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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2022 ·Vol. 46 ·期 14 ·19357-19367 · IF 4.672

A novel Nafion-Functionalized Polyethersulfone(PES)-based ion-permselective separator for high performance Li-O2 batteries using LiI as a redox mediator

Jiuqing Liu,Feifei Song,Junying He,Zikun Hong,Qihou Li,Ya Chen,Lishun Bai,Fanli Zeng,Chen Cheng,Zehao Chen

Summary Owing to its unparalleled theoretical energy density, the Li-O 2 batteries are thought to be one of the most promising energy storage systems, but its application is seriously hindered by its potential safety risks arising from the passivation and corrosion of lithium anode. To address these issues, it is an efficient way to develop functionalized separator that could prevent the migration of anions and macromolecules from cathode toward anode. Herein, a novel Nafion-functionalized polyethersulfone (PES)-based ion-permselective separator was prepared by using non-solvent induced phase separation (NIPS) method. The Nafion ensures a better physical strength of the composite separator, and further characterizations show that the obtained composite separator owns good ionic conductivity (0.52 mS cm −1 ), high lithium ion migration number (0.80), and better cyclic stability (120 cycles, 1000 mAh g −1 ). Consequently, the composite separator serves as an excellent candidate to solve the “shuttle effect” of redox mediators (RMs), the assembled Li-O 2 battery with composite separator adding LiI as RMs presents lower charge overpotential and longer cycle stability (170 cycles, 1000 mAh g −1 ).

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2020 ·Vol. 44 ·期 5 ·3626-3639 · IF 3.741

Preparation and characterization of urea/ammonia bromide composite phase change material

Biao Liu,Xuelai Zhang,Jun Ji,Weisan Hua,Fa Mao

Summary In order to find phase change materials that can be better applied in the field of solar collectors, the phase change heat storage properties of urea (U) and ammonium bromide (AB) were studied. The eutectic ratio of UAB was found by the Edison method, and different additives were added to UAB by dipping and mixing. The structure and property of the composites were characterized by X-ray powder diffraction (XRD), scanning electron microscope (SEM), differential scanning calorimetry (DSC), and TG/TGA, respectively. The results showed that the eutectic ratio of UAB was 6:3; it was weakly acidic after melting not layered. When 6-wt% EG and 1-wt% nanometer titanium dioxide (TiO 2 ) were added, the thermal conductivity of the material increased by 3.62 times; the thermal diffusivity was increased by 6.77 times. When the mass fraction of EG is between 1% and 6%, the larger the mass fraction of EG, the greater the thermal conductivity of the material. After 1000 cycles, the composite material performance was stable; at the same time, the used materials can be used as fertilizers to solve the problem of material pollution, which indicated that the prepared UAB/TiO2/EG composite PCMs had great application prospect in the field of solar collectors.

研究领域: 材料科学 · 能源工程
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2021 ·Vol. 45 ·期 6 ·8724-8734 · IF 5.164

Effect of improved trialkyl phosphine oxides waste content on phase composition and density of spark plasma sintered Gd2Zr2O7 ceramics

Ningning He,Guilin Wei,Pan Wen,Wenhong Han,Chen Xu,Xiaoyan Shu,Fen Luo,Shunzhang Chen,Lan Wang,Yi Xie,Xirui Lu

Summary As a rapid sintering method, spark plasma sintering (SPS) process has been widely applied to immobilize nuclear waste. In this work, trialkyl phosphine oxides (TRPO) were immobilized by the mixture of Gd 2 O 3 and ZrO 2 with SPS proceedings at 1650°C in 3 minutes. X-ray diffraction results present that the solid solubility is 10 to 20 wt% and all the sintered samples show a fluorite structure. Raman spectroscopy results show that the order degree of structure decreases as waste content increases. The lattice parameters decrease with the increasing doped waste content indicating the success of waste immobilization. Densities decrease for the sample with higher waste content which mainly caused by the existence of pores. Scanning electron microscope-energy dispersive X-ray spectroscopy and backscattered electron results perform the microstructure of the sintered sample. Furthermore, the leaching test shows that the sample has a considerable chemical stability. This study confirmed the possibility of rapid consolidation of Gd 2 Zr 2 O 7 bulk, dense ceramic with up to 10 ~ 20 wt% of immobilized TRPO waste. Highlights Multi-nuclides waste was rapidly immobilized by Gd 2 Zr 2 O 7 via SPS process. Phase transition happened with enhanced doping content. Density results decreased with the higher waste content. The order degree of structure decreased as waste content increased. The sintered matrix represented considerable chemical stability.

