Porous nitrogen-enriched hollow carbon nanofibers as freestanding electrode for enhanced lithium storage

One-dimensional porous carbons bearing high surface areas and sufficient heteroatom doped functional-ities are essential for advanced electrochemical energy storage devices, especially for developing free-standing film electrodes. Here we develop a porous, nitrogen-enriched, freestanding hollow carbon nanofiber (PN-FHCF) electrode material via filtration of polypyrrole (PPy) hollow nanofibers formed by in situ self-degraded template-assisted strategy, followed by NH3-assisted carbonization. The PN-FHCF retains the freestanding film morphology that is composed of three-dimensional networks from the entanglement of 1D nanofiber and delivers 3.7-fold increase in specific surface area (592 m2·g-1) com-pared to the carbon without NH3 treatment (FHCF). In spite of the enhanced specific surface area, PN-FHCF still exhibits comparable high content of surface N functionalities (8.8％, atom fraction) to FHCF. Such developed hierarchical porous structure without sacrificing N doping functionalities together enables the achievement of high capacity, high-rate property and good cycling stability when applied as self-supporting anode in lithium-ion batteries, superior to those of FHCF without NH3 treatment.     

Synthesis of CuTi-LDH supported on g-C3N4 for electrochemical and photoelectrochemical oxygen evolution reactions

A nanocomposite CuTi layered double hydroxide (LDH) supported on g-C₃N₄ (15 wt% of g-C₃N₄) is facilely synthesized by hydrothermal method. There are electrostatic interactions between positive layers of CuTi-LDH and negatively charged inner g-C₃N₄ sheets. The nanocomposite and its precursors are characterized through various analytical techniques, which affirmed the presence of both g-C₃N₄ and CuTi-LDH characteristic features. The pore-enriched hybrid geometry of CuTi-LDH@g-C₃N₄ with high specific surface area (146 m²/g), and suitable band gap of 2.46 eV enables the nanocomposite to act as both an electrocatalyst and photoelectrocatalyst for oxygen evolution reaction (OER). Both the electrochemical and photoelectrochemical studies are done using 1 M KOH (pH = 13.6) with applied potential of ?0.2 V to 1.5 V vs. Ag/AgCl. The onset potential of CuTi-LDH@g-C₃N₄ for OER appears at η = 0.36 V in dark and η = 0.32 V under visible light illumination of 30 min. Also, Mott-Schottky analysis shows n-type semiconductor behaviour for CuTi-LDH@g-C₃N₄ and its precursors. The photoelectrochemical water oxidation proceeds by charge transfer across a Type II heterojunction formed between the CuTi-LDH and g-C₃N₄ materials.     

Mechanochemically assisted fabrication of ultrafine Pd nanoparticles on natural waste-derived nitrogen-doped porous carbon for the efficient formic acid decomposition

Utilizing natural waste as carbon source to prepare porous carbon with ultrahigh surface area and developing a facile protocol to synthesize supported metal nanoparticles toward an efficient formic acid (FA) decomposition are vital but remains challenging. Here, discarded ginkgo leaves were utilized as carbon source to prepare ginkgo leaf-derived porous carbon (GLPC) with an ultrahigh surface area of 3851 m²/g. Based on the as-prepared nitrogen-doped GLPC (N-GLPC) after “soft” nitriding, a facile solid-state reduction strategy with mortar-pestle grinding and without the use of any organic solvent and stabilizing ligand was developed to synthesize ultrafine and well-distributed Pd nanoparticles (NPs) with a diameter of 2.7 ± 0.7 nm. The “soft” nitriding temperature and addition of base during preparation played vital roles in the activity of the fabricated catalysts. The Pd/N-GLPC-350 exhibited the highest catalytic activity toward decomposing FA, achieving a high turnover frequency of 2952 h^?1 at 333 K. The Pd/N-GLPC-350 was quite stable and could be reused at least five times without evident activity loss. This study provides a facile solid-state reduction protocol with mortar-pestle grinding to synthesize metal NPs by using natural waste-derived porous carbon as support toward efficient FA decomposition.     

Two-step pyrolytic engineering to form porous nitrogen-rich carbons with a 3D network structure for Zn-air battery oxygen reduction electrocatalysis

It is of great urgency to design inexpensive and high-performance oxygen reduction reaction (ORR) electrocatalysts derived from biowastes as substitutes for Pt-based materials in electrochemical energy-conversion devices. Here we propose a strategy to synthesize three-dimensional (3D) porous nitrogen-doped network carbons to catalyze the ORR from two-step pyrolysis engineering of biowaste scale combined with the use of a ZnCl₂ activator and a FeCl₂ promotor. Electrochemical tests show that the synthesized network carbons have exhibited comparable ORR catalytic activity with a half-wave potential (~0.85 V vs. RHE) and outstanding cyclical stability in comparison to the Pt/C catalyst. Beyond that, a high electron transfer number (~3.8) and a low peroxide yield (<7.6%) can be obtained, indicating a four-electron reaction pathway. The maximum power density is ~68 mW cm^?2, but continuous discharge curves (at a constant potential of ~1.30 V) for 12 h are not obviously declined in Zn-air battery tests using synthesized network carbons as the cathodic catalyst. The formation of 3D porous structures with high BET surface area can effectively expose the surface catalytic sites and promote mass transportation to boost the ORR activity. This work may open a new idea to prepare porous carbon-based catalysts for some important reactions in new energy devices.     

