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International Journal of Applied Ceramic Technology · 2023 ·Vol. 21 ·期 1 ·319-326 · IF 2.1

Synthesis and electrochemical properties of hydrangea-like (NH4)2V4O9/V5O12·6H2O cathode for zinc-ion battery

Jiajia Song,Lingjiang Kou,Yong Wang,Taotao Ai,Wenhu Li,Koji Kajiyoshi,Panya Wattanapaphawong,Yi Li

Energy density, power density, as well as the cost of aqueous zinc-ion batteries (AZIBs), are largely determined by the cathode material. Among the various cathodic candidates, vanadium-based materials with various oxidation states of vanadium cations and open frameworks have emerged as highly promising options. In this work, a heterogeneous with hydrangea-like (NH 4 ) 2 V 4 O 9 /V 5 O 12 ·6H 2 O as cathode materials for AZIBs. The hydrogen bonds formed by NH 4 + of (NH 4 ) 2 V 4 O 9 , in conjunction with the lattice water in V 5 O 12 ·6H 2 O, sufficiently strengthen the cohesion of the layered structure and expand the interlayer space. As a result, accelerating the diffusion of Zn 2+ ultimately leads to an enhanced overall discharge capacity. Remarkably, the hydrangea-like (NH 4 ) 2 V 4 O 9 /V 5 O 12 ·6H 2 O electrode at a current density of 100 mA g −1 shows a high reversible capacity of 209 mAh g −1 after 150 cycles and higher rate capability (172 mAh g −1 at 500 mA g −1 ). The outstanding electrochemical performance can be attributed to the unique structure of the cathode material and accelerated diffusion coefficient of Zn 2+ .

CAS / MDL: 54010-75-2
研究领域: 材料科学 · 电化学
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ACS Applied Materials & Interfaces · 2021 · IF 9.229

Magnesium Ion Storage Properties in a Layered (NH4)2V6O16·1.5H2O Nanobelt Cathode Material Activated by Lattice Water

Luyao Wei,Ruqian Lian,Dashuai Wang,Yingying Zhao,Di Yang,Hainan Zhao,Yizhan Wang,Gang Chen,Yingjin Wei

Magnesium ion batteries have attracted increasing attention as a promising energy storage device due to the high safety, high volumetric capacity, and low cost of Mg. However, the strong Coulombic interactions between Mg2+ ions and cathode materials seriously hinder the electrochemical performance of the batteries. To seek a promising cathode material for magnesium ion batteries, in this work, (NH4)2V6O16·1.5H2O and water-free (NH4)2V6O16 materials are synthesized by a one-step hydrothermal method. The effects of NH4+ and lattice water on the Mg2+ storage properties in these kinds of layered cathode materials are investigated by experiments and first-principles calculations. Lattice water is demonstrated to be of vital importance for Mg2+ storage, which not only stabilizes the layered structure of (NH4)2V6O16·1.5H2O but also promotes the transport kinetics of Mg2+. Electrochemical experiments of (NH4)2V6O16·1.5H2O show a specific capacity of 100 mA·h·g–1 with an average discharge voltage of 2.16 V vs Mg2+/Mg, highlighting the potential of (NH4)2V6O16·1.5H2O as a high-voltage cathode material for magnesium ion batteries.

研究领域: 储能 · 材料科学 · 电化学 · 无机化学
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DALTON TRANSACTIONS · 2018 ·Vol. 47 ·期 48 ·17486-17492 · IF 4.099

Cation-tuned synthesis of the A2SO4·SbF3 (A = Na+, NH4+, K+, Rb+) family with nonlinear optical properties

Fangfang He,Lei Wang,Cuifang Hu,Jing Zhou,Qian Li,Ling Huang,Daojiang Gao,Jian Bi,Xin Wang,Guohong Zou

Four antimony fluoride sulfates named A2SO4·SbF3 (A = Na+, NH4+, K+, Rb+) have been successfully synthesized using a hydrothermal method by introducing Sb3+ cations with a stereochemically active lone pair in sulfates and subsequently tuning the structure through the second monovalent cations. All of the title compounds are stoichiometrically equivalent materials which share a common structural motif composed of a distorted SO4 tetrahedron and an asymmetric SbF3 polyhedron. However, the macroscopic centricities of these four compounds are significantly influenced by the size and coordination environment of cations; Na2SO4·SbF3 crystallizes in centrosymmetric space groups Cmca and (NH4)2SO4·SbF3 in Pbca, while K2SO4·SbF3 and Rb2SO4·SbF3 crystallizes in noncentrosymmetric space group P212121. Complete characterization including thermal analyses, infrared and UV-vis spectroscopy, and theoretical calculations is also reported. Powder second harmonic generation measurement for noncentrosymmetric K2SO4·SbF3 and Rb2SO4·SbF3 indicated that both of them are type I phase-matchable.

