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A Co3O4/graphdiyne heterointerface for efficient ammonia production from nitrates 从硝酸盐中高效生产氨的 Co3O4/graphdiyne 异质界面
IF 5.7 3区 材料科学 Q2 Materials Science Pub Date : 2024-02-01 DOI: 10.1016/S1872-5805(24)60834-6
Zhao-yang Chen, Shu-ya Zhao, Xiao-yu Luan, Zhi-qiang Zheng, Jia-yu Yan, Yu-rui Xue

The nitrate reduction reaction (NtRR) has been demonstrated to be a promising way for obtaining ammonia (NH3) by converting NO3 to NH3. Here we report the controlled synthesis of cobalt tetroxide/graphdiyne heterostructured nanowires (Co3O4/GDY NWs) by a simple two-step process including the synthesis of Co3O4 NWs and the following growth of GDY using hexaethynylbenzene as the precursor at 110 °C for 10 h. Detailed scanning electron microscopy, high resolution transmission electron microscopy, X-ray photoelectron spectroscopy, and Raman characterization confirmed the synthesis of a Co3O4/GDY heterointerface with the formation of sp-C―Co bonds at the interface and incomplete charge transfer between GDY and Co, which provide a continuous supply of electrons for the catalytic reaction and ensure a rapid NtRR. Because of these advantages, Co3O4/GDY NWs had an excellent NtRR performance with a high NH3 yield rate (YNH3) of 0.78 mmol h−1 cm−2 and a Faraday efficiency (FE) of 92.45% at −1.05 V (vs. RHE). This work provides a general approach for synthesizing heterostructures that can drive high-performance ammonia production from wastewater under ambient conditions.

硝酸盐还原反应(NtRR)已被证明是通过将 NO3- 转化为 NH3 来获得氨(NH3)的一种可行方法。在此,我们报告了四氧化三钴/石墨炔异质结构纳米线(Co3O4/GDY NWs)的可控合成方法,该方法采用简单的两步法,包括合成 Co3O4 NWs 和以六乙炔苯为前驱体在 110 ℃ 下 10 小时生长 GDY。详细的扫描电子显微镜、高分辨率透射电子显微镜、X 射线光电子能谱和拉曼表征证实了 Co3O4/GDY 异质界面的合成,界面上形成了 sp-C-Co 键,GDY 和 Co 之间的电荷转移不完全,这为催化反应提供了持续的电子供应,并确保了快速的 NtRR。由于这些优点,Co3O4/GDY NWs 具有优异的 NtRR 性能,其 NH3 产率(YNH3)高达 0.78 mmol h-1 cm-2,在 -1.05 V(相对于 RHE)电压下的法拉第效率(FE)为 92.45%。这项研究为合成异质结构提供了一种通用方法,这种异质结构可在环境条件下推动从废水中产生高性能氨。
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引用次数: 0
Mott-Schottky heterojunction formation between Co and MoSe2 on carbon nanotubes for superior hydrogen evolution 碳纳米管上的钴和 MoSe2 之间形成的莫特-肖特基异质结实现卓越的氢气进化
IF 5.7 3区 材料科学 Q2 Materials Science Pub Date : 2023-12-01 DOI: 10.1016/S1872-5805(23)60782-6
Xian-pei Ren , Qi-wei Hu , Fang Ling , Fei Wu , Qiang Li , Liu-qing Pang

Molybdenum selenide (MoSe2) has been regarded as an advanced electrocatalyst for the hydrogen evolution reaction (HER). However, its electrocatalytic performance is far inferior to platinum (Pt). Combining semiconductors with metals to construct Mott-Schottky heterojunctions has been considered as an effective method to enhance HER activity. In this work, we report a typical Mott-Schottky heterojunction composed of metal Co and semiconductor MoSe2 on carbon nanotubes (Co/MoSe2@CNT), prepared by a sol-gel process followed by thermal reduction. The characterization and theoretical calculations show that a Co/MoSe2 Mott-Schottky heterojunction can cause electron redistribution at the interface and form a built-in electric field, which not only optimizes the free energy of hydrogen atom adsorption, but also improves the charge transfer efficiency during hydrogen evolution. Thus, the Co/MoSe2@CNT has excellent catalytic activity with a low overpotential of 185 mV at 10 mA cm−2 and a small Tafel slope of 69 mV dec−1. This work provides a new strategy for constructing Co/MoSe2 Mott-Schottky heterojunctions and highlights the Mott-Schottky effect, which may inspire the future development of more attractive Mott-Schottky electrocatalysts for H2 production.

