Ekaterina V. Astrova, Irina Yu Sapurina, Alesya V. Parfeneva, Galina V. Li, Alexey V. Nashchekin, Darina A. Lozhkina, Aleksander M. Rumyantsev
The properties of lithium-ion battery (LIB) anodes fabricated from nanoscale silicon Si and polyaniline (PANI) as a binder are reported. PANI is prepared by in situ polymerization of aniline in the presence of phytic acid, which serves both as dopant and as a gel-forming agent. PANI pellets obtained by dry compression are used to investigate the morphology and to measure the resistivity of PANI and Si/PANI composites. The anodes are fabricated using the slurry technique. Their properties as a function of precursor ratio are studied in the half-cell cells by charge–discharge characteristics, cyclic voltammetry, electrochemical impedance spectroscopy and cyclic lifetime. It is shown that stable cycling (>350 cycles at a current of 300 mA g−1) is inherent only to thin Si/PANI layers with composite loading <0.7 mg cm−2. The discharge capacity in this case is as high as 500–800 mAh g−1.
报告了用纳米级硅 Si 和聚苯胺 (PANI) 作为粘合剂制造的锂离子电池 (LIB) 阳极的特性。PANI 是在植酸存在下通过苯胺原位聚合制备的,植酸既是掺杂剂,也是凝胶形成剂。通过干压获得的 PANI 颗粒用于研究 PANI 和 Si/PANI 复合材料的形态并测量其电阻率。阳极采用浆料技术制造。在半电池中,通过充放电特性、循环伏安法、电化学阻抗光谱法和循环寿命,研究了它们作为前驱体比率函数的特性。结果表明,只有复合负载为 0.7 mg cm-2 的薄 Si/PANI 层才能实现稳定循环(电流为 300 mA g-1 时循环 350 次)。这种情况下的放电容量高达 500-800 mAh g-1。
{"title":"Nanocomposites for Lithium-Ion Battery Anodes Made of Silicon and Polyaniline Doped with Phytic Acid","authors":"Ekaterina V. Astrova, Irina Yu Sapurina, Alesya V. Parfeneva, Galina V. Li, Alexey V. Nashchekin, Darina A. Lozhkina, Aleksander M. Rumyantsev","doi":"10.1002/ente.202401156","DOIUrl":"10.1002/ente.202401156","url":null,"abstract":"<p>The properties of lithium-ion battery (LIB) anodes fabricated from nanoscale silicon Si and polyaniline (PANI) as a binder are reported. PANI is prepared by in situ polymerization of aniline in the presence of phytic acid, which serves both as dopant and as a gel-forming agent. PANI pellets obtained by dry compression are used to investigate the morphology and to measure the resistivity of PANI and Si/PANI composites. The anodes are fabricated using the slurry technique. Their properties as a function of precursor ratio are studied in the half-cell cells by charge–discharge characteristics, cyclic voltammetry, electrochemical impedance spectroscopy and cyclic lifetime. It is shown that stable cycling (>350 cycles at a current of 300 mA g<sup>−1</sup>) is inherent only to thin Si/PANI layers with composite loading <0.7 mg cm<sup>−2</sup>. The discharge capacity in this case is as high as 500–800 mAh g<sup>−1</sup>.</p>","PeriodicalId":11573,"journal":{"name":"Energy technology","volume":"12 11","pages":""},"PeriodicalIF":3.6,"publicationDate":"2024-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142195758","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The present status of wavelength‐selective transparent photovoltaic (TPV) devices for green buildings and self‐powered wireless sensors is comprehensively reviewed. Photoactive absorbers for both UV and near‐infrared (NIR)‐selective TPV are discussed. UV‐selective devices based on engineered small organic molecules have demonstrated high transparency (>80%). However, their power conversion efficiency (PCE) is ≈1%. Higher PCE of 3.15% and transparency of 51.4% are obtained from the bulk heterojunction (BHJ) of a wide energy gap conjugated polymer and nonfullerene acceptor (NFA). The highest transparency of 84.6% together with device stability and scalability is realized for CsPbCl2.5Br0.5 perovskite absorbers. The few reported NIR‐selective TPV devices are all organic solar cells. Using BHJs comprising ultranarrow energy gap conjugated polymer and NFA, a PCE of 5.74% and transparency of ≈60% can be obtained. However, current IR‐selective devices are generally limited by an absorption tail that encroaches into the visible region and result in suboptimal color rendering. To address this, a new spectral range ratio (SRR) parameter is proposed to classify absorbers for IR‐selective TPV devices. A molecular design strategy to increase the SRR based on frontier molecular orbital theory is outlined.
