Sandwich-type composited solid polymer electrolytes to strengthen the interfacial ionic transportation and bulk conductivity for all-solid-state lithium batteries from room temperature to 120℃

The insurmountable charge transfer impedance at the Li metal/solid polymer electrolytes(SPEs)interface at room temperature as well as the ascending risk of short circuits at the operating temperature higher than the melting point,dominantly limits their applications in solid-state batteries(SSBs).Although the inorganic filler such as CeO_(2)nanoparticle content of composite solid polymer electrolytes(CSPEs)can significantly reduce the enormous charge transfer impedance at the Li metal/SPEs interface,we found that the required content of CeO_(2)nanoparticles in SPEs varies for achieving a decent interfacial charge transfer impedance and the bulk ionic conductivity in CSPEs.In this regard,a sandwich-type composited solid polymer electrolyte with a 10%CeO_(2)CSPEs interlayer sandwiched between two 50%CeO_(2)CSPEs thin layers(sandwiched CSPEs)is constructed to simultaneously achieve low charge transfer impedance and superior ionic conductivity at 30℃.The sandwiched CSPEs allow for stable cycling of Li plating and stripping for 1000 h with 129 mV polarized voltage at 0.1 mA cm^(-2)and 30℃.In addition,the LiFePO_(4)/Sandwiched CSPEs/Li cell also exhibits exceptional cycle performance at 30℃and even elevated120℃without short circuits.Constructing multi-layered CSPEs with optimized contents of the inorganic fillers can be an efficient method for developing all solid-state PEO-based batteries with high performance at a wide range of temperatures.

粤港澳大湾区PBL SO2的遥感监测研究

利用Aura卫星搭载的臭氧观测仪反演的大气边界层SO2(PBL SO2)柱含量数据,分析了自2005年以来粤港澳大湾区PBL SO2柱含量的空间分布特征、变化趋势及其影响的原因。结果显示了粤港澳大湾区PBL SO2柱含量2005-2018年呈减少的趋势,2005年年平均PBL SO2柱含量为0.551 DU,2018年为0.431 DU,减少了0.12 DU,约为21.8%。最小值出现在2013年4月,区域月平均PBL SO2柱含量为(0.316±0.135)DU。在高值秋冬季节PBL SO2呈现较大的下降趋势;在低值春夏季节PBL SO2保持着相近的水平,大约在0.380DU处上下波动。小波系数显示了PBL SO2的变化在10个月的尺度水平上存在明显的周期变化。粤港澳大湾区PBL SO2月变化在时间和空间上存在明显的差异。最小值和最大值分别出现在3月和10月,多年平均值大约分别为(0.404±0.053)DU和(0.565±0.089)DU,10月份整个区域的PBL SO2保持在最高的水平。波动最大出现在7月,变异系数为0.19;而在2月波动最小,变异系数约为0.10。粤港澳大湾区SO2污染严重的地区出现在中部,多年平均PBL SO2柱含量值可达0.600 DU,同时年际间的波动较大;PBL SO2较低的区域主要在东部的惠州市和北部的肇庆,2005-2018年平均的PBL SO2约为0.400 DU,年际间的波动较小。2005-2018年PBL SO2的变化趋势在不同空间上呈现明显差异,变化范围为-0.450~0.290 DU,百分比范围为-55%~65%。PBL SO2出现增长的地区主要是在低值区;在高值区,PBL SO2表现出较大的减少,减少最多的是中山市、广州市和佛山市的交界处,减少了约0.450 DU,约为55%。

Strategy and Future Prospects to Develop Room-Temperature-Recoverable NO2 Gas Sensor Based on Two-Dimensional Molybdenum Disulfide