研究领域: 无机化学 · 材料科学 · 非线性光学 · 晶体工程 · 固态化学
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Journal of Applied Spectroscopy · 2014 ·Vol. 81 ·期 5 ·807-811 · IF 0.514

Extraction and Determination of Copper(II) in Seafood Using an Acetone-(NH4)2SO4 Aqueous Two-Phase System

Liu Y.,Fan J.,Ma W.,Fu Ch.

An aqueous two-phase system of acetone and (NH 4 ) 2 SO 4 mixture has been developed for the extractive separation of copper (Cu). The complex formed by Cu(II) and Nuclear Fast Red was found to be extracted into the acetone-rich upper phase, and the absorbance of the complex was determined at 465 nm. Beer’s law was obeyed over the concentration range of ~0.6–3.2 mg/l for Cu(II) with a good linearity. The proposed method has been applied to the separation and determination of Cu(II) in seafood samples with a coefficient of variation less than 2.8%. The recovery obtained was ~96.3–101.7%.

研究领域: 分析化学 · 环境化学 · 食品安全检测
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ENVIRONMENTAL SCIENCE & TECHNOLOGY · 2025 · IF 11.3

Impact of NH4+-N on Organic Micropollutant Removal and Antibiotic Resistance Gene Occurrence during Simulated Riverbank Filtration

Jian Zhao,Qiaojuan Wang,Yangrui Huang,Shangbiao Fang,Gang Liu,Weixiao Qi,Yaohui Bai,Walter van der Meer,Jiuhui Qu,Huijuan Liu

Organic micropollutants (OMPs) facilitate the spread of antibiotic resistance genes (ARGs). Ammonia-oxidizing microorganisms (AOMs) are crucial for OMP degradation during riverbank filtration (RBF) and significantly influenced by NH4+-N concentrations. However, the effect of NH4+-N on OMP removal and ARG occurrence in RBF remains unclear. This study aimed to examine the effects of low (∼0.1 mg/L) and high (∼2.2 mg/L) NH4+-N concentrations on OMP removal, ARG occurrence, and microbial communities. NH4+-N addition had no significant effect on the removal of 108 out of 128 OMPs, suggesting that other factors primarily govern the removal process. Notably, NH4+-N addition enhanced the removal of 20 OMPs by 3–70%, including three quinolones (e.g., flumequine), indicating its promotion of specific OMP removals. This effect may primarily result from NH4+-N enhancing OMP biotransformation through the stimulation of AOMs (particularly AOA and comammox) and heterotrophs (e.g., Bradyrhizobium). Furthermore, NH4+-N addition significantly reduced the abundance of eight ARGs, including quinolone ARGs, likely due to its inhibition of antibiotic-resistant bacteria. Additionally, we hypothesize that NH4+-N alleviates OMP selective pressure on microorganisms by promoting OMP conversion through AOMs. This study enhances the understanding of microbe-mediated OMP removal in the presence of NH4+-N and its impact on ARG occurrence during RBF.

CAS / MDL: 12125-02-9
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Journal of Water Process Engineering · 2025 · IF 6.7

Hydroxyl-regulated ZnFe2O4/UV/PDS synergy for green conversion of NH4+-N: Insights from experiment and theory