{"title":"Organic and Inorganic Photoactive Absorbers for Wavelength‐Selective Transparent Photovoltaic Devices: Focus Review","authors":"Terence K. S. Wong","doi":"10.1002/ente.202400961","DOIUrl":"https://doi.org/10.1002/ente.202400961","url":null,"abstract":"The present status of wavelength‐selective transparent photovoltaic (TPV) devices for green buildings and self‐powered wireless sensors is comprehensively reviewed. Photoactive absorbers for both UV and near‐infrared (NIR)‐selective TPV are discussed. UV‐selective devices based on engineered small organic molecules have demonstrated high transparency (>80%). However, their power conversion efficiency (PCE) is ≈1%. Higher PCE of 3.15% and transparency of 51.4% are obtained from the bulk heterojunction (BHJ) of a wide energy gap conjugated polymer and nonfullerene acceptor (NFA). The highest transparency of 84.6% together with device stability and scalability is realized for CsPbCl<jats:sub>2.5</jats:sub>Br<jats:sub>0.5</jats:sub> perovskite absorbers. The few reported NIR‐selective TPV devices are all organic solar cells. Using BHJs comprising ultranarrow energy gap conjugated polymer and NFA, a PCE of 5.74% and transparency of ≈60% can be obtained. However, current IR‐selective devices are generally limited by an absorption tail that encroaches into the visible region and result in suboptimal color rendering. To address this, a new spectral range ratio (SRR) parameter is proposed to classify absorbers for IR‐selective TPV devices. A molecular design strategy to increase the SRR based on frontier molecular orbital theory is outlined.","PeriodicalId":11573,"journal":{"name":"Energy technology","volume":"26 1","pages":""},"PeriodicalIF":3.8,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142195689","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ang Li, Chengliang Fan, Hongjie Tang, Zutao Zhang, Genshuo Liu, Linyang He, Jie Zhao, Jianhong Zhou, Yongli Hu
Safety monitoring sensors in smart railways need a sustainable onboard power supply. This article proposes a counter-rotating gear energy harvester (CG-EH) to convert the longitudinal vibration energy of trains into electricity for onboard sensors.CG-EH consists of a vibration input module, a motion conversion module, and an energy conversion module. The vibration input module converts the longitudinal displacement of the coupler into the rotational motion of the gears. The motion conversion module realizes the conversion of the reciprocating input displacement into the unidirectional rotation based on a counter-rotating gear set, multi-stage spur gear sets can effectively mitigate the effects of excitation on CG-EH. The energy conversion module transforms the kinetic energy of the unidirectional rotation into electrical energy through a generator. Experimental results show that the energy outputs of CG-EH are improved with longitudinal vibration compared with the usual onboard energy harvester. From the result, the peak output power of CG-EH is 14.59 W, the peak efficiency reaches 39.2%, enough to power relevant onboard sensors. Moreover, CG-EH can monitor the running status of trains based on deep learning. From the experiment results and application prospects, CG-EH is a favorable solution for the power supply problems of onboard sensors in smart railways.
