Ga_(2)O_(3) is considered a potential anode material for next-generation lithium-ion batteries due to its high theoretical capacity and unique self-healing capability.To develop a novel preparation method and in-depth...Ga_(2)O_(3) is considered a potential anode material for next-generation lithium-ion batteries due to its high theoretical capacity and unique self-healing capability.To develop a novel preparation method and in-depth understanding of the electrochemical reaction mechanism of Ga_(2)O_(3),a brand-new liquid-liquid dealloying strategy was exploited to construct porous α-Ga_(2)O_(3) nanowire networks.Profiting from the well-designed porous structure,the material exhibits impressive cycling stability of a reversible capacity of 603.9 mA·h/g after 200 cycles at 1000 mA/g and a capacity retention of 125.2 mA·h/g after 100 cycles at 0.5C when assembling to Ga_(2)O_(3)//LiFePO_(4) full cells.The lithiation/delithiation reaction mechanism of the porous Ga_(2)O_(3) anodes is further revealed by ex-situ Raman,XRD,TEM measurements,and density functional theoretical(DFT)calculations,which establishes a correlation between the electrochemical performance and the phase transition fromα-Ga_(2)O_(3) to β-Ga_(2)O_(3) during cycling.展开更多
Broadband transparent films play a pivotal role in various applications such as lenses and solar cells,particularly porous structured transparent films exhibit significant potential.This study investigates a porous Si...Broadband transparent films play a pivotal role in various applications such as lenses and solar cells,particularly porous structured transparent films exhibit significant potential.This study investigates a porous SiO_(2) refractive index gradient anti-reflective film prepared by atomic layer deposition(ALD).A porous SiO_(2) film with gradual porosity was obtained by phosphoric acid etching of Al_(2)O_(3)/SiO_(2) multilayers with gradient Al2O3 ratios,achieving a gradual decrease in refractive index from the substrate to the surface.The film exhibited an average transmittance as high as 97.8%within the wavelength range from 320 nm to 1200 nm.The environmental adaptability was further enhanced by surface modification using rare earth oxide(REO)La_(2)O_(3),resulting in formation of a lotus leaf-like structure and achieving a water contact angle of 100.0°.These data proved that the modification significantly improved hydrophobic self-cleaning capability while maintaining exceptional transparency of the film.The surface structure of the modified film remained undamaged even after undergoing wipe testing,demonstrating its excellent surface durability.展开更多
A new adsorbent was successfully prepared by hydrothermal treatment and chemical activation through coal gasification fine slag(CGFS)and blue algae(BA)as raw materials and used for CO_(2)capture.The CO_(2)chemisorptio...A new adsorbent was successfully prepared by hydrothermal treatment and chemical activation through coal gasification fine slag(CGFS)and blue algae(BA)as raw materials and used for CO_(2)capture.The CO_(2)chemisorption capacity of the adsorbent was further enhanced by taking advantage of the nitrogenous bases contained in the BA.In the hydrothermal process,the addition of BA significantly increased the content of pyrrole nitrogen in the adsorbent.In the activation process,pyrrole nitrogen gradually changed into pyridine nitrogen and graphite nitrogen.Increased BA addition result in a higher specific surface area and microporosity of the adsorbent.The CO_(2)adsorption performance test proved that the CGFS-50%-CA sample has the strongest CO_(2)adsorption capacity at low temperature,up to 15.59 cm^(3)/g,which is mainly through physical adsorption,and the CGFS-10%-CA sample has the strongest CO_(2)adsorption capacity at high temperature,up to 7.31 cm^(3)/g,which is mainly through chemical adsorption.CO_(2)uptake of the CGFS-10%-CA sample was well maintained after 10 cycles,with regeneration efficiencies above 99%.The results indicate that the novel adsorbents with coexistence of physical and chemical adsorption have great potential for CO_(2)adsorption applications.展开更多
The performance of supercapacitors can be improved by strategically designing 2D MXene-based electrodes with excellent electrochemical properties. However, several challenges remain in developing hybrid materials base...The performance of supercapacitors can be improved by strategically designing 2D MXene-based electrodes with excellent electrochemical properties. However, several challenges remain in developing hybrid materials based on 2D MXenes due to restacking, which hinders energy storage performance. In this work, we successfully synthesized a 2D MXene/Ni-Co phosphide (MX/NCP) hybrid material for supercapacitors via a facile hydrothermal reaction followed by phosphorization. The optimized MX/NCP positive electrode showed good energy storage performance with a specific capacitance of 1754.0 F g^(-1) at 3 mA cm^(-2) in a three-electrode configuration. The synergistic effect of MXene and Ni-Co phosphide has contributed towards the enhanced charge storage performance. Furthermore, an asymmetric supercapacitor (ASC) fabricated with MX/NCP and porous nanocarbon (PNC) delivered a maximum energy density of 54.3 Wh kg^(-1) at a power density of 565.6 W kg^(-1) with a cycling stability of 93.8 % after 10,000 cycles. To evaluate the practical versatility of the ASC, a planar device was successfully fabricated making MX/NCP a promising electrode material in next-generation wearable and flexible supercapacitors.展开更多
