The scarcity of wettability,insufficient active sites,and low surface area of graphite felt(GF)have long been suppressing the performance of vanadium redox flow batteries(VRFBs).Herein,an ultra-homogeneous multipledim...The scarcity of wettability,insufficient active sites,and low surface area of graphite felt(GF)have long been suppressing the performance of vanadium redox flow batteries(VRFBs).Herein,an ultra-homogeneous multipledimensioned defect,including nano-scale etching and atomic-scale N,O codoping,was used to modify GF by the molten salt system.NH_(4)Cl and KClO_(3) were added simultaneously to the system to obtain porous N/O co-doped electrode(GF/ON),where KClO_(3) was used to ultra-homogeneously etch,and O-functionalize electrode,and NH4Cl was used as N dopant,respectively.GF/ON presents better electrochemical catalysis for VO_(2)+/VO_(2)+ and V3+/V2+ reactions than only O-functionalized electrodes(GF/O)and GF.The enhanced electrochemical properties are attributed to an increase in active sites,surface area,and wettability,as well as the synergistic effect of N and O,which is also supported by the density functional theory calculations.Further,the cell using GF/ON shows higher discharge capacity,energy efficiency,and stability for cycling performance than the pristine cell at 140 mA cm^(−2) for 200 cycles.Moreover,the energy efficiency of the modified cell is increased by 9.7% from 55.2% for the pristine cell at 260 mA cm^(−2).Such an ultra-homogeneous etching with N and O co-doping through“boiling”molten salt medium provides an effective and practical application potential way to prepare superior electrodes for VRFB.展开更多
Hydrogen peroxide synthesis by electro-reduction of O_(2) to substitute the current anthraquinone process has attracted a great deal of attention. Low oxygen utilization rate and low hydrogen peroxide production remai...Hydrogen peroxide synthesis by electro-reduction of O_(2) to substitute the current anthraquinone process has attracted a great deal of attention. Low oxygen utilization rate and low hydrogen peroxide production remain obstacles to electro-Fenton application. In situ H_(2)O_(2) generated by electrochemical reaction depends on the electrochemical performance of the cathode and the structure of the reactor. Here, novel graphite felt(GF) modified by La-doped CeO_(2)(La-CeO_(2)) was developed as a cathode. A new double chamber electro-Fenton reactor was proposed, where an organic ultrafiltration membrane was used to prevent H_(2)O_(2) from spreading to the anode. The effects of hydrothermal temperature, time and urea concentration on the electrochemical properties of graphite felt were investigated. The accumulated concentration of H_(2)O_(2) on the modified cathode reached 218.4 mg·L^(-1)in 1 h when the optimal conditions of hydrothermal temperature 120 ℃ and urea concentration 0.55%(mass) in 24 h. The degradation rate of methyl orange reached 98.29%. The new electro-Fenton reactor can efficiently produce hydrogen peroxide to degrade various organic substances and has a high potential for treating wastewater in the chemical industry.展开更多
The graphite felt was oxidized at a positive electrode potential in sulfuric acid solution.The electrochemical performance of the treated graphite felt served as electrode for vanadium redox battery was investigated w...The graphite felt was oxidized at a positive electrode potential in sulfuric acid solution.The electrochemical performance of the treated graphite felt served as electrode for vanadium redox battery was investigated with FT-IR,SEM,XPS,BET,cyclic voltammetry and testing VRB system,respectively.The results show that the molar ratio of O to C increases from 0.085 to 0.15 due to the increase of—COOH functional groups during electrochemical oxidation treatment,and the GF surface is eroded by electrochemical oxidation,resulting in the surface area increase from 0.33 m2/g to 0.49 m 2/g.The VRB with modified GF electrode exhibits excellent performance under a current density of 30 mA/cm 2 .The average current efficiency reaches 94%and average voltage efficiency reaches 85%.The improvement of electrochemical activity for the electrode is ascribed to the increase of the number of—COOH group and the special surface of GF.展开更多