{"title":"Smart Railway Transportation: Self-Powered and Self-Sensing Vibration Energy Harvester","authors":"Ang Li, Chengliang Fan, Hongjie Tang, Zutao Zhang, Genshuo Liu, Linyang He, Jie Zhao, Jianhong Zhou, Yongli Hu","doi":"10.1002/ente.202401253","DOIUrl":"10.1002/ente.202401253","url":null,"abstract":"<p>Safety monitoring sensors in smart railways need a sustainable onboard power supply. This article proposes a counter-rotating gear energy harvester (CG-EH) to convert the longitudinal vibration energy of trains into electricity for onboard sensors.CG-EH consists of a vibration input module, a motion conversion module, and an energy conversion module. The vibration input module converts the longitudinal displacement of the coupler into the rotational motion of the gears. The motion conversion module realizes the conversion of the reciprocating input displacement into the unidirectional rotation based on a counter-rotating gear set, multi-stage spur gear sets can effectively mitigate the effects of excitation on CG-EH. The energy conversion module transforms the kinetic energy of the unidirectional rotation into electrical energy through a generator. Experimental results show that the energy outputs of CG-EH are improved with longitudinal vibration compared with the usual onboard energy harvester. From the result, the peak output power of CG-EH is 14.59 W, the peak efficiency reaches 39.2%, enough to power relevant onboard sensors. Moreover, CG-EH can monitor the running status of trains based on deep learning. From the experiment results and application prospects, CG-EH is a favorable solution for the power supply problems of onboard sensors in smart railways.</p>","PeriodicalId":11573,"journal":{"name":"Energy technology","volume":"12 12","pages":""},"PeriodicalIF":3.6,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142195688","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This study assesses the mechanical, thermal, and dielectric properties, as well as the conductivity and water contact angle, of eco-friendly polyethylene oxide (PEO) and aluminium oxyhydroxide (AlOOH) films prepared using water as a green solvent for fabricating flexible nanodielectric devices. X-ray diffraction and Fourier transform infrared analysis confirm the presence of AlOOH in the nanocomposites. Field emission scanning electron microscopy analysis reveals the surface morphology of nanocomposites, showing a more uniform distribution of AlOOH nanoparticles at 5 and 7 wt% loading. The influence of nanofiller content on the thermal properties of films is evaluated by differential scanning calorimetry and thermogravimetric analysis. Increasing AlOOH content significantly enhances both the glass transition temperature and the thermal stability of PEO/AlOOH nanocomposites. The films exhibit improved mechanical properties, with a tensile strength of 31.11 MPa and Young's modulus of 339 MPa at 5 wt% AlOOH. Electrical conductivity, dielectric parameters, and complex impedance are measured for all films. The PEO with 7 wt% AlOOH shows optimal electrical conductivity and dielectric constant. These findings suggest that altering AlOOH concentrations enables fine-tuning of the thermal, mechanical, and electrical properties of nanocomposite films. This versatility offers great potential for developing advanced flexible organoelectronic devices and nanodielectric materials.
{"title":"Eco-Friendly Polyethylene Oxide/Aluminum Oxyhydroxide Nanocomposites for Flexible Energy Storage Devices","authors":"Meera Krishnan, Manammel Thankappan Ramesan","doi":"10.1002/ente.202401416","DOIUrl":"10.1002/ente.202401416","url":null,"abstract":"<p>This study assesses the mechanical, thermal, and dielectric properties, as well as the conductivity and water contact angle, of eco-friendly polyethylene oxide (PEO) and aluminium oxyhydroxide (AlOOH) films prepared using water as a green solvent for fabricating flexible nanodielectric devices. X-ray diffraction and Fourier transform infrared analysis confirm the presence of AlOOH in the nanocomposites. Field emission scanning electron microscopy analysis reveals the surface morphology of nanocomposites, showing a more uniform distribution of AlOOH nanoparticles at 5 and 7 wt% loading. The influence of nanofiller content on the thermal properties of films is evaluated by differential scanning calorimetry and thermogravimetric analysis. Increasing AlOOH content significantly enhances both the glass transition temperature and the thermal stability of PEO/AlOOH nanocomposites. The films exhibit improved mechanical properties, with a tensile strength of 31.11 MPa and Young's modulus of 339 MPa at 5 wt% AlOOH. Electrical conductivity, dielectric parameters, and complex impedance are measured for all films. The PEO with 7 wt% AlOOH shows optimal electrical conductivity and dielectric constant. These findings suggest that altering AlOOH concentrations enables fine-tuning of the thermal, mechanical, and electrical properties of nanocomposite films. This versatility offers great potential for developing advanced flexible organoelectronic devices and nanodielectric materials.</p>","PeriodicalId":11573,"journal":{"name":"Energy technology","volume":"12 12","pages":""},"PeriodicalIF":3.6,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142195690","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jitendra Kumar Yadav, Bharti Rani, Priyanka Saini, Ambesh Dixit
Owing to iron's natural abundance, low cost, and affordability, nonaqueous rechargeable iron-ion (Fe-ion) batteries have the potential for alternative rechargeable energy-storage devices. However, developing cathodes with adequate superior Fe2+ storage during charge–discharge is a major challenge. Herein, V2O5 porous microspheres (V2O5–PMS) are synthesized as efficient cathodes due to their unique characteristics, including high surface area and large interlayer spacing, which provide high electrochemical performance and fast charge kinetics. The nonaqueous Fe-ion battery is fabricated under ambient conditions using mild steel as an anode and a V2O5–PMS cathode. The cyclic voltammetry measurements suggests a high diffusion coefficient of Fe2+ ions in the redox process during charge–discharge. The V2O5–PMS-based cathode shows ≈205 mAh g−1 gravimetric capacity at 33 and ≈70 mAh g−1 at 1 A g−1 (≈15 C). It exhibits capacity retention of ≈70% in 600 cycles at a very high current rate of 3 A g−1. The impedance spectroscopy measurements are carried out between the cell's cycling to understand the electrode–electrolyte interface resistance over cycling. The four CR-2032 coin cells are assembled in series to glow a white and red light-emitting diode to demonstrate its potential as an alternative energy-storage system.