Youwei Yang,Jianxing Wang,Yan Gao,Xuekun Tang,Chunying Wang,Xianping Luo

ZnFe 2 O 4 catalysts synthesized via hydrothermal (ZFO-H) and sol-gel (ZFO-S) methods were employed to activate peroxodisulfate (PDS) under UV light for the efficient conversion of low-concentration NH 4 + -N into environmentally benign N 2 , offering a promising solution for advanced wastewater treatment. Characterization revealed that the sol-gel-derived ZFO-S exhibited uniform agglomeration, smooth surfaces, and an 80% reduction in surface hydroxyl density (as indicated by the FTIR peak area at 3320 cm -1 ), outperforming both hydrothermally prepared and commercial ZnFe₂O₄ (ZFO-H and ZFO-M, respectively). This study addresses the critical challenge of ammonia nitrogen removal in wastewater, where conventional methods often struggle with low efficiency or secondary pollution. Mechanistic studies demonstrated that ZnFe 2 O 4 facilitated electron transfer at Zn sites to activate PDS, generating reactive species dominated by singlet oxygen ( 1 O 2 ), which drove NH 4 + -N oxidation. Density functional theory (DFT) calculations further elucidated the reaction pathway, highlighting preferential adsorption of NH 3 at oxygen sites on the ZnFe 2 O 4 (311) surface, followed by sequential dehydrogenation and coupling to form N 2 . Under optimal conditions (pH >9.25, 10 mM PDS, 25°C, 3 h), 97.40% of initial 50 mg/L NH₄ + -N was converted to N₂, with negligible NO 3 − byproduct formation (< 6%), demonstrating high feasibility for practical wastewater remediation. The reduced surface hydroxyl groups and lower work function of ZFO-S enhanced electron transfer, underscoring its superior catalytic activity. This work provides a novel strategy for designing hydroxyl-regulated photocatalysts tailored for wastewater treatment and advances the mechanistic understanding of persulfate-based ammonia nitrogen remediation in engineered water systems.

CAS / MDL: 5949-29-1 7782-61-8
研究领域: 环境科学 · 催化化学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Polypyrrole pre-intercalation engineering-induced NH4+ removal in tunnel ammonium vanadate toward high-performance zinc ion batteries

Yangyang Gong,Pengtao Zhang,Shuang Fan,Minghui Cai,Jiangtao Hu,Zhaoyan Luo,Hongwei Mi,Xiantao Jiang,Qianling Zhang,Xiangzhong Ren

Ammonium vanadate with stable bi-layered structure and superior mass-specific capacity have emerged as competitive cathode materials for aqueous rechargeable zinc-ion batteries (AZIBs). Nevertheless, fragile N H…O bonds and too strong electrostatic interaction by virtue of excessive NH 4 + will lead to sluggish Zn 2+ ion mobility, further largely affects the electro-chemical performance of ammonium vanadate in AZIBs. The present work incorporates polypyrrole (PPy) to partially replace NH 4 + in NH 4 V 4 O 10 (NVO), resulting in the significantly enlarged interlayers (from 10.1 to 11.9 Å), remarkable electronic conductivity, increased oxygen vacancies and reinforced layered structure. The partial removal of NH 4 + will alleviate the irreversible deammoniation to protect the laminate structures from collapse during ion insertion/extraction. The expanded interlayer spacing and the increased oxygen vacancies by the virtue of the introduction of polypyrrole improve the ionic diffusion, enabling exceptional rate performance of NH 4 V 4 O 10 . As expected, the resulting polypyrrole intercalated ammonium vanadate (NVOY) presents a superior discharge capacity of 431.9 mAh g −1 at 0.5 A g −1 and remarkable cycling stability of 219.1 mAh g −1 at 20 A g −1 with 78 % capacity retention after 1500 cycles. The in-situ electrochemical impedance spectroscopy (EIS), in-situ X-ray diffraction (XRD), ex-situ X-ray photoelectron spectroscopy (XPS) and ex-situ high resolution transmission electron microscopy (HR-TEM) analysis investigate a highly reversible intercalation Zn-storage mechanism, and the enhanced the redox kinetics are related to the combined effect of interlayer regulation, high electronic conductivity and oxygen defect engineering by partial substitution NH 4 + of PPy incorporation.

CAS / MDL: 7803-55-6 6153-56-6
研究领域: 材料科学 · 能源技术
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Metabolites · 2022 ·Vol. 12 ·期 5 ·444 · IF 5.581

Differential Metabolic Responses of Lettuce Grown in Soil, Substrate and Hydroponic Cultivation Systems under NH4+/NO3− Application

Muhammad Khalid Hameed,Wajid Umar,Ali Razzaq,Tariq Aziz,Muhammad Aamer Maqsood,Shiwei Wei,Qingliang Niu,Danfeng Huang,Liying Chang