硒化钼(MoSe2)一直被认为是一种先进的氢进化反应(HER)电催化剂。然而,它的电催化性能远不如铂(Pt)。将半导体与金属结合起来构建莫特-肖特基异质结被认为是提高氢进化反应活性的有效方法。在这项工作中,我们报告了一种典型的莫特-肖特基异质结,它由碳纳米管上的金属 Co 和半导体 MoSe2(Co/MoSe2@CNT)组成,采用溶胶-凝胶工艺制备,然后进行热还原。表征和理论计算表明,Co/MoSe2 Mott-Schottky 异质结能使电子在界面上重新分布并形成内置电场,这不仅优化了氢原子吸附的自由能,还提高了氢演化过程中的电荷转移效率。因此,Co/MoSe2@CNT 具有优异的催化活性,在 10 mA cm-2 时过电位低至 185 mV,塔菲尔斜率小至 69 mV dec-1。这项工作为构建 Co/MoSe2 Mott-Schottky 异质结提供了一种新策略,并突出了 Mott-Schottky 效应,这可能会启发未来开发更具吸引力的 Mott-Schottky 电催化剂来生产 H2。
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引用次数: 0
Research progress on biomass carbon as the cathode of a metal-air battery 生物质碳作为金属空气电池阴极的研究进展
IF 5.7 3区 材料科学 Q2 Materials Science Pub Date : 2023-12-01 DOI: 10.1016/S1872-5805(23)60784-X
Li-lai Lu, Qing-shan Li, Yuan-na Sun, Kun-bin Kuang, Zhi Li, Tao Wang, Ying Gao, Jun-bo Wang

Metal-air batteries have received significant attention as highly efficient energy conversion and storage devices. Nevertheless, several difficulties, such as the sluggish reaction kinetics of the cathode and the high cost of precious metals, have significantly hampered their commercialization. Biomass carbon materials have emerged as an important alternative for the development of high-performance cathode materials in metal-air batteries, owing to their remarkable electrochemical characteristics, environmental friendliness and cost effectiveness. In recent years, there has been huge progress in the preparation and design of biomass carbon materials. This review summarizes the most recent research on these materials, and the effects of the reaction mechanism, synthesis method and multidimensional (1D, 2D, 3D) structure on their electrocatalytic performance are reviewed. Finally, problems associated with their use and possible new developments are discussed. The review presents new perspectives on the structure of these materials, and provides a basis for the development of efficient, affordable, and stable cathode materials for metal-air batteries.

金属空气电池作为一种高效的能量转换和储存设备受到了广泛关注。然而,阴极反应动力学迟缓和贵金属成本高昂等困难极大地阻碍了其商业化。生物质碳材料因其显著的电化学特性、环境友好性和成本效益,已成为开发金属空气电池高性能阴极材料的重要替代材料。近年来,生物质碳材料的制备和设计取得了巨大进展。本综述总结了有关这些材料的最新研究,并综述了反应机理、合成方法和多维(一维、二维、三维)结构对其电催化性能的影响。最后,还讨论了与这些材料的使用相关的问题以及可能的新发展。综述为这些材料的结构提供了新的视角,为开发高效、经济、稳定的金属空气电池阴极材料奠定了基础。
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引用次数: 0
A 2D montmorillonite-carbon nanotube interconnected porous network that prevents polysulfide shuttling 可防止多硫化物穿梭的二维蒙脱石-碳纳米管互连多孔网络
IF 5.7 3区 材料科学 Q2 Materials Science Pub Date : 2023-12-01 DOI: 10.1016/S1872-5805(23)60783-8
Ming-xia Zhou , Wen-hua Zhou , Xiang Long , Shao-kuan Zhu , Peng Xu , Quan-sheng OuYang , Bin Shi , Jiao-jing Shao

A commercial polypropylene (PP) separator was modified by a one-dimensional carbon nanotube (CNT) and two-dimensional montmorillonite (MMT) hybrid material (CNT-MMT). Because of the high electron conductivity of the CNTs, and the strong polysulfide (LiPS) adsorption ability and easy lithium ion transport through MMT, the interconnected porous CNT-MMT interlayer with excellent structural integrity strongly suppresses LiPS shuttling while maintaining high lithium-ion transport, producing a high utilization of the active sulfur. Lithium-sulfur batteries assembled with this interlayer have a high lithium-ion diffusion coefficient, a high discharge capacity and stable cycling performance. They had an initial specific capacity of 1 373 mAh g−1 at 0.1 C, and a stable cycling performance with a low decay rate of 0.062% per cycle at 1 C after 500 cycles.