由于铁的天然丰富性、低成本和可负担性,非水可充电铁离子(Fe-ion)电池具有替代可充电储能设备的潜力。然而,开发在充放电过程中具有足够出色的 Fe2+ 储存能力的阴极是一项重大挑战。在此,我们合成了 V2O5 多孔微球(V2O5-PMS)作为高效阴极,因为它们具有独特的特性,包括高比表面积和大的层间间距,可提供高电化学性能和快速充电动力学。利用低碳钢作为阳极和 V2O5-PMS 阴极,在环境条件下制造出了非水铁离子电池。循环伏安法测量结果表明,在充放电的氧化还原过程中,Fe2+ 离子的扩散系数很高。基于 V2O5-PMS 的阴极在 33 摄氏度时的重力容量≈205 mAh g-1,在 1 A g-1(≈15 C)时的重力容量≈70 mAh g-1。在 3 A g-1 的极高电流速率下循环 600 次,其容量保持率≈70%。阻抗光谱测量在电池循环之间进行,以了解循环过程中电极-电解质界面电阻的变化。将四个 CR-2032 纽扣电池串联起来,使白色和红色发光二极管发光,以展示其作为替代能源存储系统的潜力。
{"title":"A High-Performance and Fast-Charging Rechargeable Iron-Ion Battery Using V2O5 Porous Microspheres Cathode","authors":"Jitendra Kumar Yadav, Bharti Rani, Priyanka Saini, Ambesh Dixit","doi":"10.1002/ente.202401334","DOIUrl":"10.1002/ente.202401334","url":null,"abstract":"<p>Owing to iron's natural abundance, low cost, and affordability, nonaqueous rechargeable iron-ion (Fe-ion) batteries have the potential for alternative rechargeable energy-storage devices. However, developing cathodes with adequate superior Fe<sup>2+</sup> storage during charge–discharge is a major challenge. Herein, V<sub>2</sub>O<sub>5</sub> porous microspheres (V<sub>2</sub>O<sub>5</sub>–PMS) are synthesized as efficient cathodes due to their unique characteristics, including high surface area and large interlayer spacing, which provide high electrochemical performance and fast charge kinetics. The nonaqueous Fe-ion battery is fabricated under ambient conditions using mild steel as an anode and a V<sub>2</sub>O<sub>5</sub>–PMS cathode. The cyclic voltammetry measurements suggests a high diffusion coefficient of Fe<sup>2+</sup> ions in the redox process during charge–discharge. The V<sub>2</sub>O<sub>5</sub>–PMS-based cathode shows ≈205 mAh g<sup>−1</sup> gravimetric capacity at 33 and ≈70 mAh g<sup>−1</sup> at 1 A g<sup>−1</sup> (≈15 C). It exhibits capacity retention of ≈70% in 600 cycles at a very high current rate of 3 A g<sup>−1</sup>. The impedance spectroscopy measurements are carried out between the cell's cycling to understand the electrode–electrolyte interface resistance over cycling. The four CR-2032 coin cells are assembled in series to glow a white and red light-emitting diode to demonstrate its potential as an alternative energy-storage system.</p>","PeriodicalId":11573,"journal":{"name":"Energy technology","volume":"12 12","pages":""},"PeriodicalIF":3.6,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142195691","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Apri Wiyono, Nurin Wahidah Mohd Zulkifli, Wan Mohd Ashri Wan Daud, Yusep Sukrawan, Rani Anggrainy, Ade Syafrinaldy, Henry Nolandy, Asroful Abidin, Ragil Sukarno, Muhammad Aziz
Biomass can be converted into carbon through carbonization processes (pyrolysis and hydrothermal carbonization) and activation (physical and chemical). The resulting carbon has a high potential as a supercapacitor electrode material due to its porous structure, which supports rapid ion transport. Various methods have been developed to extract or transform biomass into porous carbon. One of the newly developed nanocarbon materials is carbon nanotubes (CNTs) because they have advantages in terms of mechanical, physical, chemical, and electrical properties. This review discusses various kinds of CNT synthesis as activated carbon composites for supercapacitors. The synthesis of these CNTs can be conducted through chemical and physical methods, including arc discharge, laser vaporization, and chemical vapor deposition (CVD). This work reviews various methods of CNT synthesis and analyzes the best methods to be used as composites for supercapacitors for electric vehicles. It is concluded that CVD is the best method for synthesizing CNTs. Its main advantage is that CNTs can be used directly without purification unless the catalyst particles need to be removed. However, further experimental studies are required to find the most optimal conditions for each composite from a type of mesoporous activated carbon and CNTs in terms of preparation and performance outcome.