Porous liquid-conducting micro-heat exchangers have garnered considerable attention for their role in efficient heat dissipation in small electronic devices.This demand highlights the need for advanced mathematical mo...Porous liquid-conducting micro-heat exchangers have garnered considerable attention for their role in efficient heat dissipation in small electronic devices.This demand highlights the need for advanced mathematical models to optimize the selection of mixed heat exchange media and equipment design.A capillary bundle evaporation model for porous liquid-conducting media was developed based on the conjugate mass transfer evaporation rate prediction model of a single capillary tube,supplemented by mercury injection experimental data.Theoretical and experimental comparisons were conducted using 1,2-propanediol-glycerol(PG-VG)mixtures at molar ratios of 1:9,3:7,5:5,and 7:3 at 120,150,and 180℃.The Jouyban-Acree model was implemented to enhance the evaporation rate predictions.For the 7:3 PG-VG mixture at 180℃under the experimental conditions of the thermal medium,the model's error reduced from 16.75%to 10.84%post-correction.Overall,the mean relative error decreased from 11.76%to 5.98%after correction.展开更多
Leveraging the interplay between the metal component and the supporting material represents a cornerstone strategy for augmenting electrocatalytic efficiency,e.g.,electrocatalytic CO_(2)reduction reaction(CO_(2)RR).He...Leveraging the interplay between the metal component and the supporting material represents a cornerstone strategy for augmenting electrocatalytic efficiency,e.g.,electrocatalytic CO_(2)reduction reaction(CO_(2)RR).Herein,we employ freestanding porous carbon fibers(PCNF)as an efficacious and stable support for the uniformly distributed SnO_(2)nanoparticles(SnO_(2)PCNF),thereby capitalizing on the synergistic support effect that arises from their strong interaction.On one hand,the interaction between the SnO_(2)nanoparticles and the carbon support optimizes the electronic configuration of the active centers.This interaction leads to a noteworthy shift of the d-band center toward stronger intermediate adsorption energy,consequently lowering the energy barrier associated with CO_(2)reduction.As a result,the Sn O_(2)PCNF realizes a remarkable CO_(2)RR performance with excellent selectivity towards formate(98.1%).On the other hand,the porous carbon fibers enable the uniform and stable dispersion of SnO_(2)nanoparticles,and this superior porous structure of carbon supports can also facilitate the exposure of the SnO_(2)nanoparticles on the reaction interface to a great extent.Consequently,adequate contact between active sites,reactants,and electrolytes can significantly increase the metal utilization,eventually bringing forth a remarkable7.09 A/mg mass activity.This work might provide a useful idea for improving the utilization rate of metals in numerous electrocatalytic reactions.展开更多
It is well known that adsorbent material is the key to determine the CO_(2)adsorption performance.Herein,ZIF-8 derived porous carbon(ZIF-8-C)is anchored into the framework of a novel composite aerogel(ZCPx),which util...It is well known that adsorbent material is the key to determine the CO_(2)adsorption performance.Herein,ZIF-8 derived porous carbon(ZIF-8-C)is anchored into the framework of a novel composite aerogel(ZCPx),which utilizes chitosan(CS)and polyvinyl alcohol(PVA)as raw materials.By controlling the ratio of ZIF-8-C,the developed hierarchical porous structures combine the advantages of micropores,mesopores,and macropores.Besides,the ligand material of ZIF-8-C and the amino group from CS are two sources of the high nitrogen content of ZCPx.The optimized sample ZCP4 shows a high nitrogen content of 6.78%,which can create more active centers and supply basic sites,thereby enhancing the CO_(2)adsorption capacity.Moreover,ZC P4 composite aerogel presents a CO_(2)adsorption capacity of2.26 mmol·g^(-1)(298 K,0.1 MPa)and CO_(2)/N_(2)selectivity(S_(CO_(2))/N_(2))can reach 20.02,and the dynamic breakthrough experiment is performed to confirm the feasibility of CO_(2)/N_(2)actual separation performance,proving that the composite aerogel is potential candidates for CO_(2)adsorption.展开更多
CO_(2)enhanced oil recovery plays an important role in carbon storage and utilization.However,the incomplete understanding of the underlying microscopic convection–diffusion mechanisms in complex pore structures has ...CO_(2)enhanced oil recovery plays an important role in carbon storage and utilization.However,the incomplete understanding of the underlying microscopic convection–diffusion mechanisms in complex pore structures has constrained the broader industrial application of CO_(2)geo-sequestration.This work develops a pore-scale numerical model considering molecular convection–diffusion to investigate CO_(2)-oil miscible displacement in two-and three-dimensional porous structures of conglomerate rocks.The effects of CO_(2)injection rates and pore structure properties on convection–diffusion are analyzed.By reconstructing the distribution of unexploited pores,the CO_(2)sweep efficiency is quantitatively evaluated.Furthermore,a sequestration factor is proposed to evaluate the CO_(2)storage