一维碳纳米管(CNT)和二维蒙脱石(MMT)混合材料(CNT-MMT)对商用聚丙烯(PP)隔膜进行了改性。由于碳纳米管具有高电子传导性,而蒙脱土具有很强的多硫化物(LiPS)吸附能力,且易于通过蒙脱土进行锂离子传输,因此具有良好结构完整性的互联多孔碳纳米管-蒙脱土夹层可在保持高锂离子传输的同时强力抑制 LiPS 的穿梭,从而产生较高的活性硫利用率。使用这种中间膜组装的锂硫电池具有高锂离子扩散系数、高放电容量和稳定的循环性能。它们在 0.1 摄氏度时的初始比容量为 1 373 mAh g-1,循环性能稳定,在 1 摄氏度时循环 500 次后,衰减率低至 0.062%。
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引用次数: 0
A one-pot method to prepare a multi-metal sulfide/carbon composite with a high lithium-ion storage capability 制备具有高锂离子存储能力的多金属硫化物/碳复合材料的一锅法
IF 5.7 3区 材料科学 Q2 Materials Science Pub Date : 2023-12-01 DOI: 10.1016/S1872-5805(23)60781-4
Wei-cai Zhang , Chao-wei Yang , Shu-yu Hu , Ya-wei Fang , Xiao-min Lin , Zhuo-hao Xie , Ming-tao Zheng , Ying-liang Liu , Ye-ru Liang

Because of their high electrochemical activity, good structural stability, and abundant active sites, multi-metal sulfide/carbon (MMS/C) composites are of tremendous interest in diverse fields, including catalysis, energy, sensing, and environmental science. However, their cumbersome, inefficient, and environmentally unfriendly synthesis is hindering their practical application. We report a straightforward and universal method for their production which is based on homogeneous multi-phase interface engineering. The method has enabled the production of 14 different MMS/C composites, as examples, with well-organized composite structures, different components, and dense heterointerfaces. Because of their composition and structure, a typical composite has efficient, fast, and persistent lithium-ion storage. A ZnS-Co9S8/C composite anode showed a remarkable rate performance and an excellent capacity of 651 mAh·g−1 at 0.1 A·g−1 after 600 cycles. This work is expected to pave the way for the easy fabrication of MMS/C composites.

多金属硫化物/碳(MMS/C)复合材料具有很高的电化学活性、良好的结构稳定性和丰富的活性位点,因此在催化、能源、传感和环境科学等多个领域都有着巨大的应用价值。然而,其繁琐、低效和不环保的合成方法阻碍了其实际应用。我们报告了一种基于均相多相界面工程的直接而通用的方法。以 14 种不同的 MMS/C 复合材料为例,这些复合材料结构合理、成分各异且具有致密的异质界面。由于其成分和结构,典型的复合材料具有高效、快速和持久的锂离子存储能力。一种 ZnS-Co9S8/C 复合负极显示出显著的速率性能,在 0.1 A-g-1 的条件下,循环 600 次后可达到 651 mAh-g-1 的出色容量。这项工作有望为轻松制造 MMS/C 复合材料铺平道路。
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引用次数: 0
Effect of chemical vapor infiltration on the flexural properties of C/C-SiC composites prepared by the precursor infiltration pyrolysis method 化学气相渗透对前驱体渗透热解法制备的 C/C-SiC 复合材料弯曲性能的影响
IF 5.7 3区 材料科学 Q2 Materials Science Pub Date : 2023-12-01 DOI: 10.1016/S1872-5805(23)60732-2
Lin-tao Jia, Meng-qian Wang, Xiao-feng Guo, Jie Zhu, Ai-jun Li, Yu-qing Peng