{"title":"Review on Synthesis Methods of Carbon Nanotubes as Activated Carbon Composites Based on Biomass for Supercapacitors in Electric Vehicles","authors":"Apri Wiyono, Nurin Wahidah Mohd Zulkifli, Wan Mohd Ashri Wan Daud, Yusep Sukrawan, Rani Anggrainy, Ade Syafrinaldy, Henry Nolandy, Asroful Abidin, Ragil Sukarno, Muhammad Aziz","doi":"10.1002/ente.202401228","DOIUrl":"https://doi.org/10.1002/ente.202401228","url":null,"abstract":"Biomass can be converted into carbon through carbonization processes (pyrolysis and hydrothermal carbonization) and activation (physical and chemical). The resulting carbon has a high potential as a supercapacitor electrode material due to its porous structure, which supports rapid ion transport. Various methods have been developed to extract or transform biomass into porous carbon. One of the newly developed nanocarbon materials is carbon nanotubes (CNTs) because they have advantages in terms of mechanical, physical, chemical, and electrical properties. This review discusses various kinds of CNT synthesis as activated carbon composites for supercapacitors. The synthesis of these CNTs can be conducted through chemical and physical methods, including arc discharge, laser vaporization, and chemical vapor deposition (CVD). This work reviews various methods of CNT synthesis and analyzes the best methods to be used as composites for supercapacitors for electric vehicles. It is concluded that CVD is the best method for synthesizing CNTs. Its main advantage is that CNTs can be used directly without purification unless the catalyst particles need to be removed. However, further experimental studies are required to find the most optimal conditions for each composite from a type of mesoporous activated carbon and CNTs in terms of preparation and performance outcome.","PeriodicalId":11573,"journal":{"name":"Energy technology","volume":"38 1","pages":""},"PeriodicalIF":3.8,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142195759","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tutku Mutlu-Cetinkaya, Serap Hayat Soytas, Rezan Demir-Cakan
Li–Se batteries are promising energy storage systems due to the high theoretical volumetric capacity and electrical conductivity of selenium. However, the formation of dissolved polyselenide in ether-based electrolytes is one of the main factors affecting the electrochemical performance of Li–Se batteries. Herein, the presence and solubility of polyselenides in ether-based electrolytes are initially investigated using UV–vis spectroscopy and compared with carbonate-based solvents. Then, to address the polyselenide shuttle effect, SnCl2-containing poly(acrylonitrile-co-vinylpyrrolidone) (oPANVP/SnCl2) nanofibrous interlayer is utilized to retain the dissolved compounds. The absorption capacity of this interlayer is investigated and quantitatively demonstrated by UV–vis spectroscopy. The cell with the interlayer achieves a discharge capacity of 266 mAh g−1 after 150 cycles, significantly higher than the cell without the interlayer. Furthermore, 3-electrode electrochemical impedance spectroscopy and open-circuit voltage monitoring are conducted to investigate the impact of the oPANVP/SnCl2 interlayer on the solubility of polyselenides. The improved electrochemical results indicate that ether-based electrolytes can be successfully utilized in Li–Se batteries when an effective interlayer is present to adsorb polyselenides.