Platinum nanoparticles decorated on graphitic carbon nitride-ZIF-67 composite support: An electrocatalyst for the oxidation of butanol in fuel cell applications

In the present study, we report an eco-friendly and simple route to design and synthesize novel nanocomposite catalyst based on platinum nanoparticles anchored on binary support of graphitic carbon nitride (g-C₃N₄) and cobalt-metal-organic framework (ZIF-67). For this purpose, ZIF-67 was prepared by precipitation method and g-C₃N₄ was prepared through thermal polymerization method. Later, ZIF-67 and g-C₃N₄ were hybridized through sonication to get homogeneous g–C₃N₄–ZIF-67 nanocomposite support material. Platinum nanoparticles (PtNPs) were uniformly deposited on g–C₃N₄–ZIF-67 by an electrochemical method. The as-developed nanocatalyst was characterized by morphological, structural and electrochemical techniques. The electrocatalytic activity of PtNPs@g–C₃N₄–ZIF-67 nanocatalyst towards butanol oxidation was evaluated via CV, CA, LSV and EIS in an alkaline medium. Results revealed that the proposed catalyst showed greatly enhanced electrooxidation of butanol in terms of high magnificent current density, lower oxidation potential, excellent long-term stability, large surface area, low charge transfer resistance and less toxic ability. Enhanced catalytic performance of the proposed catalyst could be ascribed to the synergistic effect of g–C₃N₄–ZIF-67 nanocomposite and PtNPs. The PtNPs@g–C₃N₄–ZIF-67 catalyst holds promising potential applications to be used as an anodic electrocatalyst for the development of high-performance alkaline fuel cells.     

The effects of warmth and CO2 concentration,with and without bioeffluents,on the emission of CO2 by occupants and physiological responses

The emission rate of carbon dioxide (CO₂) depends on many factors but mainly on the activity level (metabolic rate) of occupants. In this study, we examined two other factors that may influence the CO₂ emission rate, namely the background CO₂ concentration and the indoor temperature. Six male volunteers sat one by one in a 1.7 m³ chamber for 2.5 h and performed light office-type work under five different conditions with two temperature levels (23 vs. 28°C) and three background concentrations of CO₂ (800 vs. 1400 vs. 3000 ppm). Background CO₂ levels were increased either by dosing CO₂ from a cylinder or by reducing the outdoor air supply rate. Physiological responses to warmth, added CO₂, and bioeffluents were monitored. The rate of CO₂ emission was estimated using a mass-balance equation. The results indicate a higher CO₂ emission rate at the higher temperature, at which the subjects were warm, and a lower emission rate in all conditions in which the background CO₂ concentration increased. Physiological measurements partially explained the present results but more measurements are needed.     

利用碳钢铸坯组织灰度图获取C含量分布的方法

摘要：基于热酸洗腐蚀原理与图像光学理论，提出运用金属低倍组织灰度分析技术（灰度分析法）获取中高碳钢铸坯的低倍组织中不同位置不同区域不同尺度的一维、二维C元素含量分布。偏析严重的位置得到的C元素含量高，初始凝固的晶粒中心位置得到的C元素含量低，说明通过灰度分析法计算的C元素含量分布能与低倍组织形貌很好地对应。同时，通过电子探针与灰度分析法的测量结果对比，发现二者C元素含量的变化趋势具有很好的一致性，这验证了灰度分析法的有效性。另外，低倍组织图像整体亮度的改变不会造成由灰度分析法所测量的C元素含量发生明显改变，则表明灰度分析法对测量环境的变化具有一定的抗干扰能力，也间接说明了其可靠性。     

Improved rheological properties and stability of multiwalled carbon nanotubes/polymer in harsh environment

This work aims to improve the rheological properties and stability of multiwalled carbon nanotubes (MWCNTs)/acrylamide (AA) base skeleton polymer blends at harsh environment of high salinity-high temperature (HS-HT) or various pH. Different co/terpolymers have been accomplished to modify the structure of AA polymer by free-radical copolymerization of AA-based monomers. Anionic, cationic, and hydrophobic functional groups were used for the synthesis of polyelectrolyte, polyampholytic, and partially hydrophobic AA polymer types. The conversion, molecular weight, and poly dispersity of co/terpolymers have been evaluated by nuclear magnetic resonance (¹H-NMR), gel permeation chromatography, and differential scanning calorimetry analysis. The effects of sonication power, concentration of polymer, and concentration of MWCNTs were also investigated on rheological behavior of co/terpolymers. The results show that negative polyelectrolyte and polyampholytic polymers are the best candidates for the improvement of MWCNTs/polymer stability and viscosity at HS-HT and alkali environment, respectively. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47205.     

碳纤维复合材料薄壁圆筒的轴向导热系数测试

碳纤维复合材料薄壁圆筒为各向异性导热，其轴向导热系数是筒体温度场理论计算、成型工艺优化的重要参数。碳纤维复合材料圆筒由于较小的截面面积给筒体加热、热量有效传递带来了较大困难。本文以平板材料导热系数的稳态法测试国家标准为基础，基于傅里叶一维稳态导热原理，设计了一套用于薄壁圆筒轴向导热系数测试的装置，采用双试件对称加热、辐射换热防护及热对流环境控制等实现了热量沿筒体轴向的有效传导，利用该装置对导热系数已知的铝筒进行测试，验证了该装置设计的可行性，得到了碳纤维复合材料薄壁圆筒的轴向导热系数为（4.60±0.13） W/(m•K)。