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FUEL PROCESSING TECHNOLOGY · 2022 · IF 8.129

Fabrication of Z-scheme CdS/H5PMo10V2O40/g-C3N4 for the photocatalytic depolymerization of lignin into aromatic monomers

Mingyu Cui,Chong Liang,Wei Zhao,Xutang Liu,Linyang Dong,Dingkai Wang,Shuiyuan Fu,Zhijie Jiang,Fei Wang,Xianyong Wei

As the most abundant resource composed of aromatic groups in nature, lignin harbors significant potential for the production of bio-based fuels and chemicals. In recent years, solar-driven photocatalysis with its mild, low cost and environmental benign, has been employed for lignin depolymerization . Herein, we designed a Z -scheme CdS/H 5 PMo 10 V 2 O 40 /g-C 3 N 4 (CdS/HPA-2/CN) photocatalyst via hydrothermal method for the photocatalytic depolymerization of lignin. The prepared CdS/HPA-2/CN presents a nanoflower-like morphology with the average diameter of ∼600 nm. With the presence of electron-mediated HPA-2, CdS/HPA-2/CN exhibits the enhanced separation and transfer capacity of photogenerated charge carriers through Z -scheme mechanism. Result shows that the total yield ( Y ) of vanillin and vanillic acid from lignin depolymerization over optimized CdS/HPA-2/CN can reach to 32.7 mg/g lignin in DMF/formic acid ( v / v  = 40/10) for 4 h. Reusability experiment of optimized CdS/HPA-2/CN displays that Y (26.5 mg/g lignin) can still reach to 81.0% of initial one after three cycles. Qualitative analysis of depolymerized products reveals that most components are aromatic compounds with the dominant products of vanillin and vanillic acid. Evidence also shows that photocatalysis promotes the reaction and small molecular products increased significantly after depolymerization. In addition, mechanism experiments and electron spin resonance tests exhibit that h + , ·O 2 − and ·OH took part in lignin depolymerization together and the effect sequence was ·O 2 −  > ·OH >  h + . In this work, as an electron mediator, HPA-2 provides the inspiration for construction of Z -scheme heterojunction , and CdS/HPA-2/CN exhibits enormous potential in lignin depolymerization by photocatalysis.

研究领域: 材料科学 · 环境科学 · 催化化学
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Selective degradation of organic pollutants by highly dispersed Fe, Ni anchored on nitrogen carbon activating persulfate system: Electron transfer promotion, the impact of pollutant redox and adsorption properties

Yuqi Liu,Yongqing Zhang,Lijin Zhang,Waseem Hayat,Xuefeng Wu,Hong Meng,Que Wu

The advanced oxidation processes using persulfate (PS-AOPs) as oxidant is an effective way to remove refractory organic pollutants from environment. Designing activators with higher activation efficiency and stability plays an important role in degradation of organic pollutants via PS-AOPs. Furthermore, redox and adsorption properties of pollutants also affect the selective degradation efficiency. In this study, we synthesized FeNi@CN derived from ZIF-8 in which highly dispersed Fe and Ni were anchored on nitrogen (N) doped carbon (C). The activator exhibited high activation potential and stability for paracetamol (PCT) degradation by activated peroxymonosulfate (PMS). The FeNi@CN/PMS system degraded PCT through electron transfer pathway, and the coordination of Fe-N and Ni-N improved the efficiency of catalyst mediated electron transfer. The abundant pyridinic N provided a large number of sites for PMS complexation. The bimetallic synergistic effect and N doping endowed the excellent comprehensive performance of FeNi@CN. The significant impact of pollutant redox and adsorption properties on degradation efficiency were also studied. It was observed that high half-wave potential ( E 1/2 ) and excessive adsorption were not conducive to electron transfer. Multi-parameter linear fitting was performed on the degradation rates of different pollutants using half-wave potential and pseudo first order adsorption rate constants, which showed the good correlation among them. This work not only provided insights into the mechanism and the influence of activator structure on electron transfer in PMS activation, but also proposed a new model to describe the effects of redox and adsorption properties on selective degradation of various category pollutants.

