Transforming liquid flow fuel cells to controllable reactors for highlyefficient oxidation of 5-hydroxymethylfurfural to 2, 5-furandicarboxylic acid at low temperature

Highly-efficient oxidation of 5-hydroxymethylfurtural(HMF) to 2,5-furandicarboxylic acid(FDCA) at low temperature with air as the oxidant is still challenging.Herein,inspired by the respirato ry electron transport chain(ETC) of living cells mediated by electron carriers,we constructed artificial ETCs and transformed liquid flow fuel cells(LFFCs) to flexible reactors for efficient oxidation of HMF to produce FDCA under mild conditions.This LFFC reactor employed an electrodeposition modified nickel foam as an anode to promote HMF oxidation and(VO_(2))_(2)SO_(4) as a cathode electron carrier to facilitate the electron transfer to air.The reaction rate could be easily controlled by selecting the anode catalyst,adjusting the external loading and changing the cathodic electron carrier or oxidants.A maximal power density of 44.9 mW cm^(-2) at room temperature was achieved,while for FDCA production,short-circuit condition was preferred to achieve quick transfer of electrons.For a single batch operation with 0.1 M initial HMF,FDCA yield reached 97.1%.By fed-batch operation,FDCA concentration reached 144.5 g L^(-1) with a total yield of 96%.Ni^(2+)/Ni^(3+) redox couple was the active species mediating the electron transfer,while both experimental and DFT calculation results indicated that HMFCA pathway was the preferred reaction mechanism.

Electrochemical reduction of carbon dioxide to produce formic acid coupled with oxidative conversion of biomass

Electrochemical reduction of CO_(2)(CO_(2)RR)has become a research hot spot in recent years in the context of carbon neutrality.HCOOH is one of the most promising products obtained by electrochemical reduction of CO_(2) due to its high energy value as estimated by market price per energy unit and wide application in chemical industry.Biomass is the most abundant renewable resource in the natural world.Coupling biomass oxidative conversion with CO_(2)RR driven by renewable electricity would well achieve carbon negativity.In this work,we comprehensively reviewed the current research progress on CO_(2)RR to produce HCOOH and coupled system for conversion of biomass and its derivatives to produce value-added products.Sn-and Bi-based electrocatalysts are discussed for CO_(2)RR with regards to the structure of the catalyst and reaction mechanisms.Electro-oxidation reactions of biomass derived sugars,alcohols,furan aldehydes and even polymeric components of lignocellulose were reviewed as alternatives to replace oxygen evolution reaction(OER)in the conventional electrolysis process.It was recommended that to further improve the efficiency of the coupled system,future work should be focused on the development of more efficient and stable catalysts,careful design of the electrolytic cells for improving the mass transfer and development of environment-friendly processes for recovering the formed formate and biomass oxidation products.

Promoting and controlling electron transfer of furfural oxidation efficiently harvest electricity,furoic acid,hydrogen gas and hydrogen peroxide

Conventional chemical oxidation of aldehydes such as furfural to corresponding acids by molecular oxygen usually needs high pressure to increase the solubility of oxygen in aqueous phase,while electrochemical oxidation needs input of external electric energy.Herein,we developed a liquid flow fuel cell(LFFC)system to achieve oxidation of furfural in anode for furoic acid production with co-production of hydrogen gas.By controlling the electron transfer in cathode for reduction of oxygen,efficient generation of electricity or production of H_(2)O_(2)were achieved.Metal oxides especially Ag_(2)O have been screened as the efficient catalyst to promote the oxidation of aldehydes,while liquid redox couples were used for promoting the kinetics of oxygen reduction.A novel alkaline-acidic asymmetric design was also used for anolyte and catholyte,respectively,to promote the efficiency of electron transfer.Such an LFFC system achieves efficient conversion of chemical energy of aldehyde oxidation to electric energy and makes full use the transferred electrons for high-value added products without input of external energy.With(VO_(2))_(2)SO_(4)as the electron carrier in catholyte for four-electron reduction of oxygen,the peak output power density(Pmax)at room temperature reached 261 mW/cm^(2)with furoic acid and H_(2)yields of 90%and 0.10 mol/mol furfural,respectively.With anthraquinone-2-sulfonate(AQS)as the cathodic electron carrier,Pmaxof 60 mW/cm^(2)and furoic acid,H_(2)and H_(2)O_(2)yields of 0.88,0.15 and 0.41 mol/mol furfural were achieved,respectively.A new reaction mechanism on furfural oxidation on Ag_(2)O anode was proposed,referring to one-electron and two-electron reaction pathways depending on the fate of adsorbed hydrogen atom transferred from furfural aldehyde group.