Nitrogen dioxide(NO2),a hazardous gas with acidic nature,is continuously being liberated in the atmosphere due to human activity.The NO2 sensors based on traditional materials have limitations of high-temperature requirements,slow recovery,and performance degradation under harsh environmental conditions.These limitations of traditional materials are forcing the scientific community to discover future alternative NO2 sensitive materials.Molybdenum disulfide(MoS2)has emerged as a potential candidate for developing next-generation NO2 gas sensors.MoS2 has a large surface area for NO2 molecules adsorption with controllable morphologies,facile integration with other materials and compatibility with internet of things(IoT)devices.The aim of this review is to provide a detailed overview of the fabrication of MoS2 chemiresistance sensors in terms of devices(resistor and transistor),layer thickness,morphology control,defect tailoring,heterostructure,metal nanoparticle doping,and through light illumination.Moreover,the experimental and theoretical aspects used in designing MoS2-based NO2 sensors are also discussed extensively.Finally,the review concludes the challenges and future perspectives to further enhance the gas-sensing performance of MoS2.Understanding and addressing these issues are expected to yield the development of highly reliable and industry standard chemiresistance NO2 gas sensors for environmental monitoring.

Theoretical Prediction of the Intrinsic Half-metallicity in One-dimensional Cr2NO2 Nanoribbons

One-dimensional Cr2NO2 nanoribbons cut from the oxygen-passivated Cr2NO2 MXene were investigated by using density functional theory. The wide nanoribbons have ferromagnetic ground states and are intrinsic half-metals, independent of their chirality. The half-metallic band gaps of wide nanoribbons are larger than 1 eV, which are large enough for avoiding thermally activated spin flip. The magnetism does not rely on the edge states but originates from all the Cr atoms. Furthermore, the half-metallicity is still robust in an electronic device even if the bias is up to 1 V. Therefore, one-dimensional Cr2NO2 nanoribbons are good candidates for spintronics.

A High-Temperature β-Phase NaMnO2 Stabilized by Cu Doping and Its Na Storage Properties

The high-temperature β-phase NaMnO2 is a promising material for Na-ion batteries（NIBs） due to its high capacity and abundant resources. However, the synthesis of phase-pure -NaMnO2 is burdensome and costineffective because it needs to be sintered under oxygen atmosphere at high temperature and followed by a quenching procedure. Here we first report that the pure β phase can be stabilized by Cu-doping and easily synthesized by replacing a proportion of Mn with Cu via a simplified process including sintering in air and cooling to room temperature naturally. Based on the first-principle calculations, the band gap decreases from 0.7 eV to 0.3 eV, which indicates that the electronic conductivity can be improved by Cu-doping. The designed -NaCu（0.1）Mn（0.9）O2 is applied as cathode in NIBs, exhibiting an energy density of 419 Wh/kg and better performance in terms of rate capability and cycling stability than those in the undoped case.

Atomic Modulation of 3D Conductive Frameworks Boost Performance of MnO2 for Coaxial Fiber‑Shaped Supercapacitors

Coaxial fiber-shaped supercapacitors are a promising class of energy storage devices requiring high performance for flexible and miniature electronic devices.Yet,they are still struggling from inferior energy density,which comes from the limited choices in materials and structure used.Here,Zn-doped CuO nanowires were designed as 3D framework for aligned distributing high mass loading of MnO2 nanosheets.Zn could be introduced into the CuO crystal lattice to tune the covalency character and thus improve charge transport.The Zn–CuO@MnO2 as positive electrode obtained superior performance without sacrificing its areal and gravimetric capacitances with the increasing of mass loading of MnO2 due to 3D Zn–CuO framework enabling efficient electron transport.A novel category of free-standing asymmetric coaxial fiber-shaped supercapacitor based on Zn0.11CuO@MnO2 core electrode possesses superior specific capacitance and enhanced cell potential window.This asymmetric coaxial structure provides superior performance including higher capacity and better stability under deformation because of sufficient contact between the electrodes and electrolyte.Based on these advantages,the as-prepared asymmetric coaxial fiber-shaped supercapacitor exhibits a high specific capacitance of 296.6 mF cm^−2 and energy density of 133.47μWh cm^−2.In addition,its capacitance retention reaches 76.57%after bending 10,000 times,which demonstrates as-prepared device’s excellent flexibility and long-term cycling stability.

