Nevertheless, the overfast corrosion of Mg alloys under physiological conditions hinders their wider application as medical implant materials. Here we investigate a simple one-step process to introduce a cross-linked 3-amino-propyltrimethoxysilane (APTES) silane physical barrier layer on the surface of Mg–Zn–Y–Nd alloys prior to electrostatic spraying with rapamycin-eluting poly(lactic-co-glycolic acid) (PLGA) layer. Surface microstructure was characterized by scanning electron microscope and Fourier transform infrared spectroscopy. Nanoscratch test verified the superior adhesion strength of PLGA coating in the group pretreated with APTES. Electrochemical tests combined with long-term immersion results suggested that the preferable in vitro anticorrosion behavior could be achieved by dense APTES barrier. Cell morphology and proliferation data demonstrated that APTES pretreated group resulted in remarkably preferable compatibility for both human umbilical vein endothelial cells and vascular smooth muscle cells. On the basis of excellent in vitro mechenical property, the animal study on the APTES pretreated Mg–Zn–Y–Nd stent implanted into porcine coronary arteries confirmed benign tissue compatibility as well as re-endothelialization without thrombogenesis or in-stent restenosis at six-month followup.
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PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Yu Yang,Meng Du,Jiaxin Liang,Qian Xu,Wei Liu,Ang Li
The flow-through electroactive membrane adsorption method has been proved to be a promising strategy to enrich low-concentration phosphate. However, the challenges of selective adsorption of phosphate and poor regeneration restrict its industrial application. Here, this study proposed a novel bimetallic Mg-UiO-66@rGO electrode material through the introduction of Mg(II) into UiO-66, which possessed remarkable adsorption selectivity and optimal reproducibility among the reported electrode materials. The maximum phosphate adsorption capacity of Mg-UiO-66(13)@rGO (Zr/Mg = 3:1) was 62.81 mg⋅g −1 at 3.2 V. Furthermore, it maintained the excellent adsorption properties in the presence of all competitive anions and after 30 times of continuous adsorption–desorption. In actual wastewater, Mg-UiO-66(13)@rGO still represented excellent adsorption kinetics of 0.51 mg⋅(g⋅min) −1 and equilibrium adsorption capacity of 61.2 mg⋅g −1 . The superior selectivity of Mg-UiO-66@rGO was attributed to the establishment of coordinative unsaturated metal sites (CUMSs), thus increasing the adsorption sites. The synergic effect of electric field facilitates the breaking and formation of coordination bonds between charged ions and deeper binding sites, boosting the adsorption–desorption ability. Notably, the structural stability is also a key factor in promoting repeated material regeneration. This study advances electrode material to a new level by introducing CUMSs and bimetallic synergies.
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SEMICONDUCTOR SCIENCE AND TECHNOLOGY
·
2025
·Vol. 40
·期 3
·035006
·
IF 2.1
Xingyu Zhang,Lingling Wang,Yawei Wang,Xiangyang Zhao,Rong Fang,Rui Guo,Yue Zhou,Xintong Zhang,Yichun Liu
Modifying the back contact interface plays a key role in improving the efficiency of Cu2ZnSn(S,Se)4 (CZTSSe) solar cells. Aiming at the phase decomposition and carrier recombination issues in the CZTSSe/Mo back contact interface, an ultra-thin Mg(OH)2 intermediate layer was introduced between the Mo substrate and the CZTSSe absorber layer. The Mg(OH)2 intermediate layer effectively suppressed the interface phase decomposition reactions and inhibited the generation of interface secondary phases. Meanwhile, during the high-temperature selenization process, the Mg2+ doped into CZTSSe at the back contact interface, reducing the defects and band offset at the CZTSSe/Mo interface. The performance of the device was improved, with a significant increase in efficiency compared to the control device. This work highlights the modification effect of Mg(OH)2 for improving back contact and also provides an easy-handling method to achieve high-performance CZTSSe solar cells.
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高影响因子
CHEMOSPHERE
·
2024
·
IF 8.1
Yingchao Li,Shujia Wang,Xiao Fang Ouyang,Zhi Dang,Hua Yin
The simultaneous removal of anionic and cationic heavy metals presents a challenge for adsorbents. In this study, acetate (Ac-) was utilized as the intercalating anion for layered double hydroxide (LDH) to prepare a novel biochar composite adsorbent (Ac-LB) designed for the adsorption of Pb(II), Cu(II), and As(V). By utilizing Ac- as the intercalating anion, the interlayer space of the LDH was enlarged from 0.803 nm to 0.869 nm, exposing more adsorption sites for the LDH and enhancing the affinity for heavy metals. The results of the adsorption experiments showed that the adsorption effect of Ac-LB on heavy metals was significantly improved compared to the original FeMg-LDH modified biochar composites (LB), and the maximum adsorption capacity of Pb(II), Cu(II), and As(V) were 402.70, 68.50, and 21.68 mg/g, respectively. Wastewater simulation tests further confirmed the promising application of Ac-LB for heavy metal adsorption. The analysis of the adsorption mechanism revealed that surface complexation, electrostatic adsorption, and chemical deposition were the main mechanisms of action between heavy metals (Pb(II) and Cu(II)) and Ac-LB. Additionally, Cu(II) ions underwent a homogeneous substitution reaction with Ac-LB. The adsorption process of As(V) by Ac-LB mainly relied on complexation and ion-exchange reactions. Lastly, the modification of the LDH structure by Ac − as an intercalating anion, thereby increasing the affinity for heavy metals, was further illustrated using density-functional theory (DFT) calculations.