由于硒具有较高的理论容量和导电性,锂-硒电池是一种前景广阔的储能系统。然而,在醚基电解质中形成溶解的多硒化物是影响硒化锂电池电化学性能的主要因素之一。本文首先使用紫外可见光谱法研究了多硒化物在醚基电解质中的存在和溶解度,并与碳酸盐基溶剂进行了比较。然后,为了解决多硒化物的穿梭效应,利用含有氯化锡的聚丙烯腈-乙烯基吡咯烷酮(oPANVP/SnCl2)纳米纤维夹层来保留溶解的化合物。该夹层的吸收能力通过紫外可见光谱进行了研究和定量证明。带有中间膜的电池在循环 150 次后,放电容量达到 266 mAh g-1,明显高于不带中间膜的电池。此外,还进行了三电极电化学阻抗谱分析和开路电压监测,以研究 oPANVP/SnCl2 中间膜对多硒化物溶解度的影响。改进后的电化学结果表明,如果存在有效吸附多硒化物的中间层,醚基电解质可成功用于锂硒电池。
{"title":"Targeting the Dissolution of Polyselenides: An Investigation Involving UV–Vis Spectroscopy and Interlayer Development","authors":"Tutku Mutlu-Cetinkaya, Serap Hayat Soytas, Rezan Demir-Cakan","doi":"10.1002/ente.202401187","DOIUrl":"10.1002/ente.202401187","url":null,"abstract":"<p>Li–Se batteries are promising energy storage systems due to the high theoretical volumetric capacity and electrical conductivity of selenium. However, the formation of dissolved polyselenide in ether-based electrolytes is one of the main factors affecting the electrochemical performance of Li–Se batteries. Herein, the presence and solubility of polyselenides in ether-based electrolytes are initially investigated using UV–vis spectroscopy and compared with carbonate-based solvents. Then, to address the polyselenide shuttle effect, SnCl<sub>2</sub>-containing poly(acrylonitrile-co-vinylpyrrolidone) (oPANVP/SnCl<sub>2</sub>) nanofibrous interlayer is utilized to retain the dissolved compounds. The absorption capacity of this interlayer is investigated and quantitatively demonstrated by UV–vis spectroscopy. The cell with the interlayer achieves a discharge capacity of 266 mAh g<sup>−1</sup> after 150 cycles, significantly higher than the cell without the interlayer. Furthermore, 3-electrode electrochemical impedance spectroscopy and open-circuit voltage monitoring are conducted to investigate the impact of the oPANVP/SnCl<sub>2</sub> interlayer on the solubility of polyselenides. The improved electrochemical results indicate that ether-based electrolytes can be successfully utilized in Li–Se batteries when an effective interlayer is present to adsorb polyselenides.</p>","PeriodicalId":11573,"journal":{"name":"Energy technology","volume":"12 12","pages":""},"PeriodicalIF":3.6,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142195692","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Liying Wang, Yu Zhao, Dun Lin, Qiming Wang, Chenguang Liu, Pan Chu, Puiki Leung
This study introduces a novel approach through the design and creation of a composite electrode, uniquely made of three distinct layers of micro/mesoporous electrospun carbon nanofiber (CNF) mats, featuring a gradient in pore size. This innovative gradient pore structure merges the benefits of varying pore sizes, significantly enhancing redox flow battery (RFB) efficiency. The first layer, a microporous CNF mat situated near the membrane, offers an extensive reactive surface area, minimizing charge transfer resistance and speeding up electrochemical reactions—key factors in enhancing battery reaction efficiency. The next layer, a mesoporous CNF mat, fine-tunes the flow properties of the electrolyte, lowering flow resistance while ensuring superior charge transfer capabilities. This structured gradient in pore size not only facilitates improved electrolyte penetration and even distribution but also harmonizes the balance between charge transfer efficiency and electrolyte flow, thus mitigating energy losses without compromising reaction velocity. Charge–discharge testing demonstrated notable performance gains: an energy efficiency of 82% at 100 mA cm−2 (surpassing traditional electrodes by 71.5%) and 69% at 200 mA cm−2, alongside a 77.4% increase in peak power density. This advancement not only enhances energy and power densities but also its lifespan, marking a significant step forward for RFB technologies.
