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复合氧化物La_(0.6)Ca_(0.4)CoO_3的合成及对氧还原的电催化活性 被引量:1
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作者 马全宝 张正富 +3 位作者 陈红宇 欧阳鹏 徐明丽 陈庆华 《昆明理工大学学报(理工版)》 2005年第3期23-27,共5页
采用溶胶凝胶法,结合高温焙烧和微波焙烧分别合成了La0.6Ca0.4CoO3复合氧化物.凝胶的DSC和TGA分析表明:复合氧化物粉体在680℃左右相转变基本完成.然后以此为依据,对200℃凝胶焙烧的粉体作了X-ray相分析,表明粉体以金属氧化物和金属单... 采用溶胶凝胶法,结合高温焙烧和微波焙烧分别合成了La0.6Ca0.4CoO3复合氧化物.凝胶的DSC和TGA分析表明:复合氧化物粉体在680℃左右相转变基本完成.然后以此为依据,对200℃凝胶焙烧的粉体作了X-ray相分析,表明粉体以金属氧化物和金属单质的形式存在,没有钙钛矿相形成;对700℃、800℃和900℃高温炉焙烧粉体分别做了X-ray相详细分析,结果表明焙烧温度越高,结晶程度越好.又对比了三组微波焙烧所得的粉体和800℃高温炉焙烧粉体的X-ray相,微波焙烧所得粉体也为钙钛矿结构,但与高温焙烧所得粉体相比,结晶程度还不够完整.线性扫描伏安测试表明,用溶胶凝胶法制备的La0.6Ca0.4CoO3电极,在碱性溶液中具有良好的氧还原活性.并且,通过合适的微波焙烧工艺合成的粉体的电催化活性要比高温焙烧所得粉体的催化活性高. 展开更多
关键词 la0.6ca0.4CoO3电极 电催化 溶胶凝胶法
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基于La_(0.6)Ca_(0.4)Fe_(0.7)Sc_(0.1)Ni_(0.2)O_(3-δ)氧电极的可逆固体氧化物电池性能研究
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作者 田云峰 杨偲晨 +7 位作者 李宜桐 章梦云 顾水丹 郑克晴 王鑫鑫 凌意瀚 蒲健 池波 《燃料化学学报》 EI CAS CSCD 北大核心 2022年第12期1638-1646,共9页
本研究制备了10%Sc掺杂的La_(0.6)Ca_(0.4)Fe_(0.7)Sc_(0.1)Ni_(0.2)O_(3−δ)(LCFSN)材料,采用半电池研究了该材料的氧还原催化活性(ORR)和氧析出催化活性(OER),发现LCFSN的ORR催化活性优于OER催化活性。组装了Ni-YSZ((Y_(2)O_(3))_(0.0... 本研究制备了10%Sc掺杂的La_(0.6)Ca_(0.4)Fe_(0.7)Sc_(0.1)Ni_(0.2)O_(3−δ)(LCFSN)材料,采用半电池研究了该材料的氧还原催化活性(ORR)和氧析出催化活性(OER),发现LCFSN的ORR催化活性优于OER催化活性。组装了Ni-YSZ((Y_(2)O_(3))_(0.08)(ZrO_(2))_(0.92))/YSZ/GDC(Gd_(0.1)Ce_(0.9)O_(2−δ))/LCFSN全电池并研究了其在燃料电池模式(SOFC)和电解池模式(SOEC)下的电化学性能,电池在800℃以H_(2)为燃料时的最高功率密度可达1.471 W/cm^(2),在750℃,50%H_(2)O和1.3 V热中性电解电压条件下其产氢速率高达627 mL/(cm^(2)·h)。而且电池在100 h的稳定性测试中性能没有衰减,具有良好的稳定性。通过研究,证明了LCFSN是一个具有良好发展前景的氧电极材料。 展开更多
关键词 可逆固体氧化物电池 氧电极 la_(0.6)ca_(0.4)Fe_(0.7)Sc_(0.1)Ni_(0.2)O_(3−δ) 电化学性能 稳定性
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高性能SOFC薄膜氧电极La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)-Gd_(0.1)Ce_(0.9)O_(1.95)的制备及性能评估
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作者 王章苇 罗凌虹 +5 位作者 程亮 王乐莹 徐序 余剑锋 刘邵帅 张双双 《陶瓷学报》 CAS 北大核心 2023年第4期751-760,共10页
使用对称氧电极电池研究了La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)-Gd_(0.1)Ce_(0.9)O_(1.95)氧电极厚度与其电化学性能间的依赖关系。使用电化学阻抗谱测试方法在开路电压条件下测试了厚度为5μm~22μm的氧电极的电化学阻抗谱。同... 使用对称氧电极电池研究了La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)-Gd_(0.1)Ce_(0.9)O_(1.95)氧电极厚度与其电化学性能间的依赖关系。使用电化学阻抗谱测试方法在开路电压条件下测试了厚度为5μm~22μm的氧电极的电化学阻抗谱。同样制备并测试了不同厚度氧电极的燃料极支撑纽扣电池的电化学阻抗谱和循环伏安曲线。结果表明,随着氧电极厚度的变化,总极化阻抗Rp也随之变化。总极化阻抗来源于氧离子传输、氧表面交换和氧气的扩散过程;解析不同过程的阻抗可以发现,高频的氧离子传输过程与氧电极厚度的依赖性较弱;而氧表面交换过程和氧气的扩散过程与氧电极的依赖性强。通过优化氧电极的厚度能够优化氧电极的电化学性能;当氧电极为12μm时,其阻抗值达到最小值;750℃为0.034Ω·cm^(2。)基于此,在800℃、燃料气为3vol.%H_(2)O+97vol.%H2条件下,燃料极支撑纽扣电池(NiO-YSZ||YSZ||20GDC||LSCF-10GDC)的最大功率密度达到1098 mW·cm^(-2)。由于所获得电池氧电极的最优厚度仅为目前同类电池氧电极厚度的约一半,提出可商业化电池的“高性能薄膜氧电极”概念。 展开更多
关键词 SOFC la_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)-Gd_(0.1)Ce_(0.9)O_(1.95) 氧电极厚度 电化学性能
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Tungsten doping La_(0.6)Ca_(0.4)Fe_(0.8)Ni_(0.2)O_(3-δ)as electrode for highly efficient and stable symmetric solid oxide cells 被引量:1
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作者 Xin-Yi Jiao Ao-Yan Geng +4 位作者 Yi-Yang Xue Xing-Bao Wang Fang-Jun Jin Yi-Han Ling Yun-Feng Tian 《Tungsten》 EI CSCD 2023年第4期598-606,共9页