研究领域: 材料科学 · 核废料处理
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2021 ·Vol. 46 ·期 4 ·4965-4974 · IF 5.164

Direct carbon solid oxide fuel cells powered by rice husk biochar

Weizi Cai,Xin Tong,Xiaomin Yan,Hualing Li,Yuzhi Li,Xinyu Gao,Yanning Guo,Weichuang Wu,Daishuang Fu,Xingkai Huang,Jiang Liu,Hailin Wang

Summary The inefficient application of fossil energy is one of the fundamental factors leading to global warming. Bioenergy is a renewable energy and also a carbon-neutral energy, with advantages of extensive sources, diverse products, and environmental friendliness. Direct carbon solid oxide fuel cell (DC-SOFC) is a novel high-efficient bioenergy technology, which is able to directly convert the chemical energy of biochar into power. A biochar derived from rice husk is applied to power an electrolyte-supported DC-SOFC. The maximum power density of the cell with pure rice husk biochar is 135 mW cm −2 at 850°C, which enhances to 214 mW cm −2 after using a Boudouard reaction catalyst. The microstructures, components and thermochemical parameters of the biochar are characterized and analyzed. The results show that the microstructure of the rice husk biochar is rough and porous. Na, K, Mg, Al, and other elements are found to present in the biochar. The physicochemical properties of the biochar and the enhanced electrical output of the DC-SOFCs are demonstrated and discussed in detail.

研究领域: 能源生物学 · 材料科学
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2022 ·Vol. 46 ·期 14 ·19686-19696 · IF 4.672

Self-supported Co, P-codoped MnCO3 pyramid as an efficient Electrocatalyst for hydrogen evolution reaction

Feng Wang,Yinrong Lv,Xueli Bai,Shengjian Zhang,Huifang Wang,Baoyi Li,Aifang Liu,Xiaoping Zhang

Summary Polyhydride electrocatalysts integrated directly into metal substrates have attracted attention because they can provide high electrochemical specific surface area and excellent mechanical properties. In this work, through the classical hydrothermal method and subsequent phosphating procedure, we synthesized for the first time an electrocatalyst with a pyramid-shaped MnCO 3 as the main structure, P and Co as co-doping elements, named Co, P-MnCO 3 , and used it as hydrogen evolution reaction (HER). The experimental results show that the excellent catalytic activity in alkaline media, with current densities of 10 and 200 mA∙cm −2 at 61 mV and 158 mV and low overpotentials, which are better than P-Co (108/234 mV) and P-MnCO 3 (175 mV/340 mV), etc. it has more electrochemically active sites, faster charge transfer rate and lower resistance. The excellent electrochemical properties benefit from the unique highly active binary Co, P-MnCO 3 pyramid brick sites shortened the ion transfer distance and optimized synergistic effect between the doped metal elements (Co,P between MnCO 3 ), the porous connection between Co, P-MnCO 3 and the high conductivity substrate, increased the electron-transfer efficiency between the substrate and material, accelerating the conversion of H + to H 2 ; facilitated the release of bubbles and provided excellent mechanical properties for improved catalyst stability. This work provides a new idea for the synthesis of multi-element electrocatalysts.

研究领域: 材料科学 · 电化学
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2020 ·Vol. 45 ·期 3 ·4396-4409 · IF 3.741

Investigation on preparation, thermal, and mechanical properties of carbon fiber decorated with hexagonal boron nitride/silicone rubber composites for battery thermal management

Zhenzhen Meng,Zhite Dai,Kai Chen,Shuangfeng Wang

Summary Adding thermally conductive filler to polymer matrix is a workable way to increase its thermal conductivity. In this work, carbon fiber (CF) and hexagonal boron nitride (h-BN) were employed to obtain hybrid fillers, firstly, (mh-BN@CF) by electrostatic self-assembly method, then added mh-BN@CF to silicone rubber (SR) matrix to prepare mh-BN@CF/SR composites. There was a good interface compatibility between mh-BN@CF and SR matrix. Besides, the composites can achieve best thermal conductivity when h-BN and CF are at the optimal fill ratio. When the mass ratio of h-BN:CF is7:3 and the filling content is 54 phr, the thermal conductivity of mh-BN@CF/SR can reach 1.3 W/(m K), and it is 23.7% and 400.4% larger than the mixed-filled h-BN/CF/SR composites and SR matrix, respectively. Simultaneously, the mh-BN@CF/SR composites also exhibited good electrical insulation, mechanical properties, and thermal stability. Finally, the prepared composites are used in a liquid-cooled battery thermal management system (BTMS). The effect of the composites on the performance of the BTMS is discussed by numerical method. The results show that the improved thermal conductivity of the composites can highly reduce the temperature of the battery cells. The prepared composites can highly enhance the performance of BTMS.