Time-resolved measurements of NO2 concentration in pulsed discharges by high-sensitivity cavity ring-down spectroscopy

To describe the complex kinetics of formation and destruction mechanism of nitrogen dioxide（NO2）, there is an increasing demand for real-time and in situ analysis of NO2 in the discharge region. Pulsed cavity ring-down spectroscopy（CRDS） provides an excellent diagnostic approach. In the present paper, CRDS has been applied in situ for time evolution measurement of NO2 concentration which is rarely investigated in gas discharges. In pulsed direct current discharge of NO2/Ar mixture at a pressure of 500 Pa, a peak voltage of -1300 V and a frequency of 30 Hz, for higher initial NO2 concentration（3.05×10^（14）cm^（-3）, 8.88×10^（13）cm^（-3））,the NO2 concentration sharply decreases at the beginning of the discharge afterglow and then becomes almost constant, and the pace of decline increases with pulse duration; however, for lower initial NO2 concentration of 1.69×10^（13）cm^（-3）, the NO2 concentration also decreases at the beginning of the discharge afterglow for 200 ns and 1 μs pulse durations, while it slightly increases and then declines for 2 μs pulse duration. Thus, the removal of low-level NO2 could not be promoted by a higher mean energy input.

A Multi-Mode Public Transportation System Using Vehicular to Network Architecture

The number of accidents in the campus of Suranaree University of Technology(SUT)has increased due to increasing number of personal vehicles.In this paper,we focus on the development of public transportation system using Intelligent Transportation System(ITS)along with the limitation of personal vehicles using sharing economy model.The SUT Smart Transit is utilized as a major public transportation system,while MoreSai@SUT(electric motorcycle services)is a minor public transportation system in this work.They are called Multi-Mode Transportation system as a combination.Moreover,a Vehicle toNetwork(V2N)is used for developing theMulti-Mode Transportation system in the campus.Due to equipping vehicles with On Board Unit(OBU)and 4G LTE modules,the real time speed and locations are transmitted to the cloud.The data is then applied in the proposed mathematical model for the estimation of Estimated Time of Arrival(ETA).In terms of vehicle classifications and counts,we deployed CCTV cameras,and the recorded videos are analyzed by using You Only Look Once(YOLO)algorithm.The simulation and measurement results of SUT Smart Transit and MoreSai@SUT before the covid-19 pandemic are discussed.Contrary to the existing researches,the proposed system is implemented in the real environment.The final results unveil the attractiveness and satisfaction of users.Also,due to the proposed system,the CO_(2) gas gets reduced when Multi-Mode Transportation is implemented practically in the campus.

Pressure Effects on the Charge Carrier Transportation of BaF_2 Nanocrystals

The charge transport behavior of barium fluoride nanocrystals is investigated by in situ impedance measurement up to 35 GPa. It is found that the parameters change discontinuously at about 6.9 GPa, corresponding to the phase transition of BaF2 nanocrystals under high pressure. The charge carriers in BaF2 nanocrystals include both Fions and electrons. Pressure makes the electronic transport more difficult. The defects at grains dominate the electronic transport process. Pressure could make the charge-discharge processes in the Fm3m phase more difficult.

In-situ Synthesis of SnO2 Quantum Dots/ZnS Nanosheets Heterojunction as a Visible-light-driven Photocatalyst for Degradation of Rhodamine B,Potassium Dichromate and Tetracycline

The SnO2 quantum dots(SnO2QDs)/ZnS nanosheets(ZnSNs)heterojunction was fabricated via an in-situ synthetic method at room temperature.Rhodamine B,potassium dichromate,and tetracycline were used to discuss the photocatalytic activities of the as-prepared samples under the visible light illumination.The photocatalytic mechanism of the as-prepared samples was also proposed.The experimental results indicate that the degradation efficiency of the as-prepared SnO2QDs/ZnSNs heterojunction first increases and then decreases with increasing the usage of ZnSNs.When the mass ratio of SnO2QDs to ZnSNs is 1:2 in 180 min,the as-prepared samples have the highest degradation efficiency of 89.1%for rhodamine B,97.7%for potassium dichromate,and 83.8%for tetracycline,which are much higher than 51.7%,26.8%,and 0.9%of pure SnO2QDs as well as 37.9%,87.1%,and 19.1%of pure ZnSNs,respectively.After it is repeatedly degraded for 3 times,it possesses the degradation efficiency of 62.5%for rhodamine B,which increases by 200.5%in comparison with 20.8%of the pure SnO2QDs.Moreover,the enhanced photocatalytic performances of the as-prepared hybrids are attributed to the formation of heterojunction between the SnO2QDs and ZnSNs.In addition,hydroxyl radicals and superoxide anion radicals play major roles during the photocatalytic degradation process,while holes play a minor role.