Carbon/carbon-silicon carbide (C/C-SiC) composites were prepared by impregnation, hot-pressing with curing, carbonization at 800 oC and high-temperature heat treatment (800-1600 oC) using a 2D laminated carbon cloth as the reinforcing filler, and furfurone resin mixed with silicon, carbon from furfurone resin and SiC powders as the matrix. The effects of the addition of the three powders as well as subsequent chemical vapor infiltration (CVI) by methane on the density, microstructure and bend strength of the composites were investigated by scanning electron microscopy, density measurements, X-ray diffraction and mechanical testing. Both the SiC powders formed by the reaction at 1 600 oC between the added Si and C particles and the added SiC powder, play a role in the reinforcement of the materials. In three-point bending, the composites had a pseudoplastic fracture mode and showed interlaminar cracking. After 10 h CVI with methane, pyrolytic carbon was formed at the interface between some of the carbon fibers and the resin carbon matrix, which produced maximum increases in the density and flexural strength of the composites of 4.98% and 38.86%, respectively.

以二维层压碳布为增强填料,以掺硅的呋喃酮树脂、呋喃酮树脂中的碳和碳化硅粉末为基体,通过浸渍、热压固化、800 oC碳化和高温热处理(800-1600 oC)制备了碳/碳化硅(C/C-SiC)复合材料。通过扫描电子显微镜、密度测定、X 射线衍射和机械测试,研究了三种粉末的添加以及随后的甲烷化学气相渗透(CVI)对复合材料密度、微观结构和弯曲强度的影响。添加的 Si 和 C 颗粒在 1600 oC 下反应形成的 SiC 粉末和添加的 SiC 粉末都对材料起到了增强作用。在三点弯曲中,复合材料具有假塑性断裂模式,并出现层间开裂。在与甲烷进行 10 h 的碳化 VI 后,部分碳纤维与树脂碳基体之间的界面上形成了热解碳,从而使复合材料的密度和抗弯强度最大分别增加了 4.98% 和 38.86%。
{"title":"Effect of chemical vapor infiltration on the flexural properties of C/C-SiC composites prepared by the precursor infiltration pyrolysis method","authors":"Lin-tao Jia,&nbsp;Meng-qian Wang,&nbsp;Xiao-feng Guo,&nbsp;Jie Zhu,&nbsp;Ai-jun Li,&nbsp;Yu-qing Peng","doi":"10.1016/S1872-5805(23)60732-2","DOIUrl":"10.1016/S1872-5805(23)60732-2","url":null,"abstract":"<div><p>Carbon/carbon-silicon carbide (C/C-SiC) composites were prepared by impregnation, hot-pressing with curing, carbonization at 800 <sup>o</sup>C and high-temperature heat treatment (800-1600 <sup>o</sup>C) using a 2D laminated carbon cloth as the reinforcing filler, and furfurone resin mixed with silicon, carbon from furfurone resin and SiC powders as the matrix. The effects of the addition of the three powders as well as subsequent chemical vapor infiltration (CVI) by methane on the density, microstructure and bend strength of the composites were investigated by scanning electron microscopy, density measurements, X-ray diffraction and mechanical testing. Both the SiC powders formed by the reaction at 1 600 <sup>o</sup>C between the added Si and C particles and the added SiC powder, play a role in the reinforcement of the materials. In three-point bending, the composites had a pseudoplastic fracture mode and showed interlaminar cracking. After 10 h CVI with methane, pyrolytic carbon was formed at the interface between some of the carbon fibers and the resin carbon matrix, which produced maximum increases in the density and flexural strength of the composites of 4.98% and 38.86%, respectively.</p></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":null,"pages":null},"PeriodicalIF":5.7,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138556499","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
3D porous NiCo2(CO3)3/reduced graphene oxide aerogel with heterogeneous interfaces for high-efficiency microwave absorption 具有异质界面的三维多孔镍钴(CO3)3/还原氧化石墨烯气凝胶用于高效微波吸收
IF 5.7 3区 材料科学 Q2 Materials Science Pub Date : 2023-12-01 DOI: 10.1016/S1872-5805(23)60780-2
Dan-dan Wu , Han-xiao Zhang , Zheng-yan Wang , Yan-lan Zhang , Yong-zhen Wang