The cerium-based redox flow battery(RFB)is regarded as a compelling gridscale energy storage technology to revolutionize the utilization of renewable energy by storing the energy in liquid electrolytes.However,its wid...The cerium-based redox flow battery(RFB)is regarded as a compelling gridscale energy storage technology to revolutionize the utilization of renewable energy by storing the energy in liquid electrolytes.However,its widespread implementation is impeded by the cerium redox reactions that exhibit slow kinetics on commercial graphite felt(GF)electrodes.Surface functionalization may be an available activation strategy to achieve a significant boost in the electrochemical performance of GFs.However,conventional chemical and/or electrochemical routes for the surface functionalization of GFs suffer from the issues of complication,and the deterioration of the resulting modified electrode surface over long-term cycle processes leads to catalytic activity decline.Here,we develop a facile and general strategy for introducing the functional groups to the electrode through the addition of L-cysteine into electrolytes.The-COOH,-NH_(2),and-SH groups in L-cysteine can induce oxygen/nitrogen/sulfur trifunctional doping on GF surfaces with lower deterioration rates,which enables the activated GFs to demonstrate a promising electrocatalytic activity toward cerium redox reactions and excellent durability when used as a cerium-based RFB electrode.This study proposes a rational strategy to overcome the intrinsic limitations of existing modification techniques for GFs and provides a potential pathway toward high-performance RFBs.展开更多
PAN-based graphite felt （PGF） treated in 98% sulphuric acid for 5 h and then kept at 450 ℃ for 2 h was evaluated for their electrochemical performance as electrodes of vanadium redox battery （VRB）. Structure and ...PAN-based graphite felt （PGF） treated in 98% sulphuric acid for 5 h and then kept at 450 ℃ for 2 h was evaluated for their electrochemical performance as electrodes of vanadium redox battery （VRB）. Structure and characteristic of treated PAN-based graphite felt （TPGF） were determined by means of Fourier Transform Infi-ared Spectroscopy, Scanning Electron Microscopy, Brunauer-Emmett-Teller surface area analysis and VRB test system. The results show that the acid and heat synergistic effect increase the number of --COOH functional groups on the PGF surface, and the PGF is eroded by sulphuric acid oxidation, resulting in the surface area increases from 0.31 m^2/g to 0.45 m^2/g. The V（ Ⅱ ）/V（Ⅲ） redox reaction is electrochemically reversible on the TPGF electrode, while the V（Ⅳ）/V（Ⅴ） couple is a quasi reversible process. The diffusion coefficients of the oxidation for V（Ⅳ）/V（Ⅴ） obtained from the scope of peak current Ip vs scan rate v^1/2 is 4.4×10^-5 cm^2/s. The improvement of electrochemical activity for the electrode is mainly ascribed to the increase of the number of ---COOH groups on the TPGF, which behaves as active sites catalyzing the vanadium species reactions and accelerating electron transfer reaction and oxygen transfer.展开更多
铁铬氧化还原液流电池(ICRFB)是一种具有成本效益的可规模化储能系统,其利用资源丰富、低成本的铬和铁作为电解液的活性物质。然而,ICRFB存在Cr^(3+)/Cr^(2+)电化学活性低、负极易产生严重的析氢反应(HER)等问题。本文报道了一种简单的...铁铬氧化还原液流电池(ICRFB)是一种具有成本效益的可规模化储能系统,其利用资源丰富、低成本的铬和铁作为电解液的活性物质。然而,ICRFB存在Cr^(3+)/Cr^(2+)电化学活性低、负极易产生严重的析氢反应(HER)等问题。本文报道了一种简单的合成策略,即通过自聚合和湿化学还原方法结合煅烧处理,在氮掺杂石墨毡(GF)表面沉积了非晶态铋(Bi)纳米颗粒(NPs),其作为ICRFB的负极材料时可展示出高效的电化学性能。生成的BiNPs与H+形成中间体,极大地抑制了HER副反应。此外,Bi的引入和GF表面的N掺杂通过协同作用显著提高了Fe^(2+)/Fe^(3+)和Cr^(3+)/Cr^(2+)的电化学活性,降低了电荷传递电阻,提高了反应传质速率。在不同的电流密度下,经25次循环,库仑效率仍高达97.7%。在60.0 mA cm^(-2)电流密度下,能量效率达到85.8%,超过了许多其他报道的材料。循环100次后容量达到862.7 mAh/L,约为GF的5.3倍。展开更多
Developing non-noble-metal oxygen evolution reaction(OER) electrocatalysts with high performance is critical to electrocatalytic water splitting. In this work, we fabricated Co Fe-layered double hydroxide(LDH) nanowir...Developing non-noble-metal oxygen evolution reaction(OER) electrocatalysts with high performance is critical to electrocatalytic water splitting. In this work, we fabricated Co Fe-layered double hydroxide(LDH) nanowire arrays on graphite felt(Co Fe-LDH/GF) via a hydrothermal method. The Co Fe-LDH/GF, as a robust integrated 3 D OER anode, exhibits excellent catalytic activity with the need of low overpotential of 252 and 285 mV to drive current densities of 10 and 100 mA/cm^(2) in 1.0 mol/L KOH, respectively. In addition, it also maintains electrochemical durability for at least 24 h. This work would open up avenues for the development of GF like attractive catalyst supports for oxygen evolution applications.展开更多