capacity during miscible displacement.Convection significantly enhances the CO_(2)mass fraction in fractures with high flow rates.Subsequently,CO_(2)gradually diffuses into matrix pores without velocity distribution.Both convection and diffusion contribute to improving CO_(2)displacement efficiency.Diffusion facilitates the dissolution of CO_(2)into oil within small-diameter pores,and convection effectively mobilizes oil in large pore bodies.Developed and homogeneous pore structures enhance CO_(2)displacement efficiency,whereas CO_(2)flows along the main flow channels in heterogeneous pore structures,resulting in lower displacement efficiency.Diffusion plays a crucial role in CO_(2)storage within porous media.At low injection rates,dissolved CO_(2)is trapped in poorly connected and blind-end pores.The injection rate is negatively correlated with the sequestration factor.展开更多
Zn-CO_(2)batteries(ZCBs)are promising for CO_(2)conversion and electric energy release.However,the ZCBs couple the electrochemical CO_(2)reduction(ECO_(2)R)with the oxygen evolution reaction and competitive hydrogen e...Zn-CO_(2)batteries(ZCBs)are promising for CO_(2)conversion and electric energy release.However,the ZCBs couple the electrochemical CO_(2)reduction(ECO_(2)R)with the oxygen evolution reaction and competitive hydrogen evolution reaction,which normally causes ultrahigh charge voltage and CO_(2)conversion efficiency attenuation,thereby resulting in~90%total power consumption.Herein,isolated FeN_(3)sites encapsulated in hierarchical porous carbon nanoboxes(Fe-HPCN,derived from the thermal activation process of ferrocene and polydopamine-coated cubic ZIF-8)were proposed for hydrazine-assisted rechargeable ZCBs based on ECO_(2)R(discharging process:CO_(2)+2H+→CO+H_(2)O)and hydrazine oxidation reaction(HzOR,charging process:N_(2)H_(4)+4OH−→N_(2)+4H_(2)O+4e^(−)).The isolated FeN_(3)endows the HzOR with a lower overpotential and boosts the ECO_(2)R with a 96%CO Faraday efficiency(FECO).Benefitting from the bifunctional ECO_(2)R and HzOR catalytic activities,the homemade hydrazine-assisted rechargeable ZCBs assembled with the Fe-HPCN air cathode exhibited an ultralow charge voltage(decreasing by~1.84 V),excellent CO selectivity(FECO close to 100%),and high 89%energy efficiency.In situ infrared spectroscopy confirmed that Fe-HPCN can generate rate-determining*N_(2)and*CO intermediates during HzOR and ECO_(2)R.This paper proposes FeN_(3)centers for bifunctional ECO_(2)R/HzOR performance and further presents the pioneering achievements of ECO_(2)R and HzOR for hydrazine-assisted rechargeable ZCBs.展开更多
MXene is an emerging class of two-dimensional(2D)layered transition metal carbides or nitrides.Due to the highly tunable components and surface functional groups,it holds great potential in electrocatalytic hydrogen e...MXene is an emerging class of two-dimensional(2D)layered transition metal carbides or nitrides.Due to the highly tunable components and surface functional groups,it holds great potential in electrocatalytic hydrogen evolution reaction(HER).However,MXene nanosheet suffers from a strong tendency to restack and a lack of active edge sites.In this work,the porous Ti_(3)C_(2)T_(x)was synthesized by an oxidation and etching two-step strategy and then characterized by a series of spectroscopic techniques.The obtained porous Ti_(3)C_(2)T_(x)possesses a large number of in-plane pores.This not only creates abundant active edge sites but also enhances the mass transfer and increases the accessibility of the active sites.Compared with Ti_(3)C_(2)T_(x),in a 0.5 mol/L H_(2)SO_(4)electrolyte,the porous Ti_(3)C_(2)T_(x)shows a 65.6%higher electrochemical surface area(ECSA)(440 mF/cm^(2)),a 95.2%lower charge transfer resistance(12.8Ω),and a 69.8%lower Tafel slope(144 mV/dec),and thus exhibits lower overpotential with good stability at a current density of 10 mA/cm^(2).At the same time,the HER performance of the porous Ti_(3)C_(2)T_(x)can be further enhanced by near-infrared laser irradiation based on the localized surface plasmon resonance effect.展开更多
Chemical vapor deposition is the predominant method to prepare MgAl_(2)O_(4)fibers.However,it faces several challenges,including exorbitantly high reaction temperatures,substantial production costs,and relatively low ...Chemical vapor deposition is the predominant method to prepare MgAl_(2)O_(4)fibers.However,it faces several challenges,including exorbitantly high reaction temperatures,substantial production costs,and relatively low yields.In this study,porous MgAl_(2)O_(4)fibers were fabricated through a solid-state reaction method,utilizing MgSO_(4)·5Mg(OH)_(2)·3H_(2)O whiskers as templates,mixed with either aluminum sol orα-Al_(2)O_(3)micropowder.The impact of various parameters on the synthesis of porous MgAl_(2)O_(4)fibres was systematically investigated,including the heat treatment temperature(1000,1100 and 1300℃),the holding time(3 and 10 h)and the aluminum source(aluminum sol orα-Al_(2)O_(3)micropowder).The results reveal that:(1)in comparison with fibers synthesized usingα-Al_(2)O_(3)as the aluminum source,those prepared with aluminum sol exhibit a significantly higher generation amount of MgAl_(2)O_(4);(2)as the heat treatment temperature increases,Al_(2)O_(3)gradually reacts with MgO,continuously increasing the formation amount of porous MgAl_(2)O_(4)with small and uniformly distributed nanopores,and the synthesized porous MgAl_(2)O_(4)fibres have small and uniform nanopores;(3)the optimal synthesis process involves using aluminum sol as the aluminum source and firing at 1300℃ for 3 h.展开更多