Nitrogen (N) is an essential element for plant growth and development. The application of a balanced and optimal amount of N is required for sustainable plant yield. For this, different N sources and forms are used, that including ammonium (NH4+) and nitrate (NO3−). These are the main sources for N uptake by plants where NH4+/NO3−ratios have a significant effect on the biomass, quality and metabolites composition of lettuce grown in soil, substrate and hydroponic cultivation systems. A limited supply of N resulted in the reduction in the biomass, quality and overall yield of lettuce. Additionally, different types of metabolites were produced with varying concentrations of N sources and can be used as metabolic markers to improve the N use efficiency. To investigate the differential metabolic activity, we planted lettuce with different NH4+/NO3−ratios (100:0, 75:25, 50:50, 25:75 and 0:100%) and a control (no additional N applied) in soil, substrate and hydroponic cultivation systems. The results revealed that the 25% NH4+/75% NO3−ratio increased the relative chlorophyll contents as well as the biomass of lettuce in all cultivation systems. However, lettuce grown in the hydroponic cultivation system showed the best results. The concentration of essential amino acids including alanine, valine, leucine, lysine, proline and serine increased in soil and hydroponically grown lettuce treated with the 25% NH4+/75% NO3−ratio. The taste and quality-related compounds in lettuce showed maximum relative abundance with the 25% NH4+/75% NO3−ratio, except ascorbate (grown in soil) and lactupicrin (grown in substrate), which showed maximum relative abundance in the 50% NH4+/50% NO3−ratio and control treatments, respectively. Moreover, 1-O-caffeoylglucose, 1,3-dicaffeoylquinic acid, aesculetin and quercetin-3-galactoside were increased by the application of the 100% NH4+/0% NO3−ratio in soil-grown lettuce. The 25% NH4+/75% NO3−ratio was more suitable in the hydroponic cultivation system to obtain increased lettuce biomass. The metabolic profiling of lettuce showed different behaviors when applying different NH4+/NO3−ratios. Therefore, the majority of the parameters were largely influenced by the 25% NH4+/75% NO3−ratio, which resulted in the hyper-accumulation of health-promoting compounds in lettuce. In conclusion, the optimal N applications improve the quality of lettuce grown in soil, substrate and hydroponic cultivation systems which ultimately boost the nutritional value of lettuce.Keywords:ammonium;lettuce;metabolites;nitrogen;nitrate

研究领域: 农业 · 植物科学 · 代谢组学
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INORGANIC CHEMISTRY · 2022 · IF 5.436

NH4IO2F2 and (NH4)3(IO2F2)3·H2O: A Series of Ammonium-Containing Fluoroiodates with Wide Band Gaps

Jianlong Huang,Fengjiao Guo,Zhiyong Guo,Jianbang Chen,Bin Dai,Feng Yu

A series of ammonium-containing fluoroiodates, NH4IO2F2 and (NH4)3(IO2F2)3·H2O, with isolated [IO2F2] units have been fabricated by a fluorine-oxygen substitution strategy from NH4IO3. The two compounds crystallize in the orthorhombic system, but in different space groups, noncentrosymmetric Pca21 for NH4IO2F2 and centrosymmetric Pnma for (NH4)3(IO2F2)3·H2O, and show wide band gaps of 4.53 eV for (NH4IO2F2) and 4.55 eV for ((NH4)3(IO2F2)3·H2O). In addition, NH4IO2F2 exhibits a 1.2 × KDP second harmonic generation response, a short ultraviolet cutoff edge in iodates, and a good crystal growth habit. The crystal of NH4IO2F2 with a size of 11 × 5 × 2 mm3 was obtained by the aqueous solution method. The results enrich the structural diversity of iodate and supply a greater understanding of the design of new functional materials based on the fluoroiodates.

研究领域: 无机化学 · 材料科学
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MATERIALS LETTERS · 2023 · IF 3

Incorporation of NH4+ in flower-like zinc phosphate pigment to enhance the corrosion resistance of waterborne epoxy

Yulin Zhang,Xiteng Li,Dongjie Yang,Hu Cai,Ziqi Ma,Yu Zhang,Suihan Cui,Zhongzhen Wu

Herein, the three-dimensional (3D) flower-like pigments of micro-nano scaled zinc phosphate (FZP) and ammonium zinc phosphate (FNZP) were successfully synthesized by hydrothermal synthesis method for improving the corrosion resistance of waterborne epoxy (WEP) coating. The micro-structures, chemical compositions and corrosion resistance of the as-obtained specimens were characterized by SEM, XRD, FT-IR, XPS and EIS, respectively. The results indicated that the 3D flower-like FZP and FNZP pigments were comprised of self-assembled nano-micro sheets with an average thickness of 20 nm ∼ 100 nm. Moreover, the remarkable enhancements of compactness and anticorrosion performance, especially for the FNZP-incorporated coating, were principally contributed to the well dispersibility and favourable solubility, which lengthened the permeation pathway and promoted the formation of passivation film.