研究领域: 材料科学 · 能源工程
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2022 ·Vol. 46 ·期 14 ·19480-19492 · IF 4.672

Amino-functionalized SiO2 modified porous polyetherimide separator for high performance Li-S batteries

Jiuqing Liu,Fanli Zeng,Meng Liu,Junying He,Qihou Li,Feifei Song,Zikun Hong,Ya Chen,Lishun Bai,Chen Cheng,Zehao Chen

Summary As one of the most promising energy storage systems, the application of lithium sulfur battery is hindered by low ionic conductivity, poor thermal stability, and a serious shuttle effect of polysulfide species of commercial polyolefin separators. Herein, a kind of novel porous polyetherimide (PEI) based separator (IAPEI-4) with excellent heat resistance and electrochemical properties was prepared. Briefly, by grafting amino group (–NH 2 ) onto the surface of SiO 2 , highly dispersed amino-functionalized SiO 2 (A-SiO 2 ) were synthesized as fillers to blend PEI matrix. Based on physical characterizations of the representative IAPEI-4 separator, abundant micropores and mesopores exist in the separator, and A-SiO 2 nanoparticles are uniformly distributed in the PEI matrix. The ameliorated Li + transport channels and the uniform distribution of A-SiO 2 nanoparticles endow IAPEI-4 separator with higher ionic conductivity (1.60 mS cm −1 ) and Li + transfer number (0.63). Besides, the IAPEI-4 separator exhibits good electrochemical stability and excellent thermal stability (no shrinkage at 200°C). The Li-S cells with the IAPEI separator also show greatly enhanced electrochemical performances. After 100 cycles, its specific discharge capacity can reach 695.4 mAh g −1 at 0.2 C and its capacity retention rate is 84.8%. This simple and effective separator modification method can provide a general strategy to achieve high-performance Li-S batteries.

研究领域: 材料科学 · 能源存储技术
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2020 ·Vol. 45 ·期 5 ·6876-6887 · IF 3.741

Enhanced electrochemical properties and interfacial stability of poly(ethylene oxide) solid electrolyte incorporating nanostructured Li1.3Al0.3Ti1.7(PO4)3 fillers for all solid state lithium ion batteries

Erqing Zhao,Yudi Guo,Yuan Xin,Guangri Xu,Xiaowei Guo

Summary Poly(ethylene oxide) (PEO) polymer electrolyte has been regarded as a potential solid electrolyte which can be applied in all-solid-state lithium-ion batteries (ASSLIBs). Nevertheless, low electrochemical properties and poor electrolyte/Li anode interfacial stability hinder its further application. In our work, the Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 (LATP) nanomaterials with Nasicon structure have been synthesized using a simple solvent-thermal method, followed by being embedded into PEO polymer to form LATP filled PEO solid composite electrolytes. Effects of LATP content and particle size on electrochemical performances of solid electrolytes have been studied. By adjusting the calcination temperature, the uniformly distributed Nasicon-type LATP powders with different sizes can be obtained. The electrochemical properties of PEO polymer electrolyte have been effectively enhanced by filling LATP nanoparticles. The composite electrolyte filled with 5 wt% LATP particles calcined at 850°C exhibits a high ionic conductivity of 5.24×10 −4 S cm −1 at 55°C, which has a high electrochemical stability window of over 5 V versus Li/Li + and a superior interfacial stability with Li metal. A LiFePO 4 /Li ASSLIB fabricated with the optimum composite electrolyte shows the excellent rate capability, and its discharge capacities at 0.2C, 0.5C, 1C, and 2C are 151.97, 151.56, 145.51, and 128.02 mAh·g −1 . Moreover, the discharge capacity of the cell decreases from 151.69 to 130.53 mAh·g −1 after 100 charge-discharge cycles at 0.5C rate, and the corresponding capacity retention is 86.05%. These results demonstrate that LATP nanoparticles obtained via the solvent-thermal method are the alternative fillers for PEO polymer electrolyte.

✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2020 ·Vol. 45 ·期 4 ·5337-5346 · IF 3.741

Characterization of SrFe0.9-xCuxMo0.1O3-δ (x = 0, 0.1 and 0.2) as cathode for intermediate-temperature solid oxide fuel cells

Chuangang Yao,Jixing Yang,Haixia Zhang,Sigeng Chen,Jian Meng,Kedi Cai

Summary Cu doped perovskites SrFe 0.9- x Cu x Mo 0.1 O 3- δ (SFCM, x = 0-0.2) are explored as cathodes for IT-SOFCs. The influence of Cu doping on the property of SFCM series was studied in detail. The oxygen content decreases with the increase of Cu doping amount. SFCM samples are chemically compatible with LSGM electrolyte. However, the TEC values are still a bit higher than that of some common SOFC electrolytes. At 750°C, the R p values are 0.261, 0.227 and 0.155 Ω·cm 2 for SFCM0, SFCM0.1, and SFCM0.2. The obtained activation energies for x = 0, 0.1, and 0.2 are 1.01, 0.98, and 0.87 eV, respectively. These results indicate that Cu doping into SrFe 0.9- x Cu x Mo 0.1 O 3- δ has a favorable effect on the electrochemical activity of the materials.