Nanoconfinement is a promising approach to simultaneously enhance the thermodynamics,kinetics,and cycling stability of hydrogen storage materials.The introduction of supporting scaffolds usually causes a reduction in ...Nanoconfinement is a promising approach to simultaneously enhance the thermodynamics,kinetics,and cycling stability of hydrogen storage materials.The introduction of supporting scaffolds usually causes a reduction in the total hydrogen storage capacity due to“dead weight.”Here,we synthesize an optimized N-doped porous carbon(rN-pC)without heavy metal as supporting scaffold to confine Mg/MgH_(2) nanoparticles(Mg/MgH_(2)@rN-pC).rN-pC with 60 wt%loading capacity of Mg(denoted as 60 Mg@rN-pC)can adsorb and desorb 0.62 wt%H_(2) on the rN-pC scaffold.The nanoconfined MgH_(2) can be chemically dehydrided at 175℃,providing~3.59 wt%H_(2) with fast kinetics(fully dehydrogenated at 300℃ within 15 min).This study presents the first realization of nanoconfined Mg-based system with adsorption-active scaffolds.Besides,the nanoconfined MgH_(2) formation enthalpy is reduced to~68 kJ mol^(−1) H_(2) from~75 kJ mol^(−1) H_(2) for pure MgH_(2).The composite can be also compressed to nanostructured pellets,with volumetric H_(2) density reaching 33.4 g L^(−1) after 500 MPa compression pressure,which surpasses the 24 g L^(−1) volumetric capacity of 350 bar compressed H_(2).Our approach can be implemented to the design of hybrid H_(2) storage materials with enhanced capacity and desorption rate.展开更多
Both Ti foil and porous Ti were anodized in 0.5%HF and in ethylene glycol electrolyte containing 0.5%NH4F(mass fraction) separately. The results show that TiO2 nanotubes can be formed on Ti foil by both processes, whe...Both Ti foil and porous Ti were anodized in 0.5%HF and in ethylene glycol electrolyte containing 0.5%NH4F(mass fraction) separately. The results show that TiO2 nanotubes can be formed on Ti foil by both processes, whereas TiO2 nanotubes can be formed on porous Ti only in the second process. The overhigh current density led to the failure of the formation nanotubes on porous Ti in 0.5%HF electrolyte. TiO2 nanotubes were characterized by SEM and XRD. TiO2 nanotubes on porous Ti were thinner than those on Ti foil. Anatase was formed when TiO2 nanotubes were annealed at 400 °C and fully turned into rutile at 700 °C. To obtain good photodegradation, the optimal heat treatment temperature of TiO2 nanotubes was 450 °C. The porosity of the substrates influenced photodegradation properties. TiO2 nanotubes on porous Ti with 60% porosity had the best photodegradation.展开更多
A molten salt method was developed to prepare porous La1‐xSrxMn0.8Fe0.2O3 （0≤ x ≤ 0.6） micro‐spheres using hierarchical porous δ‐MnO2 microspheres as a template in eutectic NaNO3‐KNO3. X‐ray diffraction patt...A molten salt method was developed to prepare porous La1‐xSrxMn0.8Fe0.2O3 （0≤ x ≤ 0.6） micro‐spheres using hierarchical porous δ‐MnO2 microspheres as a template in eutectic NaNO3‐KNO3. X‐ray diffraction patterns showed that single phase LaMn0.8Fe0.2O3 with good crystallinity was syn‐thesized at 450℃ after 4 h. Transmission electron microscope images exhibited that the LaMn0.8Fe0.2O3 sample obtained at 450？？ after 4 h possessed a porous spherical morphology com‐posed of aggregated nanocrystallites. Field emission scanning electron microscope images indicated that the growth of the porous LaMn0.8Fe0.2O3 microspheres has two stages. SEM pictures showed that a higher calcination temperature than 450？？ had an adverse effect on the formation of a po‐rous spherical structure. The LaMn0.8Fe0.2O3 sample obtained at 450？？ after 4 h displayed a high BET surface area of 55.73 m2/g with a pore size of 9.38 nm. Fourier transform infrared spectra suggested that Sr2＋ions entered the A sites and induced a decrease of the binding energy between Mn and O. The CO conversion with the La1‐xSrxMn0.8Fe0.2O3 （0≤x≤0.6） samples indicated that the La0.4Sr0.6Mn0.8Fe0.2O3 sample had the best catalytic activity and stability. Further analysis by X‐ray photoelectron spectroscopy demonstrated that Sr2＋doping altered the content of Mn4＋ions, oxygen vacancies and adsorbed oxygen species on the surface, which affected the catalytic performance for CO oxidation.展开更多
The solution of H 2O 2 is proposed to post-treat thick porous silicon (PS) films.The prepared PS film as the cathode is applied about 10mA/cm 2 current in mixture of ethanol,HF,and H 2O 2 solutions,which is expec...The solution of H 2O 2 is proposed to post-treat thick porous silicon (PS) films.The prepared PS film as the cathode is applied about 10mA/cm 2 current in mixture of ethanol,HF,and H 2O 2 solutions,which is expected to improve the stability and the smoothness of the surface and the mechanical property of the thick porous silicon films.The microstructure of the PS thick films with thicknesse of 20μm and 70μm has been studied.The SEM images show significant improved smoothness on surface of PS films,and XRD spectra suggest the formation of oxide layer after post-treating in H 2O 2.展开更多
基金the Natural Science Foundation of Hebei Province,China(No.E2023202253)Hebei Higher Education Teaching Reform Research and Practice Project,China(No.2021GJJG050).