研究领域: 环境科学 · 化学工程
✓ 已验证 DOI 高影响因子
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NEW JOURNAL OF CHEMISTRY · 2019 ·Vol. 43 ·期 36 ·14327-14335 · IF 3.069

Ligase chain reaction-based electrochemical biosensor for the ultrasensitive and specific detection of single nucleotide polymorphisms

Wancun Zhang,Fang Hu,Xianwei Zhang,Wei Meng,Yaodong Zhang,Yinsen Song,Huanmin Wang,Peng Wang,Yueqing Gu

In this study, a simple, robust, label-free electrochemical biosensor based on the ligase chain reaction (LCR) was developed for the highly sensitive and selective detection of single nucleotide polymorphisms (SNPs) using Fe(CN)63−/Fe(CN)64− as a redox indicator. High sensitivity and specificity were achieved by using the LCR, which employs a thermostable and single-base discerning Hifi Taq DNA ligase to repeatedly ligate adjacently hybridized LCR-specific probes during thermal cycles, resulting in the highly specific exponential amplification of DNA targets. The electrochemical signal of the biosensor was further decreased using stem-loop probe DNA (SL-DNA), which specifically hybridized with LCR products on the electrodes. The linear dynamic range and high sensitivity of the mutant DNA (MutDNA) and wild-type DNA (WtDNA) LCR-based electrochemical biosensors for the detection of MutDNA and WtDNA were studied in vitro, with a broad linear dynamic range of 10 aM to 10 pM and detection limits of 1.18 aM and 0.35 aM, respectively. In addition, the MutDNA and WtDNA LCR-based electrochemical biosensors were able to accurately detect allele frequency changes as low as 0.1%. In summary, the developed LCR-based electrochemical biosensor provides a useful platform to monitor SNPs in a highly sensitive and specific manner.

研究领域: 生物传感 · 分子生物学 · 电化学 · 遗传分析
✓ 已验证 DOI 高影响因子
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ELECTROANALYSIS · 2025 ·Vol. 37 ·期 9 ·e70046 · IF 2.3

Sensitive Detection of Hesperidin Based on CN-MWCNTs/Ti3C2 Composite Modified Electrode

Wei Liu,Yanhua Sun,Songfeng Yin,Hao Li,Miao Yang,Pingping Huang,Zi Li,Nannan Wang,Deming Li

In this study, carbon nitride-multiwalled carbon nanotubes/ MXenes (CN-MWCNTs/Ti 3 C 2 ) nanocomposites with excellent properties were synthesized by a convenient method and characterized using various methods. By modifying the CN-MWCNTs/Ti 3 C 2 composites on glassy carbon electrode, an electrochemical sensor capable of sensitive and rapid detection of hesperidin (HPD) was established. Under the optimal conditions, the sensor showed excellent detection performance for HPD (0.1 M PBS (pH 7.0)). The linear range was 0.05–503 μM, and the detection limit (S/N = 3) was 0.017 μM. In addition, the sensor has the advantages of good immunity to interference, stability and reproducibility.

CAS / MDL: 10236-47-2
研究领域: 分析化学 · 纳米生物技术 · 电化学传感 · 药物分析 · 天然产物检测
✓ 已验证 产品关联 DOI 高影响因子
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RSC Advances · 2014 ·Vol. 4 ·期 81 ·42991-42995 · IF 3.708

Fe4[Fe(CN)6]3: a cathode material for sodium-ion batteries

He Sun,Haobo Sun,Wei Wang,Handong Jiao,Shuqiang Jiao

Insoluble Prussian blue (IPB), Fe4[Fe(CN)6]3, is synthesized at room temperature and found to achieve a relatively high storage capacity of 146 mA h g−1 (at a 20 mA g−1 rate) as the cathode material for Na-ion batteries with high potential plateaus. XRD, SEM and TEM are employed to characterize the morphology and microstructure of the as-synthesized IPB. First-principles calculation is introduced to study the electrochemical mechanism. Generally, the environmental friendliness and low cost of the material make it possible to be used for large-scale electric storage applications.

CAS / MDL: 7705-08-0 14434-22-1
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STAR Protocols · 2023 · IF 0

Protocol for ambient CO2 capture and conversion into HCOOH and NH4H2PO4

Shuchao Jiang,Jikai Sun,Guoqing Ren,Weiqiao Deng

Summary CO 2 capture and utilization into liquid fuels and high-added-value chemicals has been regarded as an attractive strategy to mitigate excessive carbon emissions. Here, we present a protocol to capture and convert CO 2 into pure formic acid (HCOOH) solution and solid fertilizer (NH 4 H 2 PO 4 ). We describe steps for synthesis of an IRMOF3-derived carbon-supported PdAu heterogeneous catalyst (PdAu/CN-NH 2 ), which can efficiently catalyze (NH 4 ) 2 CO 3 -captured CO 2 into formate under ambient conditions. For complete details on the use and execution of this protocol, please refer to Jiang et al. (2023). 1

研究领域: 环境科学 · 化学工程
✓ 已验证 DOI PubMed
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Nanoscale Advances · 2023 ·Vol. 5 ·期 20 ·5661-5670 · IF 4.7

A Prussian blue analog as a decorporation agent for the simultaneous removal of cesium and reactive oxygen species