Lignocellulosic biomass as sustainable feedstock and materials for power generation and energy storage

Lignocellulosic biomass has attracted great interest in recent years for energy production due to its renewability and carbon-neutral nature.There are various ways to convert lignocellulose to gaseous,liquid and solid fuels via thermochemical,chemical or biological approaches.Typical biomass derived fuels include syngas,bio-gas,bio-oil,bioethanol and biochar,all of which could be used as fuels for furnace,engine,turbine or fuel cells.Direct biomass fuel cells mediated by various electron carriers provide a new direction of lignocellulose conversion.Various metal and non-metal based carriers have been screened for mediating the electron transfer from biomass to oxygen thus generating electricity.The power density of direct biomass fuel cells can be over 100 mW cm^(-2),which shows promise for practical applications.Lignocellulose and its isolated components,primarily cellulose and lignin,have also been paid considerable attention as sustainable carbonaceous materials for preparation of electrodes for supercapacitors,lithium-ion batteries and lithium-sulfur batteries.In this paper,we have provided a state-of-the-art review on the research progress of lignocellulosic biomass as feedstock and materials for power generation and energy storage focusing on the chemistry aspects of the processes.It was recommended that process integration should be performed to reduce the cost for thermochemical and biological conversion of lignocellulose to biofuels,while efforts should be made to increase efficiency and improve the properties for biomass fuelled fuel cells and biomass derived electrodes for energy storage.

Coupling biomass pretreatment for enzymatic hydrolysis and direct biomass-to-electricity conversion with molybdovanadophosphoric heteropolyacids as anode electron transfer carriers

Owing to their acidity,oxidizing ability and redox reversibility,molybdovanadophosphoric heteropolyacids(H_(n+3)PMo_(12-n)VnO40,abbreviated as PMo_(12-n)Vn) were employed as electron transfer carriers for coupling biomass pretreatment for enzymatic hydrolysis and direct biomass-to-electricity conversion.In this novel coupled process,PMo_(12-n)Vn pretreatment that causes deconstruction of cell wall structure with PMo_(12-n)Vn being simultaneously reduced can be considered as the "charging" process.The reduced PMo_(12-n)Vn are further re-oxidized with release of electrons in a liquid flow fuel cell(LFFC) to generate electricity is the "discharging" process.Several Keggin-type PMo_(12-n)Vn with different degree of vanadium substitution(DSV, namely n) were prepared.Compared to Keggin-type phosphomolybdic acid(PMo_(12)),PMo_(12-n)Vn(n=1-6) showed higher oxidizing ability but poorer redox reversibility.The cellulose enzymatic digestibility of PMo_(12-n)Vn pretreated wheat straw generally decreased with increase in DSV, but xylan enzymatic digestibility generally increased with DSV.PMo_(12) pretreatment of wheat straw at 120℃ obtained the highest enzymatic glucan conversion(EGC) reaching 95%,followed by PMo11V1 pretreatment(85%).Discharging of the reduced heteropolyacids in LFFC showed that vanadium substitution could improve the maximum output power density(Pmax).The highest Pmax was obtained by PMo9 V3(44.7 mW/cm^(2)) when FeCl_(3) was used as a cathode electron carrier,while PMo_(12) achieved the lowest Pmax(27.4 mW/cm^(2)).All the heteropolyacids showed good electrode Faraday efficiency(>95%) and cell discharging efficiency(>93%).The energy efficiency of the coupled process based on the heat values of the products and generated electric energy was in the range of 18%-25% depending on DSV.PMo_(12) and PMo11V1 seem to be the most suitable heteropolyacids to mediate the coupled process.