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高影响因子
POLYMER
·
2024
·
IF 4.1
Xiaoyu Luo,Xiangjun Li,Miaomiao Li,Donghai Ding,Libo Tong
Two-dimensional (2D) nanocomposite coatings and superhydrophobic coatings are applied to retarding corrosion of Magnesium (Mg) and its alloys. However, stability of the delicate micro/nanostructure and corrosion durability are still intractable issues. In this work, a bi-layer superhydrophobic coating with excellent corrosion resistance has been successfully constructed on Mg alloy via a facile spray/spin assisted self-assembly technique. The polyurethane (PU) coating containing well-dispersed hydroxylated hexagonal boron nitride (OH-BN) nanoparticles acts as the barrier layer and “adhesive”, while the superhydrophobic modified h-BN (f-BN) nanoparticles serve as the water-repellent surface. In addition, the modifying agents containing dynamic disulfide bonds provide covalent bonding effect to construct a stable superhydrophobic surface. Hence, the obtained coating presents extreme non-wettability with an impressive static water contact angle (WCA) of 155° as well as possesses outstanding anti-water adhesion, anti-fouling and self-cleaning performance. Meanwhile, the designed coating shows excellent corrosion durability, which the value of |Z| f = 0.01 Hz retains at 9.5 × 10 9 Ω cm 2 , higher than PU coating of two orders of magnitude. The developed coating shows promising potentials as a durable protective material for Mg alloy and other metals and alloys, shedding new lights on developing high-performance corrosion resistance technologies.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Miao Cheng,Junjie Liu,Xiaomian Wang,Yabing Li,Wentao Xia,Qianqian Liu,Jing Hu,Tao Wei,Yun Ling,Bo Liu,Wanfei Li
Rechargeable magnesium-ion batteries (MIBs) are considered to be promising electrochemical energy storage systems because of their low-cost and high safety features. However, the absence of suitable anodes severely impeded the development of high-performance MIBs. Herein, a unique Bi nanospheres homogenously anchored in cellulose nanocrystal (CNC) derived carbon aerogel (CNC-CA@Bi-NS) hybrid, was for the first time fabricated as anode for MIBs through ion-induced gelation and in-situ thermal reduction processes. The successfully incorporation of near-monodisperse Bi nanospheres (4–9 nm diameter) into the interconnected CA matrix could effectively alleviate the volume changes during magnesiation/de-magnesiation alloying reaction, as well as prevent the agglomeration and pulverization of Bi nanospheres. Meanwhile, the N -doped porous matrix not only served as a highly electronic conductive framework but also provided enough space and large surface area for electrolyte storage and penetration, which would facilitate the charge transfer kinetics process. Attractively, the CNC-CA@Bi-NS electrode delivered a remarkable reversible specific capacity of 346 mAh/g at 0.5C (90 % of theoretical capacity) after 100cycles. Furthermore, the CNC-CA@Bi-NS exhibited an excellent rate performance and unprecedented long-term cycling stability with a high coulombic efficiency of ∼ 100 % at 2.0C after 5000cycles. This work provided a new strategy to design and synthesize high-performance Bi-based anode for advanced next-generation MIBs.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Wen Wang,Chuyuan Lin,Fenqiang Luo,Renpin Liu,Xiaochuan Chen,Wangyang Wu,Shiting Wei,Fuyu Xiao,Peixun Xiong,Qinghua Chen,Qingrong Qian,Lingxing Zeng
Hybrid magnesium-lithium batteries (MLIBs) are a promising battery system with safety and exceptional reaction kinetics due to the combination of the dendritic-free deposition Mg metal anode and the rapid Li intercalation cathode. The large interchain frame of VO 2 may contribute to the metal-ion diffusion, making it a suitable cathode for MLIBs. However, the development of VO 2 cathodes for MLIBs is restricted by bad structural stability and low electronic conductivity. Herein, MoS 2 with a hexagonal crystal structure is introduced into the tetragonal VO 2 to construct heterostructure interfaces and induce abundant oxygen vacancies (VO 2 /MoS 2 -2), which enhances the structural stability and reaction kinetics. For this reason, the VO 2 /MoS 2 -2 cathode delivers a remarkable capacity (518 mAh g -1 ) and a considerable cycling lifespan (202 mAh g -1 at 1.0 A g -1 over 700 cycles). Even at low temperatures (-15 and -40 °C), VO 2 /MoS 2 -2 delivers 145 and 115 mAh g -1 after 200 and 50 cycles at 0.1 A g -1 , respectively. This strategy of combinatorial design offers a widely applicable method for the cryogenic resistance and cycling durability of magnesium-lithium batteries.
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