文摘Ga_(2)O_(3) is considered a potential anode material for next-generation lithium-ion batteries due to its high theoretical capacity and unique self-healing capability.To develop a novel preparation method and in-depth understanding of the electrochemical reaction mechanism of Ga_(2)O_(3),a brand-new liquid-liquid dealloying strategy was exploited to construct porous α-Ga_(2)O_(3) nanowire networks.Profiting from the well-designed porous structure,the material exhibits impressive cycling stability of a reversible capacity of 603.9 mA·h/g after 200 cycles at 1000 mA/g and a capacity retention of 125.2 mA·h/g after 100 cycles at 0.5C when assembling to Ga_(2)O_(3)//LiFePO_(4) full cells.The lithiation/delithiation reaction mechanism of the porous Ga_(2)O_(3) anodes is further revealed by ex-situ Raman,XRD,TEM measurements,and density functional theoretical(DFT)calculations,which establishes a correlation between the electrochemical performance and the phase transition fromα-Ga_(2)O_(3) to β-Ga_(2)O_(3) during cycling.
文摘Broadband transparent films play a pivotal role in various applications such as lenses and solar cells,particularly porous structured transparent films exhibit significant potential.This study investigates a porous SiO_(2) refractive index gradient anti-reflective film prepared by atomic layer deposition(ALD).A porous SiO_(2) film with gradual porosity was obtained by phosphoric acid etching of Al_(2)O_(3)/SiO_(2) multilayers with gradient Al2O3 ratios,achieving a gradual decrease in refractive index from the substrate to the surface.The film exhibited an average transmittance as high as 97.8%within the wavelength range from 320 nm to 1200 nm.The environmental adaptability was further enhanced by surface modification using rare earth oxide(REO)La_(2)O_(3),resulting in formation of a lotus leaf-like structure and achieving a water contact angle of 100.0°.These data proved that the modification significantly improved hydrophobic self-cleaning capability while maintaining exceptional transparency of the film.The surface structure of the modified film remained undamaged even after undergoing wipe testing,demonstrating its excellent surface durability.
基金supported by the National Natural Science Foundation of China(22168032)the National Key Research and Development Program of China(2023YFC3904302,2023YFB4103500)the Key Projects of Ning Dong Energy and Chemical Industry Base(2023NDKJXMLX022).
文摘A new adsorbent was successfully prepared by hydrothermal treatment and chemical activation through coal gasification fine slag(CGFS)and blue algae(BA)as raw materials and used for CO_(2)capture.The CO_(2)chemisorption capacity of the adsorbent was further enhanced by taking advantage of the nitrogenous bases contained in the BA.In the hydrothermal process,the addition of BA significantly increased the content of pyrrole nitrogen in the adsorbent.In the activation process,pyrrole nitrogen gradually changed into pyridine nitrogen and graphite nitrogen.Increased BA addition result in a higher specific surface area and microporosity of the adsorbent.The CO_(2)adsorption performance test proved that the CGFS-50%-CA sample has the strongest CO_(2)adsorption capacity at low temperature,up to 15.59 cm^(3)/g,which is mainly through physical adsorption,and the CGFS-10%-CA sample has the strongest CO_(2)adsorption capacity at high temperature,up to 7.31 cm^(3)/g,which is mainly through chemical adsorption.CO_(2)uptake of the CGFS-10%-CA sample was well maintained after 10 cycles,with regeneration efficiencies above 99%.The results indicate that the novel adsorbents with coexistence of physical and chemical adsorption have great potential for CO_(2)adsorption applications.
基金supported by the National Research Foundation of Korea(NRF)Grant funded by the Korean Govern-ment(MSIT)(Nos.RS-2023-00217581 and RS-2024-00345983).
文摘The performance of supercapacitors can be improved by strategically designing 2D MXene-based electrodes with excellent electrochemical properties. However, several challenges remain in developing hybrid materials based on 2D MXenes due to restacking, which hinders energy storage performance. In this work, we successfully synthesized a 2D MXene/Ni-Co phosphide (MX/NCP) hybrid material for supercapacitors via a facile hydrothermal reaction followed by phosphorization. The optimized MX/NCP positive electrode showed good energy storage performance with a specific capacitance of 1754.0 F g^(-1) at 3 mA cm^(-2) in a three-electrode configuration. The synergistic effect of MXene and Ni-Co phosphide has contributed towards the enhanced charge storage performance. Furthermore, an asymmetric supercapacitor (ASC) fabricated with MX/NCP and porous nanocarbon (PNC) delivered a maximum energy density of 54.3 Wh kg^(-1) at a power density of 565.6 W kg^(-1) with a cycling stability of 93.8 % after 10,000 cycles. To evaluate the practical versatility of the ASC, a planar device was successfully fabricated making MX/NCP a promising electrode material in next-generation wearable and flexible supercapacitors.