A mild and simple synthesis process for large-scale vanadium redox flow batteries(VRFBs)energy storage systems is desirable.A graphite felt/Mn O_2(GF-MNO)composite electrode with excellent electrocatalytic activity to...A mild and simple synthesis process for large-scale vanadium redox flow batteries(VRFBs)energy storage systems is desirable.A graphite felt/Mn O_2(GF-MNO)composite electrode with excellent electrocatalytic activity towards VO^(2+)/VO_2^+redox couples in a VRFB was synthesized by a one-step hydrothermal process.The resulting GF-MNO electrodes possess improved electrochemical kinetic reversibility of the vanadium redox reactions compared to pristine GF electrodes,and the corresponding energy efficiency and discharge capacity at 150 m A cm^(-2)are increased by 12.5%and 40%,respectively.The discharge capacity is maintained at 4.8 A h L^(-1)at the ultrahigh current density of 250 m A cm^(-2).Above all,80%of the energy efficiency of the GF-MNO composite electrodes is retained after 120 charge-discharge cycles at 150 m A cm^(-2).Furthermore,these electrodes demonstrated that more evenly distributed catalytic active sites were obtained from the Mn O_2particles under acidic conditions.The proposed synthetic route is facile,and the raw materials are low cost and environmentally friendly.Therefore,these novel GF-MNO electrodes hold great promise in large-scale vanadium redox flow battery energy storage systems.展开更多
E-peroxone(EP)was one of the most attractive AOPs for removing refractory organic compounds from water,but the high energy consumption for in situ generating H_(2)O_(2) and its low reaction efficiency for activating O...E-peroxone(EP)was one of the most attractive AOPs for removing refractory organic compounds from water,but the high energy consumption for in situ generating H_(2)O_(2) and its low reaction efficiency for activating O_(3) under acidic conditions made the obstacles for its practical application.In this study,cerium oxide was loaded on the surface of graphite felt(GF)by the hydrothermal method to construct the efficient electrode(CeO_(x)/GF)for mineralizing carbamazepine(CBZ)via EP process.CeO_(x)/GF was an efficient cathode,which led to 69.4%TOC removal in CeO_(x)/GF-EP process with current intensity of 10 mA in 60 min.Moreover,CeO_(x)/GF had the flexible application in the pH range from 5.0 to 9.0,TOC removal had no obvious decline with decrease of pH.Comparative characterizations showed that CeO_(x)could enhance surface hydrophilicity and reduce the charge-transfer resistance of GF.About 5.4 mg/L H_(2)O_(2) generated in CeO_(x)/GF-EP process,which was 2.1 times as that in GF-EP process.The greater ozone utility was also found in CeO_(x)/GF-EP process.More O_(3) was activated into hydroxyl radicals,which accounted for the mineralization of CBZ.An interfacial electron transfer process was revealed,which involved the function of oxygen vacancies and Ce^(3+)/Ce^(4+)redox cycle.CeO_(x)/GF had the good recycling property in fifth times'use.展开更多
In this study,aqueous organic redox flow batteries(AORFBs)with NaCl as supporting electrolyte were investigated.In AORFBs,the chlorine evolution reaction should be retarded,not the hydrogen evolution reaction.To enhan...In this study,aqueous organic redox flow batteries(AORFBs)with NaCl as supporting electrolyte were investigated.In AORFBs,the chlorine evolution reaction should be retarded,not the hydrogen evolution reaction.To enhance the catalytic activity of the graphite fel(GF)electrode,the metal oxides were proposed to decorate on the GF surface.Among the loading oxides,significant enhancement of the mass transfer and reaction activity was obtained by the presence of LaSrOx nanoparticles.X-Ray photoclectron spectroscopy and contact angle measurements revealed that the content of oxygen-containing groups and the hydrophilicity were remarkably inereased.After the electrode assem-bled in the battery,the LaSrO/GF electrode presented huge enhancement of the battery performance,obviously increasing in the battery capacity and efficiency.At a current of 50 Am/cm^(2),the energy efficiency(EE)of the battery increased from 54.76%to 61.37%by the LaSrO/GF electrode.Furthermore,the cyclability of the system tested that no obviously fading was observed after 100 cycles,signifying the excellent stability of the LaSrOx/GF electrode.展开更多
基金supported by the National Natural Science Foundation of China(No.51872090)Natural Science Foundation of Hebei Province(No.E2019209433,E2022209158)Colleges and Universities in Hebei Province Science and Technology Research Project(No.JZX2024026).