Advanced electromagnetic absorbing materials (EAMs) with strong absorption and a wide effective absorption bandwidth (EAB), using innovative microstructural design and suitable multicomponents remain a persistent challenge. Here, we report the production of a material by the hydrothermal reduction of a mixture of graphene oxide (GO), Ni(NO3)2·6H2O, and Co(NO3)2·6H2O, resulting in reduced GO (RGO) with a self-assembled 3D mesh structure filled with NiCo2(CO3)3. The unique microstructure of this assembly not only solves the problem of NiCo2(CO3)3 particles agglomerating but also changes the electromagnetic parameters, thereby improving the impedance matching and attenuation ability. High electromagnetic wave absorption (EMA) was achieved by combining the 3D interconnected mesh structure and the various interfaces between NiCo2(CO3)3 and RGO. The minimal reflection loss (RLmin) was −58.5 dB at 2.3 mm, and the EAB was 6.5 GHz. The excellent EMA performance of the aerogel can be attributed to the multiple reflection, scattering, and relaxation process of the porous 3D structure as well as the strong polarization of the interfacial matrix.

利用创新的微结构设计和合适的多组分制造具有强吸收能力和宽有效吸收带宽(EAB)的先进电磁吸收材料(EAMs)仍然是一项持久的挑战。在此,我们报告了通过水热还原氧化石墨烯(GO)、Ni(NO3)2-6H2O 和 Co(NO3)2-6H2O 的混合物,制备出具有填充 NiCo2(CO3)3 的自组装三维网状结构的还原型 GO(RGO)材料。通过结合三维互联网状结构以及 NiCo2(CO3)3 和 RGO 之间的各种界面,实现了高电磁波吸收(EMA)。2.3 mm 时的最小反射损耗(RLmin)为 -58.5 dB,EAB 为 6.5 GHz。气凝胶优异的 EMA 性能可归因于多孔三维结构的多重反射、散射和弛豫过程以及界面基质的强极化。
{"title":"3D porous NiCo2(CO3)3/reduced graphene oxide aerogel with heterogeneous interfaces for high-efficiency microwave absorption","authors":"Dan-dan Wu ,&nbsp;Han-xiao Zhang ,&nbsp;Zheng-yan Wang ,&nbsp;Yan-lan Zhang ,&nbsp;Yong-zhen Wang","doi":"10.1016/S1872-5805(23)60780-2","DOIUrl":"10.1016/S1872-5805(23)60780-2","url":null,"abstract":"<div><p>Advanced electromagnetic absorbing materials (EAMs) with strong absorption and a wide effective absorption bandwidth (EAB), using innovative microstructural design and suitable multicomponents remain a persistent challenge. Here, we report the production of a material by the hydrothermal reduction of a mixture of graphene oxide (GO), Ni(NO<sub>3</sub>)<sub>2</sub>·6H<sub>2</sub>O, and Co(NO<sub>3</sub>)<sub>2</sub>·6H<sub>2</sub>O, resulting in reduced GO (RGO) with a self-assembled 3D mesh structure filled with NiCo<sub>2</sub>(CO<sub>3</sub>)<sub>3</sub>. The unique microstructure of this assembly not only solves the problem of NiCo<sub>2</sub>(CO<sub>3</sub>)<sub>3</sub> particles agglomerating but also changes the electromagnetic parameters, thereby improving the impedance matching and attenuation ability. High electromagnetic wave absorption (EMA) was achieved by combining the 3D interconnected mesh structure and the various interfaces between NiCo<sub>2</sub>(CO<sub>3</sub>)<sub>3</sub> and RGO. The minimal reflection loss (<em>RL</em><sub>min</sub>) was −58.5 dB at 2.3 mm, and the EAB was 6.5 GHz. The excellent EMA performance of the aerogel can be attributed to the multiple reflection, scattering, and relaxation process of the porous 3D structure as well as the strong polarization of the interfacial matrix.</p></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":null,"pages":null},"PeriodicalIF":5.7,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138556927","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Contribution of surface roughness and oxygen-containing groups to the interfacial shear strength of carbon fiber/epoxy resin composites 表面粗糙度和含氧基团对碳纤维/环氧树脂复合材料界面剪切强度的影响
IF 5.7 3区 材料科学 Q2 Materials Science Pub Date : 2023-12-01 DOI: 10.1016/S1872-5805(23)60720-6
Yi-cai Liang , Xing-hua Zhang , Xing-hai Wei , De-qi Jing , Wei-guo Su , Shou-chun Zhang