基金the funding support of National Natural Science Foundation of China(21978204)。
文摘Porous liquid-conducting micro-heat exchangers have garnered considerable attention for their role in efficient heat dissipation in small electronic devices.This demand highlights the need for advanced mathematical models to optimize the selection of mixed heat exchange media and equipment design.A capillary bundle evaporation model for porous liquid-conducting media was developed based on the conjugate mass transfer evaporation rate prediction model of a single capillary tube,supplemented by mercury injection experimental data.Theoretical and experimental comparisons were conducted using 1,2-propanediol-glycerol(PG-VG)mixtures at molar ratios of 1:9,3:7,5:5,and 7:3 at 120,150,and 180℃.The Jouyban-Acree model was implemented to enhance the evaporation rate predictions.For the 7:3 PG-VG mixture at 180℃under the experimental conditions of the thermal medium,the model's error reduced from 16.75%to 10.84%post-correction.Overall,the mean relative error decreased from 11.76%to 5.98%after correction.
基金supported by the National Natural Science Foundation of China(Nos.22172099,U21A20312)Guangdong Basic and Applied Basic Research Foundation(Nos.2023A1515012776,2022B1515120084)the Shenzhen Science and Technology Program(No.RCYX20200714114535052)。
文摘Leveraging the interplay between the metal component and the supporting material represents a cornerstone strategy for augmenting electrocatalytic efficiency,e.g.,electrocatalytic CO_(2)reduction reaction(CO_(2)RR).Herein,we employ freestanding porous carbon fibers(PCNF)as an efficacious and stable support for the uniformly distributed SnO_(2)nanoparticles(SnO_(2)PCNF),thereby capitalizing on the synergistic support effect that arises from their strong interaction.On one hand,the interaction between the SnO_(2)nanoparticles and the carbon support optimizes the electronic configuration of the active centers.This interaction leads to a noteworthy shift of the d-band center toward stronger intermediate adsorption energy,consequently lowering the energy barrier associated with CO_(2)reduction.As a result,the Sn O_(2)PCNF realizes a remarkable CO_(2)RR performance with excellent selectivity towards formate(98.1%).On the other hand,the porous carbon fibers enable the uniform and stable dispersion of SnO_(2)nanoparticles,and this superior porous structure of carbon supports can also facilitate the exposure of the SnO_(2)nanoparticles on the reaction interface to a great extent.Consequently,adequate contact between active sites,reactants,and electrolytes can significantly increase the metal utilization,eventually bringing forth a remarkable7.09 A/mg mass activity.This work might provide a useful idea for improving the utilization rate of metals in numerous electrocatalytic reactions.
基金supported by the Natural Science Foundation of Shandong Province(ZR2021ME124,ZR2023ME033)Science-Education-Industry Integration Innovation Pilot Project of Qilu University of Technology(2024GH09)+2 种基金Innovation Capacity Improvement Project of Small and Medium-Sized Technology-Based Enterprise of Shandong Province(2023TSGC0706,2022TSGC1022)Technological Innovation Projects of Shandong Province(202350700179,202351600213)Science and technology plan project of Shandong Railway Investment Holding Group(TTKJ2023-01)。
文摘It is well known that adsorbent material is the key to determine the CO_(2)adsorption performance.Herein,ZIF-8 derived porous carbon(ZIF-8-C)is anchored into the framework of a novel composite aerogel(ZCPx),which utilizes chitosan(CS)and polyvinyl alcohol(PVA)as raw materials.By controlling the ratio of ZIF-8-C,the developed hierarchical porous structures combine the advantages of micropores,mesopores,and macropores.Besides,the ligand material of ZIF-8-C and the amino group from CS are two sources of the high nitrogen content of ZCPx.The optimized sample ZCP4 shows a high nitrogen content of 6.78%,which can create more active centers and supply basic sites,thereby enhancing the CO_(2)adsorption capacity.Moreover,ZC P4 composite aerogel presents a CO_(2)adsorption capacity of2.26 mmol·g^(-1)(298 K,0.1 MPa)and CO_(2)/N_(2)selectivity(S_(CO_(2))/N_(2))can reach 20.02,and the dynamic breakthrough experiment is performed to confirm the feasibility of CO_(2)/N_(2)actual separation performance,proving that the composite aerogel is potential candidates for CO_(2)adsorption.
基金supported by National Natural Science Foundation of China(42172159,52404048)China Postdoctoral Science Foundation(2023M743870)+1 种基金Postdoctoral Fellowship Program of CPSF(GZB20230864)Frontier Interdisciplinary Exploration Research Program of China University of Petroleum,Beijing(2462024XKQY002).
文摘CO_(2)enhanced oil recovery plays an important role in carbon storage and utilization.However,the incomplete understanding of the underlying microscopic convection–diffusion mechanisms in complex pore structures has constrained the broader industrial application of CO_(2)geo-sequestration.This work develops a pore-scale numerical model considering molecular convection–diffusion to investigate CO_(2)-oil miscible displacement in two-and three-dimensional porous structures of conglomerate rocks.The effects of CO_(2)injection rates and pore structure properties on convection–diffusion are analyzed.By reconstructing the distribution of unexploited pores,the CO_(2)sweep efficiency is quantitatively evaluated.Furthermore,a sequestration factor is proposed to evaluate the CO_(2)storage capacity during miscible displacement.Convection significantly enhances the CO_(2)mass fraction in fractures with high flow rates.Subsequently,CO_(2)gradually diffuses into matrix pores without velocity distribution.Both convection and diffusion contribute to improving CO_(2)displacement efficiency.Diffusion facilitates the dissolution of CO_(2)into oil within small-diameter pores,and convection effectively mobilizes oil in large pore bodies.Developed and homogeneous pore structures enhance CO_(2)displacement efficiency,whereas CO_(2)flows along the main flow channels in heterogeneous pore structures,resulting in lower displacement efficiency.Diffusion plays a crucial role in CO_(2)storage within porous media.At low injection rates,dissolved CO_(2)is trapped in poorly connected and blind-end pores.The injection rate is negatively correlated with the sequestration factor.