本研究通过设计和制造一种复合电极引入了一种新方法,这种电极由三层独特的微/多孔电纺碳纳米纤维(CNF)毡组成,具有孔径梯度。这种创新的梯度孔结构融合了不同孔径的优点,显著提高了氧化还原液流电池(RFB)的效率。第一层是位于膜附近的微孔 CNF 垫,提供了广泛的反应表面积,最大限度地减少了电荷转移阻力,加快了电化学反应--这是提高电池反应效率的关键因素。下一层是介孔 CNF 毡,可微调电解质的流动特性,降低流动阻力,同时确保卓越的电荷转移能力。这种结构化的孔径梯度不仅有助于改善电解液的渗透和均匀分布,还能协调电荷转移效率和电解液流动之间的平衡,从而在不影响反应速度的情况下减少能量损失。充放电测试显示了显著的性能提升:100 mA cm-2 时的能量效率为 82%(超过传统电极 71.5%),200 mA cm-2 时的能量效率为 69%,峰值功率密度提高了 77.4%。这一进步不仅提高了能量和功率密度,还延长了使用寿命,标志着 RFB 技术向前迈进了一大步。
{"title":"Electrospun Carbon Nanofiber Composite Electrode with Gradient Porous Structure for Rapid Ion Transport in an All-Vanadium Redox Flow Battery","authors":"Liying Wang, Yu Zhao, Dun Lin, Qiming Wang, Chenguang Liu, Pan Chu, Puiki Leung","doi":"10.1002/ente.202400825","DOIUrl":"10.1002/ente.202400825","url":null,"abstract":"<p>This study introduces a novel approach through the design and creation of a composite electrode, uniquely made of three distinct layers of micro/mesoporous electrospun carbon nanofiber (CNF) mats, featuring a gradient in pore size. This innovative gradient pore structure merges the benefits of varying pore sizes, significantly enhancing redox flow battery (RFB) efficiency. The first layer, a microporous CNF mat situated near the membrane, offers an extensive reactive surface area, minimizing charge transfer resistance and speeding up electrochemical reactions—key factors in enhancing battery reaction efficiency. The next layer, a mesoporous CNF mat, fine-tunes the flow properties of the electrolyte, lowering flow resistance while ensuring superior charge transfer capabilities. This structured gradient in pore size not only facilitates improved electrolyte penetration and even distribution but also harmonizes the balance between charge transfer efficiency and electrolyte flow, thus mitigating energy losses without compromising reaction velocity. Charge–discharge testing demonstrated notable performance gains: an energy efficiency of 82% at 100 mA cm<sup>−2</sup> (surpassing traditional electrodes by 71.5%) and 69% at 200 mA cm<sup>−2</sup>, alongside a 77.4% increase in peak power density. This advancement not only enhances energy and power densities but also its lifespan, marking a significant step forward for RFB technologies.</p>","PeriodicalId":11573,"journal":{"name":"Energy technology","volume":"12 10","pages":""},"PeriodicalIF":3.6,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142195761","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Thermal runaway propagation (TRP) in lithium batteries poses significant risks to energy-storage systems. Therefore, it is necessary to incorporate insulating materials between the batteries to prevent the TRP. However, the incorporation of insulating materials will impact the battery thermal management system (BTMS). In this article, the influence of aerogel insulation on liquid-cooled BTMS is analyzed employing experiments and simulations. In the experiment results, it is revealed that aerogel reduces heat dissipation from liquid-cooled battery packs, leading to elevated peak temperatures and steeper temperature gradients. Simulation of battery pack discharge warming based on the 3D model shows that the result matches very well with that in the experiment., indicating a maximum temperature rise from 34.92 to 42.57 °C at 2C when aerogel thickness is increased to 5 mm, alongside a temperature differential expansion from 11.11 to 17.50 °C. Nonetheless, beyond 3 mm thickness, further increases in aerogel thickness cause negligible (<0.1 °C) temperature alterations, defining the saturation thickness of aerogel. Furthermore, maintaining consistent thickness and stacking more aerogel layers do not mitigate its detrimental effects. Interestingly, augmenting the battery's through-thickness thermal conductivity counteracts the adverse outcomes of aerogel usage.