CO2 emission of urban passenger transportation in China from 2000 to 2014

This study reviewed the urban passenger transportation(UPT)development of seven typical cities in China from 2000 to 2014,estimated the UPT CO2emission,analyzed the structure,and discussed the main factors of UPT CO,emission.Results showed that increases of GDP,population,and UPT scale of the cities have speeded up.The most significant development of UPT is that the growth of private vehicles is greatly faster than that of public transportation.The total and per-capita UPT CO2 emissions both increased.The share of private vehicles emission to total UPT CO2emission has increased,with the share in range of 65%-88%in 2014,exponentially leading to the increases of total and per-capita UPT CO2 emission.Although UPT CO2 emission structure with more share of public transportation would slow down the UPT CO2emission increase,private vehicle CO2 emission is recognized as the dominated driving factor.Contributions of driving factors,such as GDP,population,private vehicle CO2 emissions,to UPT CO2 emission are different among the cities.Private vehicle CO2 emission.is the dominated factor for UPT CO2emission in Beijing and Taiyuan.Besides private vehicle CO2emission,GDP also plays an important role in UPT CO2emissions of Chengdu,Shanghai,Guangzhou,and Urumqi.Contributions of private vehicle CO2 emission and GDP to UPT CO2 emission are almost same in Xi'an.

CO2 and SO2 emission characteristics of the whole process industry chain of coal processing and utilization in China

The total coal consumption in China is on the rise.The characteristics of CO2 and SO2 emissions in the whole process of coal processing and utilization in China are worthy of study.Based on the five links of the whole process of coal production and utilization,including coal production,raw coal processing,logistics and transportation,conversion and utilization and resource utilization,this paper summarized and analyzed the energy consumption and pollutant emission sources of these five links,combined with the US Environmental Protection Agency’s AP-42 method and IPCC method,to calculate total pollutant discharge and emission factors,where the emission factors were corrected by conversion efficiency.At the same time,uncertainty analysis is performed about CO2 and SO2 emissions.The results showed that CO2 emissions were 3.657 billion tons,and emission reductions were 61 million tons,and SO2 emissions were 4,844,500 tons,and emission reductions were 10.3595 million tons in 2015.

Effect of Partial Root-Zone Irrigating Deuterium Oxide on the Properties of Water Transportation and Distribution in Young Apple Trees

Partial root-zone irrigation （PRI） has been proved to be an optimal water-saving irrigation technology, however, few studies were done on water transportation and distribution under PRI. The present study was performed to investigate the water transportation and distribution among the wet and dry root-zones and the shoot using deuterium water （D2O） in 1/4 root-zone PRI experiment. It also aimed to determine and analyze the D2O relative abundance within different types of roots and shoots. The results indicated that water could be transported from roots in wet root-zone to roots in dry root-zone and shoots within 2 h after irrigation. Water transportation in roots of wet-zone was carried out by absorbing root, 1-2 mm root, 2-5 mm root, and〉5 mm root progressively, while through a reverse process in three dry root-zones. In shoots, water was transported to trunk, central trunk, annual branches, shoot and leaf progressively. Thus in the young apple trees subjected to PRI, water was distributed ifrst in the roots, including the roots in the wet and dry root-zones, to satisfy the water need of roots itself, and then transported to the shoot within hours of irrigation.

Experimental study on the effect of H2S and SO2 on high temperature corrosion of 12Cr1MoV

Aiming at the high temperature corrosion in a coal-fired boiler,the effect of H2S and SO2 on the corrosion of 12 CrlMoV under the water wall condition has been investigated by experiments.The results indicate that H2 S can promote the corrosion significantly,and the coarse porous oxide film formed cannot stop the progress of corrosion.While SO2 presents little effect on the corrosion.The main composition of the surface of 12 CrlMoV corrosion products is Fe2 O3.With H2S in the atmosphere,the corrosion gradually develops into deeper layers by forming FeS,FeO and Fe2 O3 alternately.The corrosion rate is doubled for every 50℃ inerease in temperature at 400-500℃.