文摘The scarcity of wettability,insufficient active sites,and low surface area of graphite felt(GF)have long been suppressing the performance of vanadium redox flow batteries(VRFBs).Herein,an ultra-homogeneous multipledimensioned defect,including nano-scale etching and atomic-scale N,O codoping,was used to modify GF by the molten salt system.NH_(4)Cl and KClO_(3) were added simultaneously to the system to obtain porous N/O co-doped electrode(GF/ON),where KClO_(3) was used to ultra-homogeneously etch,and O-functionalize electrode,and NH4Cl was used as N dopant,respectively.GF/ON presents better electrochemical catalysis for VO_(2)+/VO_(2)+ and V3+/V2+ reactions than only O-functionalized electrodes(GF/O)and GF.The enhanced electrochemical properties are attributed to an increase in active sites,surface area,and wettability,as well as the synergistic effect of N and O,which is also supported by the density functional theory calculations.Further,the cell using GF/ON shows higher discharge capacity,energy efficiency,and stability for cycling performance than the pristine cell at 140 mA cm^(−2) for 200 cycles.Moreover,the energy efficiency of the modified cell is increased by 9.7% from 55.2% for the pristine cell at 260 mA cm^(−2).Such an ultra-homogeneous etching with N and O co-doping through“boiling”molten salt medium provides an effective and practical application potential way to prepare superior electrodes for VRFB.
基金supported by the Tianjin Synthetic Biotechnology Innovation Capacity Improvement Project (TSBICIP-KJGG003)Qinglan Plan of the Jiangsu Education Department。
文摘Hydrogen peroxide synthesis by electro-reduction of O_(2) to substitute the current anthraquinone process has attracted a great deal of attention. Low oxygen utilization rate and low hydrogen peroxide production remain obstacles to electro-Fenton application. In situ H_(2)O_(2) generated by electrochemical reaction depends on the electrochemical performance of the cathode and the structure of the reactor. Here, novel graphite felt(GF) modified by La-doped CeO_(2)(La-CeO_(2)) was developed as a cathode. A new double chamber electro-Fenton reactor was proposed, where an organic ultrafiltration membrane was used to prevent H_(2)O_(2) from spreading to the anode. The effects of hydrothermal temperature, time and urea concentration on the electrochemical properties of graphite felt were investigated. The accumulated concentration of H_(2)O_(2) on the modified cathode reached 218.4 mg·L^(-1)in 1 h when the optimal conditions of hydrothermal temperature 120 ℃ and urea concentration 0.55%(mass) in 24 h. The degradation rate of methyl orange reached 98.29%. The new electro-Fenton reactor can efficiently produce hydrogen peroxide to degrade various organic substances and has a high potential for treating wastewater in the chemical industry.
基金Project(02-09-01)supported by Pangang Group Pangzhihua Iron and Steel Research Institute,China
文摘The graphite felt was oxidized at a positive electrode potential in sulfuric acid solution.The electrochemical performance of the treated graphite felt served as electrode for vanadium redox battery was investigated with FT-IR,SEM,XPS,BET,cyclic voltammetry and testing VRB system,respectively.The results show that the molar ratio of O to C increases from 0.085 to 0.15 due to the increase of—COOH functional groups during electrochemical oxidation treatment,and the GF surface is eroded by electrochemical oxidation,resulting in the surface area increase from 0.33 m2/g to 0.49 m 2/g.The VRB with modified GF electrode exhibits excellent performance under a current density of 30 mA/cm 2 .The average current efficiency reaches 94%and average voltage efficiency reaches 85%.The improvement of electrochemical activity for the electrode is ascribed to the increase of the number of—COOH group and the special surface of GF.