基金National Natural Science Foundation of China,Grant/Award Number:12274118Double First Class University Plan,Grant/Award Number:C176220100042+2 种基金National Natural Science Foundation of China-Yunnan Joint Fund,Grant/Award Number:U2002213Open Foundation of Guangxi Key Laboratory of Processing for Non-Ferrous Metals and Featured Materials,Grant/Award Number:2022GXYSOF10Henan Center for Outstanding Overseas Scientists,Grant/Award Number:GZS2023007.
文摘Zn-CO_(2)batteries(ZCBs)are promising for CO_(2)conversion and electric energy release.However,the ZCBs couple the electrochemical CO_(2)reduction(ECO_(2)R)with the oxygen evolution reaction and competitive hydrogen evolution reaction,which normally causes ultrahigh charge voltage and CO_(2)conversion efficiency attenuation,thereby resulting in~90%total power consumption.Herein,isolated FeN_(3)sites encapsulated in hierarchical porous carbon nanoboxes(Fe-HPCN,derived from the thermal activation process of ferrocene and polydopamine-coated cubic ZIF-8)were proposed for hydrazine-assisted rechargeable ZCBs based on ECO_(2)R(discharging process:CO_(2)+2H+→CO+H_(2)O)and hydrazine oxidation reaction(HzOR,charging process:N_(2)H_(4)+4OH−→N_(2)+4H_(2)O+4e^(−)).The isolated FeN_(3)endows the HzOR with a lower overpotential and boosts the ECO_(2)R with a 96%CO Faraday efficiency(FECO).Benefitting from the bifunctional ECO_(2)R and HzOR catalytic activities,the homemade hydrazine-assisted rechargeable ZCBs assembled with the Fe-HPCN air cathode exhibited an ultralow charge voltage(decreasing by~1.84 V),excellent CO selectivity(FECO close to 100%),and high 89%energy efficiency.In situ infrared spectroscopy confirmed that Fe-HPCN can generate rate-determining*N_(2)and*CO intermediates during HzOR and ECO_(2)R.This paper proposes FeN_(3)centers for bifunctional ECO_(2)R/HzOR performance and further presents the pioneering achievements of ECO_(2)R and HzOR for hydrazine-assisted rechargeable ZCBs.
文摘MXene is an emerging class of two-dimensional(2D)layered transition metal carbides or nitrides.Due to the highly tunable components and surface functional groups,it holds great potential in electrocatalytic hydrogen evolution reaction(HER).However,MXene nanosheet suffers from a strong tendency to restack and a lack of active edge sites.In this work,the porous Ti_(3)C_(2)T_(x)was synthesized by an oxidation and etching two-step strategy and then characterized by a series of spectroscopic techniques.The obtained porous Ti_(3)C_(2)T_(x)possesses a large number of in-plane pores.This not only creates abundant active edge sites but also enhances the mass transfer and increases the accessibility of the active sites.Compared with Ti_(3)C_(2)T_(x),in a 0.5 mol/L H_(2)SO_(4)electrolyte,the porous Ti_(3)C_(2)T_(x)shows a 65.6%higher electrochemical surface area(ECSA)(440 mF/cm^(2)),a 95.2%lower charge transfer resistance(12.8Ω),and a 69.8%lower Tafel slope(144 mV/dec),and thus exhibits lower overpotential with good stability at a current density of 10 mA/cm^(2).At the same time,the HER performance of the porous Ti_(3)C_(2)T_(x)can be further enhanced by near-infrared laser irradiation based on the localized surface plasmon resonance effect.
文摘Chemical vapor deposition is the predominant method to prepare MgAl_(2)O_(4)fibers.However,it faces several challenges,including exorbitantly high reaction temperatures,substantial production costs,and relatively low yields.In this study,porous MgAl_(2)O_(4)fibers were fabricated through a solid-state reaction method,utilizing MgSO_(4)·5Mg(OH)_(2)·3H_(2)O whiskers as templates,mixed with either aluminum sol orα-Al_(2)O_(3)micropowder.The impact of various parameters on the synthesis of porous MgAl_(2)O_(4)fibres was systematically investigated,including the heat treatment temperature(1000,1100 and 1300℃),the holding time(3 and 10 h)and the aluminum source(aluminum sol orα-Al_(2)O_(3)micropowder).The results reveal that:(1)in comparison with fibers synthesized usingα-Al_(2)O_(3)as the aluminum source,those prepared with aluminum sol exhibit a significantly higher generation amount of MgAl_(2)O_(4);(2)as the heat treatment temperature increases,Al_(2)O_(3)gradually reacts with MgO,continuously increasing the formation amount of porous MgAl_(2)O_(4)with small and uniformly distributed nanopores,and the synthesized porous MgAl_(2)O_(4)fibres have small and uniform nanopores;(3)the optimal synthesis process involves using aluminum sol as the aluminum source and firing at 1300℃ for 3 h.