研究领域: 材料科学 · 腐蚀与防护
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RARE METALS · 2025 · IF 11

Oxygen Vacancies Modulation of Ammonium Tungsten Bronze by NH4+-Assisted Heat Treatment for Highly Sensitive Detection of NO2

Qiu-Yue Zheng,Xiao-Li Cheng,Jing Tang,Ting-Ting Wang,Xian-Fa Zhang,Li-Hua Huo,Chao-Bo Huang,Zoltán Major,Yong-Sheng Zhang,Peng-Jin Ye,Ying-Ming Xu

en Introducing oxygen vacancies has emerged as an essential strategy to affect the sensing properties of nanomaterials. However, existing methods for manipulating oxygen require high cost, complex operation, and harsh conditions. Herein, a simple NH 4 + -assisted heat treatment approach was designed to regulate the concentration of oxygen vacancies of ammonium tungsten bronze ((NH 4 ) 0.25 WO 3 , named as NWO). The resultant NWO-300 sensor exhibited an extremely high response of 118 to 1 ppm NO 2 at 40°C. It achieved a detection limit as low as 10 ppb. Such outstanding sensing properties of NWO-300 were ascribed to the modulated electronic structure and increased active sites caused by oxygen vacancies. The formation of a large number of oxygen vacancies in NWO-300 is due to the H and N atoms in NH 3 can extract O atoms on the surface of materials, which was confirmed by X-ray photoelectron spectroscopy (XPS) and thermogravimetric-mass spectrometry (TG-MS) techniques. Moreover, the excellent NO 2 detection ability of the NWO-300 sensor enables the detection of air quality under different floors, and its development can be utilized in the field of environmental monitoring applications. 摘要 zh 引入氧空位已成为影响纳米材料传感性能的一项关键策略。然而, 现有调控氧空位的方法成本高昂、操作复杂且条件苛刻。因此, 设计了一种简单的NH 4 + 辅助热处理方法来调节铵钨青铜 ((NH 4 ) 0.25 WO 3 , 命名为NWO) 中氧空位的浓度。制备的NWO-300传感器在40 °C时对1 ppm 的NO 2 显示出高达118的响应, 其检测限低至10 ppb。NWO-300传感器如此出色的传感性能归因于氧空位所导致的电子结构的调节和活性位点的增加。NWO-300中大量氧空位的形成是由于NH 3 中的H和N原子可以从材料表面提取O原子, 这一点通过XPS和TG-MS技术得到了证实。此外, 由于NWO-300传感器出色的NO 2 检测能力使其能够检测不同楼层的空气质量, 其开发可用于环境监测领域。

CAS / MDL: 12333-11-8
研究领域: 材料科学 · 气体传感 · 纳米材料 · 环境监测
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CHINESE JOURNAL OF STRUCTURAL CHEMISTRY · 2023 · IF 2.2

AIO3·H6TeO6 (A = NH4+, Rb+): Two telluric acid and iodate Co-crystalline compounds with second harmonic generation response

Shunye Yu,Yi Shui,Shuo Liu,Gan Huang,Canxiao Huang,Chunhui Geng,Lili Liu,Hongming Liu

Two co-crystalline compounds containing telluric acid and iodate, namely AIO 3 ·H 6 TeO 6 (A ​= ​Rb + , NH 4 + ), were investigated as potential nonlinear optical materials. They crystallize into isostructural and consist of isolated [IO 3 ] group and [H 6 TeO 6 ] molecule linked by hydrogen bonds and charge interactions of Rb + /NH 4 + . They show phase-matching second harmonic generation responses with moderate intensity of 1.2 ​× ​KDP (Rb + ) and 1.1 ​× ​KDP (NH 4 + ). They also possess large optical band gaps over 4.25 ​eV and can be easily grown from aqueous solutions. The local dipole moment calculations based on the structures of AIO 3 ·H 6 TeO 6 (A ​= ​K + , Rb + , NH 4 + ) series of compounds indicate that the change of A + cation in their structural frame causes a slight change in the arrangement directions of [IO 3 ] and [Te(OH) 6 ] groups, and further induces their SHG responses of different intensities at the macroscopic level.

研究领域: 材料科学 · 光学 · 晶体学
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