基金Natural Science Foundation of Liaoning Province,Grant/Award Number:2020-MZLH-40High-Level Talent Innovation Support Program of Dalian City,Grant/Award Number:2019RQ076National Natural Science Foundation of China,Grant/Award Numbers:21801034,51732007,51872033。
文摘The cerium-based redox flow battery(RFB)is regarded as a compelling gridscale energy storage technology to revolutionize the utilization of renewable energy by storing the energy in liquid electrolytes.However,its widespread implementation is impeded by the cerium redox reactions that exhibit slow kinetics on commercial graphite felt(GF)electrodes.Surface functionalization may be an available activation strategy to achieve a significant boost in the electrochemical performance of GFs.However,conventional chemical and/or electrochemical routes for the surface functionalization of GFs suffer from the issues of complication,and the deterioration of the resulting modified electrode surface over long-term cycle processes leads to catalytic activity decline.Here,we develop a facile and general strategy for introducing the functional groups to the electrode through the addition of L-cysteine into electrolytes.The-COOH,-NH_(2),and-SH groups in L-cysteine can induce oxygen/nitrogen/sulfur trifunctional doping on GF surfaces with lower deterioration rates,which enables the activated GFs to demonstrate a promising electrocatalytic activity toward cerium redox reactions and excellent durability when used as a cerium-based RFB electrode.This study proposes a rational strategy to overcome the intrinsic limitations of existing modification techniques for GFs and provides a potential pathway toward high-performance RFBs.
基金Project (03GKY3015) supported by the Foundation of Hunan Provincial Department of Science and Technology
文摘PAN-based graphite felt （PGF） treated in 98% sulphuric acid for 5 h and then kept at 450 ℃ for 2 h was evaluated for their electrochemical performance as electrodes of vanadium redox battery （VRB）. Structure and characteristic of treated PAN-based graphite felt （TPGF） were determined by means of Fourier Transform Infi-ared Spectroscopy, Scanning Electron Microscopy, Brunauer-Emmett-Teller surface area analysis and VRB test system. The results show that the acid and heat synergistic effect increase the number of --COOH functional groups on the PGF surface, and the PGF is eroded by sulphuric acid oxidation, resulting in the surface area increases from 0.31 m^2/g to 0.45 m^2/g. The V（ Ⅱ ）/V（Ⅲ） redox reaction is electrochemically reversible on the TPGF electrode, while the V（Ⅳ）/V（Ⅴ） couple is a quasi reversible process. The diffusion coefficients of the oxidation for V（Ⅳ）/V（Ⅴ） obtained from the scope of peak current Ip vs scan rate v^1/2 is 4.4×10^-5 cm^2/s. The improvement of electrochemical activity for the electrode is mainly ascribed to the increase of the number of ---COOH groups on the TPGF, which behaves as active sites catalyzing the vanadium species reactions and accelerating electron transfer reaction and oxygen transfer.
文摘铁铬氧化还原液流电池(ICRFB)是一种具有成本效益的可规模化储能系统,其利用资源丰富、低成本的铬和铁作为电解液的活性物质。然而,ICRFB存在Cr^(3+)/Cr^(2+)电化学活性低、负极易产生严重的析氢反应(HER)等问题。本文报道了一种简单的合成策略,即通过自聚合和湿化学还原方法结合煅烧处理,在氮掺杂石墨毡(GF)表面沉积了非晶态铋(Bi)纳米颗粒(NPs),其作为ICRFB的负极材料时可展示出高效的电化学性能。生成的BiNPs与H+形成中间体,极大地抑制了HER副反应。此外,Bi的引入和GF表面的N掺杂通过协同作用显著提高了Fe^(2+)/Fe^(3+)和Cr^(3+)/Cr^(2+)的电化学活性,降低了电荷传递电阻,提高了反应传质速率。在不同的电流密度下,经25次循环,库仑效率仍高达97.7%。在60.0 mA cm^(-2)电流密度下,能量效率达到85.8%,超过了许多其他报道的材料。循环100次后容量达到862.7 mAh/L,约为GF的5.3倍。
基金supported by the National Natural Science Foundation of China (No.22072015)。
文摘Developing non-noble-metal oxygen evolution reaction(OER) electrocatalysts with high performance is critical to electrocatalytic water splitting. In this work, we fabricated Co Fe-layered double hydroxide(LDH) nanowire arrays on graphite felt(Co Fe-LDH/GF) via a hydrothermal method. The Co Fe-LDH/GF, as a robust integrated 3 D OER anode, exhibits excellent catalytic activity with the need of low overpotential of 252 and 285 mV to drive current densities of 10 and 100 mA/cm^(2) in 1.0 mol/L KOH, respectively. In addition, it also maintains electrochemical durability for at least 24 h. This work would open up avenues for the development of GF like attractive catalyst supports for oxygen evolution applications.