Tingyu Xue,Fang Liu,Bin Lu,Qingrong Dong,Bin Zhao,Tianqing Chen,Kun Zhang,Jianguo Li,Jiangfeng Du

Radioactive cesium (Cs) is a significant concern due to its role as a major byproduct of nuclear fission and its potential for radioactive contamination. Internal contamination with radioactive Cs is characterized by immoderate production of reactive oxygen species (ROS), resulting in severe radiation damage. Therefore, the development of therapeutic strategies should focus on enhancing the excretion of radioactive Cs and reducing radiation-induced oxidative damage. However, current therapeutic drugs like Prussian blue (PB) have limited efficacy in addressing these issues. In this study, we present Cu3[Fe(CN)6]2 (CuFe) nanoparticles, a Prussian blue analog (PBA), which can not only efficiently sequester Cs but also exhibit resistance against radiation damage. The results of the adsorption studies demonstrate that CuFe outperforms PB in terms of adsorption performance. Further mechanistic investigations indicate that the increased adsorption capacity of CuFe may be attributed to the presence of additional defects resulting from the [Fe(CN)6] missing linkers. Moreover, CuFe mimics the functions of catalase (CAT) and superoxide dismutase (SOD) by effectively eliminating O2˙− and H2O2 while scavenging ˙OH, thereby mitigating ROS induced by radiative Cs. Importantly, in vivo study confirms the efficient Cs decorporation capability of CuFe. The fecal cumulative excretion rate of CuFe reaches 69.5%, which is 1.45 times higher than that of PB (48.8%). These findings demonstrate that CuFe exhibits excellent Cs removal performance and ROS scavenging ability, making it an attractive candidate for the treatment of Cs contamination.

研究领域: 药理学 · 放射医学 · 纳米医学
✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

A co-doped oxygen reduction catalyst with FeCu promotes the stability of microbial fuel cells

Han Li,HuiHui Shi,Yi Dai,HengHui You,Samuel Raj Babu Arulmani,Hongguo Zhang,Chunhua Feng,Lei Huang,Tianyu Zeng,Jia Yan,Xianjie Liu

Air cathode microbial fuel cell (AC-MFC) cannot be used on a large scale because of its low oxygen reduction reaction (ORR) efficiency. Despite the fact that bimetallic catalysts can greatly enhance the oxygen reduction rate by regulating the electronic structure of the active site, the flaws of insufficient exposure of the active site and easy metal agglomeration limit its catalytic activity. Herein, we report on the preparation of a stable heteroatomic substrate using a copper material organic framework as a precursor, covered by Fe-based active sites. As a result of dipole-dipole interactions, the reduced product Fe 2+ forms a weak Fe-O surface that is conducive to the adsorption of active substances. The presence of Fe 0 enhances the electrical conductivity of the catalytic, thus promoting ORR efficiency. Through redox coupling, the D-band center of Fe at FeCu@CN is optimized and brought close to the Fermi level to facilitate electron transfer. Notably, FeCu@CN demonstrates a superior power density of 2796.23 ± 278.58 mW m −3 , far exceeding that of Pt/C (1363.93 ± 102.56 mW m −3 ), in the application of microbial fuel cells (MFCs). Meanwhile, the MFC-loaded FeCu@CN maintains excellent stability and outstanding output voltage after 1000 h, which provides feasibility for large-scale application.

研究领域: 环境科学 · 材料科学 · 能源科学
✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2017 · IF 3.133

Enhanced sodium ion storage performance of Na3V2(PO4)3 with N-doped carbon by folic acid as carbon-nitrogen source

Hui Xiao,Xiaobing Huang,Yurong Ren,Haiyan Wang,Jianning Ding,Shibiao Zhou,Xiang Ding,Yuandao Chen

Na 3 V 2 (PO 4 ) 3 /nitrogen doped carbon (NVP/CN) composites have been fabricated by a simple and low cost solid-state technique using folic acid as the carbon-nitrogen source. The structure, morphology and electrochemical performance of NVP/CN composites coated with various carbon-nitrogen layer contents are well investigated. The results reveal that the NVP/CN composite with 3.3 wt% carbon-nitrogen exhibits the largest specific surface area, with a uniform carbon-nitrogen layer thickness of approximately 2 nm. When tested as cathode material for sodium ion battery , NVP/CN composite with 3.3 wt% carbon-nitrogen displays an outstanding high rate properties with the discharge capacity of 95 and 91 mAh g −1 at 10 and 20 C, respectively, and long cycle life up to 3000 times even at a high rate of 10 C due to the smallest charge-transfer resistance and highest Na + diffusion coefficient . The results suggest that folic acid is a promising carbon-nitrogen source for construction of NVP/CN and other cathode materials.