γ-MnO2 nanorods/graphene composite as efficient cathode for advanced rechargeable aqueous zinc-ion battery

Aqueous Zn//MnO2 batteries are emerging as promising large-scale energy storage devices owing to their cost-effectiveness,high safety,high output voltage,and energy density.However,the MnO2 cathode suffers from intrinsically poor rate performance and rapid capacity deterioration.Here,we remove the roadblock by compositing MnO2 nanorods with highly conductive graphene,which remarkably enhances the electrochemical properties of the MnO2 cathode.Benefiting from the boosted electric conductivity and ion diffusion rate as well as the structural protection of graphene,the Zn//MnO2-graphene battery presents an admirable capacity of 301 mAh g^-1 at 0.5 A g^-1,corresponding to a high energy density of 411.6 Wh kg^-1.Even at a high current density of 10 A g^-1,a decent capacity of 95.8 mAh g^-1 is still obtained,manifesting its excellent rate property.Furthermore,an impressive power density of 15 kW kg^-1 is achieved by the Zn//MnO2-graphene battery.

A study on simultaneous removal of NO and SO2 by using sodium persulfate aqueous scrubbing

Nitric oxide(NO) removal and sulfur dioxide(SO_2) removal by sodium persulfate(Na_2S_2O_8) were studied in a Bubble Column Reactor. The proposed reaction pathways of NO and SO_2 removal are discussed. The effects of temperatures(35–90 °C), Na_2S_2O_8(0.05–0.5 mol·L^(-1)), Fe SO4(0.5–5.0 m mol·L^(-1)) and H_2O_2(0.25 mol·L^(-1))on NO and SO_2 removal were investigated. The results indicated that increased persulfate concentration led to increase in NO removal at various temperatures. SO_2 was almost completely removed in the temperature range of 55–85 °C. Fe^(2+)accelerated persulfate activation and enhanced NO removal efficiency. At 0.2 mol·L^(-1) Na_2S_2O_8 and 0.5–1.0 mmol·L^(-1) Fe^(2+), NO removal of 93.5%–99% was obtained at 75–90 °C, SO_2 removal was higher than 99% at all temperatures. The addition of 0.25 mol·L^(-1) H_2O_2 into 0.2 mol·L^(-1) Na_2S_2O_8 solution promoted NO removal efficiency apparently until utterly decomposition of H2 O2, the SO_2 removal was as high as98.4% separately at 35 °C and 80 °C.

Ultra-lightweight Ti3C2Tx MXene modified separator for Li–S batteries:Thickness regulation enabled polysulfide inhibition and lithium ion transportation

The practical application of lithium–sulfur(Li–S)batteries is limited by the easy dissolution of polysulfides in the electrolyte,resulting in the lithium polysulfide(LPS)shuttle effect.Several two-dimensional(2D)materials with abundant active binding sites and high surface-to-volume ratios have been developed to prepare functional separators that suppress the diffusion of polysulfides.However,the influence of modified layer thickness on Li+transport has not been considered.Herein,we synthesized individual and multilayered 2D Ti3C2Tx MXene nanosheets and used them to fabricate a series of Ti3C2Tx-PP modified separators.The separators had mass loadings ranging from 0.16 to 0.016 mg cm-2,which is the lowest value reported for 2D materials to the best of our knowledge.The corresponding reductions in thickness ranged from 1.2μm to 100 nm.LPS shuttling was effectively suppressed,even at the lowest mass loading of 0.016 mg cm-2.Suppression was due to the strong interaction between LPS intermediates and Ti atoms and hydroxyl functional groups on the separator surface.The lithium-ion diffusion coefficient increased with the reduction of Ti3C2Tx layers on the separator.Superior cycling stability and rate performance were attained when the separator with a Ti3C2Tx-PP mass loading of 0.016 mg cm-2 was incorporated into a Li–S battery.Carbon nanotubes(CNTs)were introduced into the separators to further improve the electrical and Li+ionic conductivity in the cross-plane direction of the 2D Ti3C2Txlayers.With the ultralightweight Ti3C2Tx/CNTs modified PP separator,the cell maintained a capacity of 640 m Ah g-1after 200cycles at 1C with a capacity decay of only 0.079%per cycle.

