CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Yang Bai,Yanbiao Zhao,Weidong Li,Linghui Meng,Yongping Bai,Guorong Chen
The developing sulfide solid electrolyte is a promising way to overcome shuttle effect of polysulfide in the traditional liquid Li-S battery. However, an air stable sulfide solid electrolyte and competitive solid–solid interface structure must be constructed firstly. Herein, we have designed an organic–inorganic multi-scale composite electrolytes to overcome the interfacial issues of solid state Li-S batteries (SSLSBs). The organic–inorganic composite electrolyte consists of a gel polymer electrolyte (GPE) and an oxygen doped inorganic sulfide solid electrolyte. The O doped sulfide solid electrolyte improves its chemical stability and suppresses the lithium dendrites. A thin GPE film protects the crystal structural stability during cycles and greatly enhances the performance of O doped sulfide solid electrolyte due to the GPE not only constructs soft interface contact between S cathode and solid electrolyte, but also builds lithium ion transport paths by ionic liquid between them. Those SSLSBs display a very good cycling performance with the specific capacity of 1023 mAh/g after 50 cycles at 60 °C and 541 mAh/g after 150 cycles at 30 °C under same rate of 0.1 C. This study demonstrates that the development of advanced solid-state Li-S battery needs to fully integrate a number of technical advantages.
研究领域:
电化学
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材料科学
·
固态电池
·
能源存储
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界面化学
·
纳米材料
·
电极材料
✓ 已验证
DOI
高影响因子
Science China-Materials
·
2021
·Vol. 65
·期 1
·43-50
·
IF 8.273
Xu Jingyi,Lai Chenling,Duan LiPing,Zhang Yuxuan,Xu Yifan,Bao Jianchun,Zhou Xiaosi
Transition-metal compounds have received extensive attention from researchers due to their high reversible capacity and suitable voltage platform as potassium-ion battery anodes. However, these materials commonly feature a poor conductivity and a large volume expansion, thus leading to underdeveloped rate capability and cyclic stability. Herein, we successfully encapsulated ultrafine CoP and CoSb nanoparticles into rich N-doped carbon nanofibers (NCFs) via electrospinning, carbonization, and phosphorization (antimonization). The N-doped carbon fiber prevents the aggregation of nanoparticles, buffers the volume expansion of CoP and CoSb during charging and discharging, and improves the conductivity of the composite material. As a result, the CoP/NCF anode exhibits excellent potassium-ion storage performance, including an outstanding reversible capacity of 335 mA h g −1 , a decent capacity retention of 79.3% after 1000 cycles at 1 A g −1 and a superior rate capability of 148 mA h g −1 at 5 A g −1 , superior to most of the reported transition-metalbased potassium-ion battery anode materials.
研究领域:
材料科学
·
电化学储能
·
纳米材料
·
能源化学
·
功能纤维材料
·
先进电池技术
✓ 已验证
DOI
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2013
·
IF 3.365
Jing Cuan,Bing Yan
In our work, we achieve the multi-component assembly of novel kinds of photofunctional hybrid materials with polyoxometalates (POMs, Na 9 EuW 10 O 36 ·32H 2 O (EuW 10 O 36 9 - denoted as EuW10)) and benzoate (4-aminobenzoate, 4-hydroxybenzoate, 4-mercaptobenzoate) modified mesoporous silica through imidazolium ionic liquid (IL, 1-methyl-3-(trimethoxysilylpropyl) compound as double functional linkage. Using Pluronic P123 surfactant as a template, benzoate functionalized SBA-15 mesoporous host is synthesized as result of the co-condensation of tetraethoxysilane (TEOS) and benzoate modified siloxane as precursor. We fabricate POM into the framework of functionalized SBA-15 mesoporous silica with IL. Here IL behaves as double linkage, which both interact with PMO with electrostatic force through ion exchange and form covalent bond to the functionalized SBA-15 mesoporous silica through its alkoxy group after cohydroxylysis and copolycondensation process. Tb 3+ is further introduced into the above hybrid system through coordination bond to carboxylate group of benzoate unit, which can be expected to modify luminescence color and to obtain close white luminescence. The physical characterizations prove these hybrid materials possess high surface area, uniform mesoporous structure, good crystallization and relatively excellent luminescence properties.
研究领域:
无机化学
·
材料化学
·
纳米功能材料
·
光物理学
·
配位化学
·
溶胶-凝胶科学
·
稀土发光材料
✓ 已验证
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2023
·
IF 7.2
Xingxing Li,Yan Zhu,Nan Zhang,Yansheng Gong,Rui Wang,Huanwen Wang,Jun Jin,Ling Zhao,Beibei He
The development of symmetrical solid oxide fuel cells (SSOFCs) faces a significant challenge in designing electrode materials that exhibit both high activity and stability. In this work, a novel layered perovskite oxide symmetric electrode material PrBaFe 1.8 Hf 0.2 O 5+δ (PBFH) for SSOFCs is proposed and synthesized. Doping Hf at the B-site of PrBaFe 2 O 5+δ (PBF) improves the stability in reducing atmosphere and increases the concentration of oxygen vacancies . Furthermore, a small amount of RuO x is deposited by atomic layer deposition (ALD) onto PrBaFe 1.8 Hf 0.2 O 5+δ scaffold as symmetric electrodes. The surface modification of ALD-RuO x significantly boosts the catalytic activity for both fuel oxidation and oxygen reduction, simultaneously. Compared to PBF electrodes, the interfacial polarization resistances of RuO x -PBFH decrease to 0.77 Ω cm 2 under H 2 /Ar and 0.021 Ω cm 2 under air atmosphere at 800 °C, respectively. At 800 °C, SSOFCs equipped with RuO x -PBFH symmetric electrodes exhibit a high peak power density of 0.85 W cm −2 and 0.41 W cm −2 using humidified hydrogen and propane as fuels, respectively. Moreover, the RuO x -PBFH electrode demonstrates long-lasting performance, displaying high resistance against coking. These findings reveal a facile ALD approach for tailoring symmetric perovskite electrodes, offering robust and efficient electrocatalysis with efficient noble metal utilization.
研究领域:
材料科学
·
电化学
·
能源材料
·
固体离子学
·
催化化学
·
功能陶瓷
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）