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
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RSC Advances · 2020 ·Vol. 10 ·期 30 ·17653-17659 · IF 3.119

Enhancing the performance of LARP-synthesized CsPbBr3 nanocrystal LEDs by employing a dual hole injection layer

Dingyan Xu,Qun Wan,Siyao Wu,Yu Zhao,Xinglei Xu,Liang Li,Gufeng He

Lead halide perovskites have been considered promising materials for optoelectronic applications owing to their superior properties. CsPbBr3 nanocrystals (NCs) with a narrow particle size distribution and a narrow emission spectrum are synthesized by ligand-assisted re-precipitation (LARP), a low-cost and facile process. In inverted CsPbBr3 NC LEDs, a dual hole injection layer (HIL) of 1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile (HAT-CN)/MoO3 is introduced to enhance hole injection and transport, because HAT-CN can extract electrons easily from the hole transport layer and leave a large number of holes there. The current and power efficiencies of the optimized device with a dual HIL are 1.5- and 1.8-fold higher than those of the single HIL device. It is believed that the dual HAT-CN/MoO3 HIL effectively promotes hole injection and has promise for application in many other devices.

研究领域: 材料科学 · 光电技术
✓ 已验证 DOI 高影响因子
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ACS Sensors · 2025 · IF 9.1

Co3[Co(CN)6]2-Mediated Olfactory and Visual Dual-Modality Ammonia Sensing

Xinhua Zhao,Xiaxia Xing,Zhenxu Li,Yi Zhang,Zhu Zhang,Tingting Wang,Dachi Yang

In the emerging ammonia (NH3) economy, both olfactory and visual sensing are desired for leakage detection, in which olfactory sensing enables a fast response and wide detection range, while visual sensing ensures high selectivity. However, little is reported on the sensing material as a mediator to synergistically combine the dual-modality NH3 sensing. Here, Co3[Co(CN)6]2 microcubes (Co–CN MCBs) mediators have been developed for olfactory and visual dual-modality NH3 sensing. In olfactory sensing, porous chitosan-decorated Co3O4/Co3[Co(CN)6]2 microcages (CS@Co–O/Co–CN MCGs) have been obtained via [Co(CN)6]3–-governed self-assembly, glycerol-assisted reduction, and Kirkendall effect-driven hollowing. Beneficially, MCGs exhibit a 1 s fast response (500 ppm) and a 0.5–10,000 ppm wide detection range at room temperature. In visual sensing, colorimetric sensing paper (CSP) incorporated with anthocyanin, Co–CN, and poly(vinyl alcohol) has been achieved, which presents 10–320 ppm visual NH3 detection through a pink-to-brown transition. Further, highly selective NH3 sensing has been acquired through machine learning-powered classification of MCGs’ response and CSP’s specific NH3 chromogenic behavior. Notably, combining dual-modality sensing has achieved desired NH3 detection due to the boosted NH3 adsorption on Co–CN MCBs’ active sites and the synergistic effect of their-mediated heterostructures. Practically, our dual-modality sensing device has been integrated to detect NH3 with reliable responses.

CAS / MDL: 9002-89-5
研究领域: 材料科学 · 传感器与传感技术 · 环境监测 · 纳米材料 · 气体检测 · 机器学习应用
✓ 已验证 产品关联 DOI PubMed 高影响因子
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Materials Today Energy · 2018 · IF 0

Direct implementation of K3Fe(CN)6 as cathode materials of sodium-ion batteries

De Gao,Rui Du,Chenggang Zhou,Bo Han,Kaisheng Xia,Qiang Gao,Jinping Wu

Transition metal cyanides are considered as a promising cathode candidate of sodium-ion batteries. Herein, we reported a direct implementation of commercial K 3 Fe(CN) 6 (KFC) as active cathode material of SIBs by a simple recrystallization method. Our results suggest that by integrating conductive carbons (SuperP, abbreviated as SP) and multi-walled carbon nanotubes (CNTs) with KFC, an efficient conducting network could be well established for the utilization of KFC active components, thereby endows excellent cyclic and rate performances. Specifically, the KFC/SP/CNTs composite delivers its theoretical capacity of 81 mAh g −1 at 0.1C, and a reversible capacity of 75.6 mAh g −1 at 1C which maintains 62.6 mAh g −1 after 500 cycles. At ultrahigh rate of 12C, the capacity retention can reach 68% of initial. Our effort suggests that direct implementing industrial KFC as cathode materials for SIBs is highly feasible, which may provide a low-cost cathode candidate of sodium-ion batteries for large-scale energy storage.

研究领域: 材料科学 · 电化学
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