Electrochemical CO2 reduction over nitrogen-doped SnO2 crystal surfaces

Crystal planes of a catalyst play crucial role in determining the electrocatalytic performance for CO2 reduction.The catalyst SnO2 can convert CO2 molecules into valuable formic acid(HCOOH).Incorporating heteroatom N into SnO2 further improves its catalytic activity.To understand the mechanism and realize a highly efficient CO2-to-HCOOH conversion,we used density functional theory(DFT)to calculate the free energy of CO2 reduction reactions(CO2RR)on different crystal planes of N-doped SnO2(N-SnO2).The results indicate that N-SnO2 lowered the activation energy of intermediates leading to a better catalytic performance than pure SnO2.We also discovered that the N-Sn O2 (211)plane possesses the most suitable free energy during the reduction process,exhibiting the best catalytic ability for the CO2-to-HCOOH conversion.The intermediate of CO2RR on N-SnO2 is HCOO*or COOH* instead of OCHO*.These results may provide useful insights into the mechanism of CO2RR,and promote the development of heteroatomdoped catalyst for efficient CO2RR.

Novel Insights into Energy Storage Mechanism of Aqueous Rechargeable Zn/MnO2 Batteries with Participation of Mn2+

Aqueous rechargeable Zn/MnO2 zinc-ion batteries(ZIBs)are reviving recently due to their low cost,non-toxicity,and natural abundance.However,their energy storage mechanism remains controversial due to their complicated electrochemical reactions.Meanwhile,to achieve satisfactory cyclic stability and rate performance of the Zn/MnO2 ZIBs,Mn2+ is introduced in the electrolyte(e.g.,ZnSO4 solution),which leads to more complicated reactions inside the ZIBs systems.Herein,based on comprehensive analysis methods including electrochemical analysis and Pourbaix diagram,we provide novel insights into the energy storage mechanism of Zn/MnO2 batteries in the presence of Mn2+.A complex series of electrochemical reactions with the coparticipation of Zn2+,H+,Mn2+,SO42-,and OH-were revealed.During the first discharge process,co-insertion of Zn2+ and H+ promotes the transformation of MnO2 into ZnxMnO4,MnOOH,and Mn2O3,accompanying with increased electrolyte pH and the formation of ZnSO4·3 Zn(OH)2-5 H2O.During the subsequent charge process,ZnxMnO4,MnOOH,and Mn2O3 revert to a-MnO2 with the extraction of Zn2+ and H+,while ZnSO4·3Zn(OH)2·5H2O reacts with Mn2+ to form ZnMn3O7·3 H2O.In the following charge/discharge processes,besides aforementioned electrochemical reactions,Zn2+ reversibly insert into/extract from α-MnO2,ZnxMnO4,and ZnMn3O7·3H2O hosts;ZnSO4·3Zn(OH)2·5 H2O,Zn2Mn3O8,and ZnMn2O4 convert mutually with the participation of Mn2+.This work is believed to provide theoretical guidance for further research on high-performance ZIBs.

Emerging CoMn-LDH@MnO2 electrode materials assembled using nanosheets for flexible and foldable energy storage devices

CoMn layered double hydroxides(CoMn-LDH)are promising electrode materials for supercapacitors because of their excellent cyclic stability.However,they possess relatively low capacitances.In this work,hybrid CoMn-LDH@MnO2 products grown on Ni foams were obtained through a facile hydrothermal method.The as-synthesized samples employed as electrodes deliver a specific capacitance of 2325.01 F g^-1 at 1 A g^-1.An assembled asymmetric supercapacitor using these products as positive electrodes shows a maximum energy density of 59.73 W h kg^-1 at 1000.09 W kg^-1.The prominent electrochemical performance of the as-prepared electrodes could be attributes to hierarchical structures.These findings suggest that hybrid structures might be potential alternatives for future flexible energy storage devices.