基金supported by the National Key R&D Program of China(2022YFB3803700)National Natural Science Foundation of China(52171186)+1 种基金Young Elite Scientists Sponsorship Program by CAST(2023QNRC001)support from“Zhiyuan Honor Program”for doctoral students,Shanghai Jiao Tong University.
文摘Nanoconfinement is a promising approach to simultaneously enhance the thermodynamics,kinetics,and cycling stability of hydrogen storage materials.The introduction of supporting scaffolds usually causes a reduction in the total hydrogen storage capacity due to“dead weight.”Here,we synthesize an optimized N-doped porous carbon(rN-pC)without heavy metal as supporting scaffold to confine Mg/MgH_(2) nanoparticles(Mg/MgH_(2)@rN-pC).rN-pC with 60 wt%loading capacity of Mg(denoted as 60 Mg@rN-pC)can adsorb and desorb 0.62 wt%H_(2) on the rN-pC scaffold.The nanoconfined MgH_(2) can be chemically dehydrided at 175℃,providing~3.59 wt%H_(2) with fast kinetics(fully dehydrogenated at 300℃ within 15 min).This study presents the first realization of nanoconfined Mg-based system with adsorption-active scaffolds.Besides,the nanoconfined MgH_(2) formation enthalpy is reduced to~68 kJ mol^(−1) H_(2) from~75 kJ mol^(−1) H_(2) for pure MgH_(2).The composite can be also compressed to nanostructured pellets,with volumetric H_(2) density reaching 33.4 g L^(−1) after 500 MPa compression pressure,which surpasses the 24 g L^(−1) volumetric capacity of 350 bar compressed H_(2).Our approach can be implemented to the design of hybrid H_(2) storage materials with enhanced capacity and desorption rate.
基金Project(1254G024)supported by the Young Core Instructor Foundation from Heilongjiang Educational Committee,ChinaProject(2012RFQXS113)supported by Scientific and Technological Innovation Talents of Harbin,China
文摘Both Ti foil and porous Ti were anodized in 0.5%HF and in ethylene glycol electrolyte containing 0.5%NH4F(mass fraction) separately. The results show that TiO2 nanotubes can be formed on Ti foil by both processes, whereas TiO2 nanotubes can be formed on porous Ti only in the second process. The overhigh current density led to the failure of the formation nanotubes on porous Ti in 0.5%HF electrolyte. TiO2 nanotubes were characterized by SEM and XRD. TiO2 nanotubes on porous Ti were thinner than those on Ti foil. Anatase was formed when TiO2 nanotubes were annealed at 400 °C and fully turned into rutile at 700 °C. To obtain good photodegradation, the optimal heat treatment temperature of TiO2 nanotubes was 450 °C. The porosity of the substrates influenced photodegradation properties. TiO2 nanotubes on porous Ti with 60% porosity had the best photodegradation.
基金supported by the National Science Foundation for Young Scientists of China (51202171)~~
文摘A molten salt method was developed to prepare porous La1‐xSrxMn0.8Fe0.2O3 （0≤ x ≤ 0.6） micro‐spheres using hierarchical porous δ‐MnO2 microspheres as a template in eutectic NaNO3‐KNO3. X‐ray diffraction patterns showed that single phase LaMn0.8Fe0.2O3 with good crystallinity was syn‐thesized at 450℃ after 4 h. Transmission electron microscope images exhibited that the LaMn0.8Fe0.2O3 sample obtained at 450？？ after 4 h possessed a porous spherical morphology com‐posed of aggregated nanocrystallites. Field emission scanning electron microscope images indicated that the growth of the porous LaMn0.8Fe0.2O3 microspheres has two stages. SEM pictures showed that a higher calcination temperature than 450？？ had an adverse effect on the formation of a po‐rous spherical structure. The LaMn0.8Fe0.2O3 sample obtained at 450？？ after 4 h displayed a high BET surface area of 55.73 m2/g with a pore size of 9.38 nm. Fourier transform infrared spectra suggested that Sr2＋ions entered the A sites and induced a decrease of the binding energy between Mn and O. The CO conversion with the La1‐xSrxMn0.8Fe0.2O3 （0≤x≤0.6） samples indicated that the La0.4Sr0.6Mn0.8Fe0.2O3 sample had the best catalytic activity and stability. Further analysis by X‐ray photoelectron spectroscopy demonstrated that Sr2＋doping altered the content of Mn4＋ions, oxygen vacancies and adsorbed oxygen species on the surface, which affected the catalytic performance for CO oxidation.
文摘The solution of H 2O 2 is proposed to post-treat thick porous silicon (PS) films.The prepared PS film as the cathode is applied about 10mA/cm 2 current in mixture of ethanol,HF,and H 2O 2 solutions,which is expected to improve the stability and the smoothness of the surface and the mechanical property of the thick porous silicon films.The microstructure of the PS thick films with thicknesse of 20μm and 70μm has been studied.The SEM images show significant improved smoothness on surface of PS films,and XRD spectra suggest the formation of oxide layer after post-treating in H 2O 2.