Distribution of birds in the high-altitude area of Mount Everest

INTRODUCTION The Himalayas includes the world’s highest peak,Mount Everest(8848 m),and the altitude gradient of the southern slope of the mountain range changes rapidly,from Mount Everest to 100 km south,with the habitat shifting from glaciers to tropical rain forests at altitudes below 1000 m.This area is a global hotspot for bird distribution(Orme et al.2005),and the area is home to one of the highest concentrations of threatened birds in Asia.(Acharya&Vijayan 2010).Bird diversity research in this area has revealed that the eastern Himalaya mountain range,south slopes,and mid-lower altitude areas have higher levels of bird diversity than the western Himalaya mountain range,north slopes,and high-altitude areas,respectively(Acharya et al.2010,2011;Price et al.2011;Wang et al.2013;Romanov et al.2016).In addition,the adaptability of birds to high-altitude areas,such as the enhancement of the oxygen transport capacity of the Barheaded Goose(Meir&Milsom 2013)and changes in the flight characteristics of vultures(Sherub et al.2016)have also been investigated.However,most of these studies were carried out at altitudes below 5000 m.For the mountain range with the highest peak,at 8848 m,there are very few studies on the birds in large areas above the snow line,and bird data at very high altitudes mainly come from the sporadic records of early climbers(Swan 1961,1970).

Understanding the role of interface in advanced semiconductor nanostructure and its interplay with wave function overlap

As the proportion of interfaces increases rapidly in nanomaterials,properties and quality of interfaces hugely impact the performance of advanced semiconductors.Here,the effect of interfaces is explored by comparatively studying two InAs/AlSb superlattices with and without the thin InAsSb layers inserted inside each InAs layers.Through strain mapping,it indicates that the addition of interfaces leads to an increase of local strain both near interfaces and inside layers.Meantime,owing to the creation of hole potential wells within the original electron wells,the charge distribution undergoes an extra electron-hole alternating arrangement in the structure with inserted layers than the uninserted counterpart.Such a feature is verified to enhance electron-hole wave function overlap by theoretical simulations,which is a must for better optical performance.Furthermore,with an elaborate design of the inserted layers,the wave function overlap could be boosted without sacrificing other key device performances.

Uniform wurtzite MnSe nanocrystals with surface-dependent magnetic behavior

锰硒化物(MnSe ) 作为一个重要磁性的半导体拥有唯一的磁性，但是 MnSe nanocrystals 的合成和性质是因为无能，与另外的半导体 nanocrystals 相比开发获得高质量的 MnSe 的更少，特别在亚稳的 wurtzite 结构。这里，我们成功地经由负担得起一致水晶尺寸的一条胶体的途径制作了 wurtzite MnSe nanocrystals 并且定制形状。胺表面活化剂的选择有约束力的力量是在形状控制和形状进化的决定因素。如果在反应解决方案的 oleylamine 的部分被 trioctylamine 代替，子弹形状能被转变成梭形状，并且四足动物形状的 nanocrystals 能在 trioctylamine 系统被形成。三维(3D ) 塑造子弹的 nanorods 的结构被先进传播电子显微镜(TEM ) 表明了 3D 断层摄影术技术。高分辨率的 TEM (HRTEM ) 和电子精力损失光谱学(鳗) 显示出那平面缺点的结构象叠差错和 twinning 沿着那样[001 ] 方向在子弹形状的生长期间产生。根据小心的 HRTEM 观察，我们为 wurtzite MnSe nanotetrapods 的形成建议 quadra 双胞胎核心生长机制。而且，由于他们的 noncompensated，表面旋转的 wurtzite MnSe nanocrystals 表演 lowtemperature 表面纺纱眼镜行为和堵住的温度与增加 nanocrystals 的表面区域 / 卷比率从 8.4 K 增加到 18.5 K。我们的结果提供 wurtzite MnSe nanocrystals 的系统的研究。