基金supported by the Ministry of Science and Technology of China (2016YFA0202500)the National Natural Science Foundation of China (51772093)the National key Research and Development Program of China (2017YFD0301507)
文摘A mild and simple synthesis process for large-scale vanadium redox flow batteries(VRFBs)energy storage systems is desirable.A graphite felt/Mn O_2(GF-MNO)composite electrode with excellent electrocatalytic activity towards VO^(2+)/VO_2^+redox couples in a VRFB was synthesized by a one-step hydrothermal process.The resulting GF-MNO electrodes possess improved electrochemical kinetic reversibility of the vanadium redox reactions compared to pristine GF electrodes,and the corresponding energy efficiency and discharge capacity at 150 m A cm^(-2)are increased by 12.5%and 40%,respectively.The discharge capacity is maintained at 4.8 A h L^(-1)at the ultrahigh current density of 250 m A cm^(-2).Above all,80%of the energy efficiency of the GF-MNO composite electrodes is retained after 120 charge-discharge cycles at 150 m A cm^(-2).Furthermore,these electrodes demonstrated that more evenly distributed catalytic active sites were obtained from the Mn O_2particles under acidic conditions.The proposed synthetic route is facile,and the raw materials are low cost and environmentally friendly.Therefore,these novel GF-MNO electrodes hold great promise in large-scale vanadium redox flow battery energy storage systems.
基金funded by the National Natural Science Foundation(No.51978288)Natural Science Foundation of Guangdong Province(No.2019A1515012202)Major Science and Technology Program for Water Pollution Control and Treatment in China(No.2017ZX07202-004).
文摘E-peroxone(EP)was one of the most attractive AOPs for removing refractory organic compounds from water,but the high energy consumption for in situ generating H_(2)O_(2) and its low reaction efficiency for activating O_(3) under acidic conditions made the obstacles for its practical application.In this study,cerium oxide was loaded on the surface of graphite felt(GF)by the hydrothermal method to construct the efficient electrode(CeO_(x)/GF)for mineralizing carbamazepine(CBZ)via EP process.CeO_(x)/GF was an efficient cathode,which led to 69.4%TOC removal in CeO_(x)/GF-EP process with current intensity of 10 mA in 60 min.Moreover,CeO_(x)/GF had the flexible application in the pH range from 5.0 to 9.0,TOC removal had no obvious decline with decrease of pH.Comparative characterizations showed that CeO_(x)could enhance surface hydrophilicity and reduce the charge-transfer resistance of GF.About 5.4 mg/L H_(2)O_(2) generated in CeO_(x)/GF-EP process,which was 2.1 times as that in GF-EP process.The greater ozone utility was also found in CeO_(x)/GF-EP process.More O_(3) was activated into hydroxyl radicals,which accounted for the mineralization of CBZ.An interfacial electron transfer process was revealed,which involved the function of oxygen vacancies and Ce^(3+)/Ce^(4+)redox cycle.CeO_(x)/GF had the good recycling property in fifth times'use.
基金Supported by the Natural Science Foundation of Jiangsu Province,China(No.BK20160297).
文摘In this study,aqueous organic redox flow batteries(AORFBs)with NaCl as supporting electrolyte were investigated.In AORFBs,the chlorine evolution reaction should be retarded,not the hydrogen evolution reaction.To enhance the catalytic activity of the graphite fel(GF)electrode,the metal oxides were proposed to decorate on the GF surface.Among the loading oxides,significant enhancement of the mass transfer and reaction activity was obtained by the presence of LaSrOx nanoparticles.X-Ray photoclectron spectroscopy and contact angle measurements revealed that the content of oxygen-containing groups and the hydrophilicity were remarkably inereased.After the electrode assem-bled in the battery,the LaSrO/GF electrode presented huge enhancement of the battery performance,obviously increasing in the battery capacity and efficiency.At a current of 50 Am/cm^(2),the energy efficiency(EE)of the battery increased from 54.76%to 61.37%by the LaSrO/GF electrode.Furthermore,the cyclability of the system tested that no obviously fading was observed after 100 cycles,signifying the excellent stability of the LaSrOx/GF electrode.