研究领域: 材料科学 · 电化学 · 能源材料 · 固体氧化物燃料电池 · 无机功能材料
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2020 ·Vol. 45 ·期 4 ·5841-5851 · IF 3.741

Characterization and electrocatalytic properties of electrospun Pt-IrO2 nanofiber catalysts for oxygen evolution reaction

Zhi Ming Wang,Peng Liu,Yan Peng Cao,Feng Ye,Chao Xu,Xiao Ze Du

Summary In this study, novel Pt-IrO 2 nanofiber catalysts for oxygen evolution reaction (OER) were successfully prepared using the electrospinning method with a high-concentration precursor solution. The composition and structure of catalysts were characterized, and the electrocatalytic performance of the nanofiber catalysts in water electrolysis was investigated from various aspects such as overpotential, charge transfer resistance, and exchange current density. Special attention was paid on the effect of Pt/Ir ratio on the electrocatalytic activity of the electrospun nanofibers. The results showed that the Pt-IrO 2 nanofiber catalysts with average fiber diameters ranging from 10 to 100 nm can be successfully obtained by the electrospinning method, and the average diameter decreased with the increase of Pt content. Since a bigger amount of IrO 2 content and a thinner fiber structure are all beneficial to the electrocatalytic performance, the Pt-IrO 2 catalysts with Pt:Ir = 1:9 and Pt:Ir = 9:1 both showed better catalytic performance for OER than the commercial IrO 2 , which was also demonstrated by the lower charge transfer resistance and higher exchange current density. As a result, the overpotentials of Pt-IrO 2 catalysts with Pt:Ir = 1:9 and Pt:Ir = 9:1 are 50 mV and 32 mV lower than the overpotential of the commercial IrO 2 at 30 mA cm −2 in 0.5 M H 2 SO 4 , respectively. The electrospun Pt-IrO 2 nanofiber catalyst with proper Pt content seems to be very promising since it can not only improve the catalytic performance and the safety of PEM electrolysis cells, but also reduce the amount of more expensive Ir in catalysts.

研究领域: 材料科学 · 电化学 · 纳米材料 · 能源化学 · 催化化学
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2022 ·Vol. 46 ·期 11 ·16075-16081 · IF 4.672

A hollow structure for flow and bendable paper-based zinc-air battery

Yang Yang,Haoran Zhang,Xun Zhu,Dingding Ye,Rong Chen,Qiang Liao

Summary Tremendous research has focused on the wearable electronic device, leading to the basic requirement of suitable power sources. Herein, we report one bendable paper-based zinc-air battery with a novel hollow channel structure. It achieves a maximum power density of 138 mW/cm 2 , outperforming the state-of-art paper-based batteries reported previously. The boosted performance is assigned to the low charge transfer resistance and facilitated mass transfer from the hollow structure. It demonstrates the positive design of microchannel structure is profitable for the power-generation enhancement, and offers a possible route to commercialize the paper-based power generators.

研究领域: 电化学能源 · 柔性电子学 · 材料科学 · 纳米能源 · 生物医学工程
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH · 2019 ·Vol. 43 ·期 10 ·5355-5366 · IF 3.343

Electrospun porous Fe2O3 nanotubes as counter electrodes for dye-sensitized solar cells

Chenle Zhang,Peixin Zhang,Han Zhang

Summary Porous Fe 2 O 3 nanostructures were synthesized through electrospinning of Fe (NO 3 ) 3 /polyvinylpyrrolidone followed by calcination in air. The morphology of the resultant Fe 2 O 3 was tuned by changing the ratio between Fe (NO 3 ) 3 and the polymer matrix. The performance of these nanostructures as counter electrodes in dye-sensitized solar cells (DSSCs) was investigated. It was found that nanotubes exhibit significantly higher catalytic efficiency toward reducing I − /I 3 − electrolytes than nanorods and nanobelts, showing a photoelectric conversion efficiency of 4.0%, also superior to a range of transition metal oxides. Furthermore, the nanotube-based counter electrode showed lower resistance than other Fe 2 O 3 nanostructures. These results were attributed to the high specific surface area (90.2 m 2 g −1 ) of the nanotubes, which provides a large reaction site and can promote the charge transfer at the electrode/electrolyte interfaces. The low cost and ease of mass production make Fe 2 O 3 nanotube a promising candidate to replace Pt as the counter electrode in DSSCs.

研究领域: 材料科学 · 纳米技术 · 可再生能源 · 太阳能电池
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