{"title":"Impact of Aerogel Barrier on Liquid-Cooled Lithium-Ion Battery Thermal Management System's Cooling Efficiency","authors":"Keyi Zeng, Ying Zhang, Liyu Tian, Zengyan Lai, Liang Zhu, Chuyuan Ma","doi":"10.1002/ente.202400923","DOIUrl":"10.1002/ente.202400923","url":null,"abstract":"<p>Thermal runaway propagation (TRP) in lithium batteries poses significant risks to energy-storage systems. Therefore, it is necessary to incorporate insulating materials between the batteries to prevent the TRP. However, the incorporation of insulating materials will impact the battery thermal management system (BTMS). In this article, the influence of aerogel insulation on liquid-cooled BTMS is analyzed employing experiments and simulations. In the experiment results, it is revealed that aerogel reduces heat dissipation from liquid-cooled battery packs, leading to elevated peak temperatures and steeper temperature gradients. Simulation of battery pack discharge warming based on the 3D model shows that the result matches very well with that in the experiment., indicating a maximum temperature rise from 34.92 to 42.57 °C at 2C when aerogel thickness is increased to 5 mm, alongside a temperature differential expansion from 11.11 to 17.50 °C. Nonetheless, beyond 3 mm thickness, further increases in aerogel thickness cause negligible (<0.1 °C) temperature alterations, defining the saturation thickness of aerogel. Furthermore, maintaining consistent thickness and stacking more aerogel layers do not mitigate its detrimental effects. Interestingly, augmenting the battery's through-thickness thermal conductivity counteracts the adverse outcomes of aerogel usage.</p>","PeriodicalId":11573,"journal":{"name":"Energy technology","volume":"12 11","pages":""},"PeriodicalIF":3.6,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142195693","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The presented maiden experimental study introduces a novel cell position concept for a modified reversible polymer electrolyte membrane fuel cell with an integrated hydrogen storage (H-storage) electrode. The primary focus of the current study is to enhance the H-storage capacity of a carbon-based self-standing electrode by testing it in vertical, horizontally upward, and horizontally downward positions to meet U.S. Department of Energy objectives. The results show that the developed cell achieves the highest electrochemical hydrogen adsorption (H-adsorption) of 1.3 weight percent (wt%) in the horizontal downward position during charging, surpassing the vertical position by 36.1% and outperforming the horizontal upward position by 25.3%. The reversible rates of stored hydrogen are measured as 0.587 wt% in the vertical position, 0.781 wt% in the horizontal upward position, and 0.998 wt% in the horizontal downward position. The cell manages to deliver a peak output of 2.2 V and a maximum current of 0.5 mA during the initial discharging phase. The insights gained from this study on cell positioning are poised to inspire future research efforts aimed at enhancing hydrogen storage capacity and its reversibility.
这项首次实验研究为带有集成储氢(H-storage)电极的改良型可逆聚合物电解质膜燃料电池引入了一种新的电池位置概念。当前研究的主要重点是通过在垂直、水平向上和水平向下位置进行测试,提高碳基自立式电极的储氢能力,以实现美国能源部的目标。结果表明,所开发的电池在水平向下位置充电时的电化学吸氢率(H-adsorption)最高,达到 1.3 重量百分比(wt%),比垂直位置高出 36.1%,比水平向上位置高出 25.3%。据测量,垂直位置的可逆储氢率为 0.587 重量%,水平向上位置为 0.781 重量%,水平向下位置为 0.998 重量%。在初始放电阶段,电池能输出 2.2 V 的峰值电压和 0.5 mA 的最大电流。这项研究在电池定位方面获得的启示,将激励未来旨在提高储氢能力及其可逆性的研究工作。
{"title":"Unlocking the Impact of “Cell Position” on Solid-State Hydrogen Storage: Investigations on an Activated Carbon Electrode Integrated in a Modified Reversible Polymer Electrolyte Membrane Fuel Cell","authors":"Rupinder Singh, Amandeep Singh Oberoi, Talwinder Singh","doi":"10.1002/ente.202400215","DOIUrl":"10.1002/ente.202400215","url":null,"abstract":"<p>The presented maiden experimental study introduces a novel cell position concept for a modified reversible polymer electrolyte membrane fuel cell with an integrated hydrogen storage (H-storage) electrode. The primary focus of the current study is to enhance the H-storage capacity of a carbon-based self-standing electrode by testing it in vertical, horizontally upward, and horizontally downward positions to meet U.S. Department of Energy objectives. The results show that the developed cell achieves the highest electrochemical hydrogen adsorption (H-adsorption) of 1.3 weight percent (wt%) in the horizontal downward position during charging, surpassing the vertical position by 36.1% and outperforming the horizontal upward position by 25.3%. The reversible rates of stored hydrogen are measured as 0.587 wt% in the vertical position, 0.781 wt% in the horizontal upward position, and 0.998 wt% in the horizontal downward position. The cell manages to deliver a peak output of 2.2 V and a maximum current of 0.5 mA during the initial discharging phase. The insights gained from this study on cell positioning are poised to inspire future research efforts aimed at enhancing hydrogen storage capacity and its reversibility.</p>","PeriodicalId":11573,"journal":{"name":"Energy technology","volume":"12 11","pages":""},"PeriodicalIF":3.6,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142195764","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}