The interfacial shear strength (IFSS) between carbon fibers (CFs) and the matrix is crucial to the performance of CF-reinforced polymer composites. To evaluate the contribution of mechanical interlocking and chemical anchoring at the interfaces of a polyacrylonitrile-based CF (TORAYCA T800SC-12000-10E)-reinforced epoxy resin (EP: bisphenol A type epoxy resin and tetrafunctional epoxy resin) composites, the surface roughness and content of oxygen-containing functional groups of the CFs were respectively altered by ammonia treatment and electrochemical oxidation. The results showed that ammonia treatment increased the surface roughness without much change to the surface elemental composition, while electrochemical oxidation increased the number of surface oxygen groups without changing the surface roughness. The IFSS of CF/EP composites was tested by the micro-droplet method. The relationships between IFSS, and surface roughness and oxygen content were obtained by linear fitting. The results showed that in the interfacial bonding of CF to epoxy resin, the contribution of chemical anchoring to the IFSS is larger than that of mechanical interlocking.

碳纤维(CF)与基体之间的界面剪切强度(IFSS)对碳纤维增强聚合物复合材料的性能至关重要。为了评估聚丙烯腈基碳纤维(东丽凯 T800SC-12000-10E)增强环氧树脂(EP:双酚 A 型环氧树脂和四官能团环氧树脂)复合材料界面的机械互锁和化学锚固作用,分别采用氨处理和电化学氧化法改变了碳纤维的表面粗糙度和含氧官能团的含量。结果表明,氨处理增加了表面粗糙度,但表面元素组成没有太大变化;而电化学氧化增加了表面含氧基团的数量,但表面粗糙度没有变化。微滴法测试了 CF/EP 复合材料的 IFSS。通过线性拟合得出了 IFSS 与表面粗糙度和氧含量之间的关系。结果表明,在 CF 与环氧树脂的界面粘合中,化学锚固对 IFSS 的贡献大于机械互锁。
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引用次数: 0
A highly efficient, rapid, room temperature synthesis method for coal-based water-soluble fluorescent carbon dots and its use in Fe3+ ion detection 煤基水溶性荧光碳点的高效、快速、室温合成方法及其在 Fe3+ 离子检测中的应用
IF 5.7 3区 材料科学 Q2 Materials Science Pub Date : 2023-12-01 DOI: 10.1016/S1872-5805(23)60706-1
Zhong-fu Cheng , Xue-yan Wu , Lei Liu , Long He , Zu-guo Yang , Chang Cao , Yan Lu , Ji-xi Guo

We report a method for the of coal-based fluorescent carbon dots (CDs) at room temperature using a mixture of hydrogen peroxide (H2O2) and formic acid (HCOOH) as the oxidant instead of concentrated HNO3 or H2SO4. The CDs have an excitation dependent behavior with a high quantum yield (QY) of approximately 7.2%. The CDs are water soluble and have excellent photo-stability, good resistance to salt solutions, and are insensitive to pH in a range of 2.0-12.0. The CDs were used as a very sensitive probe for the turn-off sensing of Fe3+ ion with a detection limit as low as 600 nmol/L and a detection range from 2 to 100 μmol/L. This work provides a way for the high value-added utilization of coal.

我们报告了一种在室温下利用过氧化氢(H2O2)和甲酸(HCOOH)的混合物作为氧化剂而不是浓 HNO3 或 H2SO4 来制备煤基荧光碳点(CD)的方法。这种 CD 具有与激发相关的特性,量子产率(QY)高达约 7.2%。这种光盘可溶于水,具有出色的光稳定性和良好的耐盐溶液性,对 pH 值(2.0-12.0)不敏感。这种 CD 被用作一种非常灵敏的探针,用于 Fe3+ 离子的关断感应,其检测限低至 600 nmol/L,检测范围为 2 至 100 μmol/L。这项工作为煤炭的高附加值利用提供了一条途径。
{"title":"A highly efficient, rapid, room temperature synthesis method for coal-based water-soluble fluorescent carbon dots and its use in Fe3+ ion detection","authors":"Zhong-fu Cheng ,&nbsp;Xue-yan Wu ,&nbsp;Lei Liu ,&nbsp;Long He ,&nbsp;Zu-guo Yang ,&nbsp;Chang Cao ,&nbsp;Yan Lu ,&nbsp;Ji-xi Guo","doi":"10.1016/S1872-5805(23)60706-1","DOIUrl":"10.1016/S1872-5805(23)60706-1","url":null,"abstract":"<div><p>We report a method for the of coal-based fluorescent carbon dots (CDs) at room temperature using a mixture of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) and formic acid (HCOOH) as the oxidant instead of concentrated HNO<sub>3</sub> or H<sub>2</sub>SO<sub>4</sub>. The CDs have an excitation dependent behavior with a high quantum yield (QY) of approximately 7.2%. The CDs are water soluble and have excellent photo-stability, good resistance to salt solutions, and are insensitive to pH in a range of 2.0-12.0. The CDs were used as a very sensitive probe for the turn-off sensing of Fe<sup>3+</sup> ion with a detection limit as low as 600 nmol/L and a detection range from 2 to 100 μmol/L. This work provides a way for the high value-added utilization of coal.</p></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":null,"pages":null},"PeriodicalIF":5.7,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138556873","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Carbon-based photothermal materials for the simultaneous generation of water vapor and electricity 同时产生水蒸气和电能的碳基光热材料
IF 5.7 3区 材料科学 Q2 Materials Science Pub Date : 2023-12-01 DOI: 10.1016/S1872-5805(23)60785-1
Zi-han Qiu , Guan-yu Zhao , Yang Sun , Xu-zhen Wang , Zong-bin Zhao , Jie-shan Qiu

Solar-driven interfacial vapor generation (SIVG) is increasingly used for fresh water production, having the advantages of low energy consumption, eco-friendliness, and high efficiency. Carbon-based photothermal materials (CPTMs) can introduce temperature and salinity gradients in the SIVG process because of their outstanding photothermal conversion properties, which have given SIVG great potential for both steam and power generation. Various kinds of CPTMs for clean water and electricity generation are discussed in this review. The basic principles and key performance indices of SIVG are first described and the photothermal and SIVG performance of various CPTMs including graphene oxides, carbon nanotubes, carbon dots and carbonized biomass are then summarized. Finally, current research concerning water/electricity cogeneration and ways to deal with the problems encountered are presented, to provide some guidelines for the use of multifunctional CPTMs for simultaneous steam and electricity generation.

太阳能驱动界面蒸汽发生技术(SIVG)具有能耗低、生态友好和效率高等优点,正越来越多地用于淡水生产。碳基光热材料(CPTMs)因其出色的光热转换特性,可在 SIVG 过程中引入温度和盐度梯度,这使得 SIVG 在蒸汽和发电方面具有巨大潜力。本综述讨论了各种用于清洁水和发电的 CPTM。首先介绍了 SIVG 的基本原理和关键性能指标,然后总结了各种 CPTM(包括石墨烯氧化物、碳纳米管、碳点和碳化生物质)的光热和 SIVG 性能。最后,介绍了目前有关水/电热电联产的研究以及解决所遇到问题的方法,为使用多功能 CPTM 同时产生蒸汽和电力提供了一些指导。
{"title":"Carbon-based photothermal materials for the simultaneous generation of water vapor and electricity","authors":"Zi-han Qiu ,&nbsp;Guan-yu Zhao ,&nbsp;Yang Sun ,&nbsp;Xu-zhen Wang ,&nbsp;Zong-bin Zhao ,&nbsp;Jie-shan Qiu","doi":"10.1016/S1872-5805(23)60785-1","DOIUrl":"10.1016/S1872-5805(23)60785-1","url":null,"abstract":"<div><p>Solar-driven interfacial vapor generation (SIVG) is increasingly used for fresh water production, having the advantages of low energy consumption, eco-friendliness, and high efficiency. Carbon-based photothermal materials (CPTMs) can introduce temperature and salinity gradients in the SIVG process because of their outstanding photothermal conversion properties, which have given SIVG great potential for both steam and power generation. Various kinds of CPTMs for clean water and electricity generation are discussed in this review. The basic principles and key performance indices of SIVG are first described and the photothermal and SIVG performance of various CPTMs including graphene oxides, carbon nanotubes, carbon dots and carbonized biomass are then summarized. Finally, current research concerning water/electricity cogeneration and ways to deal with the problems encountered are presented, to provide some guidelines for the use of multifunctional CPTMs for simultaneous steam and electricity generation.</p></div>","PeriodicalId":19719,"journal":{"name":"New Carbon Materials","volume":null,"pages":null},"PeriodicalIF":5.7,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138556924","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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New Carbon Materials
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