Perovskite oxide La_(0.6)Ca_(0.4)Fe_(0.8)Ni_(0.2)O_(3-δ)(LCFN)has been used in symmetric solid oxide cells(SSOCs)to obtain good electrochemical performance in both fuel cells(SOFCs)and electrolysis cells(SOECs)modes.... Perovskite oxide La_(0.6)Ca_(0.4)Fe_(0.8)Ni_(0.2)O_(3-δ)(LCFN)has been used in symmetric solid oxide cells(SSOCs)to obtain good electrochemical performance in both fuel cells(SOFCs)and electrolysis cells(SOECs)modes.However,its structural stability still faces challenges and the electrocatalytic activity also needs to be further improved.Herein,tungsten-doped La_(0.6)Ca_(0.4)Fe_(0.7)Ni_(0.2)W_(0.1)0_(3-δ)(LCFNW)perovskite oxide material was synthesized which exhibits good structural stability under H_(2)and superior electrochemical performance as an electrode for SSOCs.In SOFCs mode,the cell achieved the maximum power density of 0.58 W·cm^(-2)with wet H_(2)as fuel at 850℃.In SOECs mode,the current density can reach 1.81 A·cm^(-2)for pure CO_(2)electrolysis at 2 V.Moreover,the SSOCs exhibits outstanding long-term stability in both SOFCs and SOECs modes,proving that doping W in perovskite oxide is an effective strategy to enhance the catalytic activity and stability of the electrode.The LCFNW material developed in this work shows promising prospect as an electrode candidate for SSOCs. 展开更多
关键词 Symmetric solid oxide cells Perovskite oxide la_(0.6)ca_(0.4)Fe_(0.8)Ni_(0.2)O_(3-δ) CO_(2)electrolysis Stability
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Pd-La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)composite as active and stable oxygen electrode for reversible solid oxide cells 被引量:2
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作者 Rui Yang Yunfeng Tian +2 位作者 Yun Liu Jian Pu Bo Chi 《Journal of Rare Earths》 SCIE EI CAS CSCD 2023年第4期599-604,共6页
To promote the electrocatalytic activity and stability of traditional(a_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)(LSCF)oxygen electrodes in reversible solid oxide cells(RSOCs),conventional physical mixed method was used t... To promote the electrocatalytic activity and stability of traditional(a_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)(LSCF)oxygen electrodes in reversible solid oxide cells(RSOCs),conventional physical mixed method was used to prepare the Pd-LSCF composite oxygen electrode.The cell with Pd-LSCF|GDC|YSZ|Ni-YSZ configuration shows perfect electrochemical performance in both solid oxide fuel cell(SOFC)mode and solid oxide electrolysis cell(SOEC)mode.In the SOFC mode,the cell achieves a power density of 1.73 W/cm^(2)at800℃higher than that of the LSCF oxygen electrode with 1.38 W/cm^(2).In the SOEC mode,the current density at 1.5 V is 1.67 A/cm^(2)at 800℃under 50 vol%steam concentration.Moreover,the reversibility and stability of the RSOCs were tested during 192 h long-term reversible operation.The degradation rate of the cell is only 2.2%/100 h and 2.5%/100 h in the SOEC and the SOFC modes,respectively.These results confirm that compositing Pd with the LSCF oxygen electrode can considerably boost the electrochemical performance of LSCF electrode in RSOCs field. 展开更多
关键词 Reversible solid oxide cells COMPOSITE Oxygen electrode la_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ) Electrochemical performance Rare earths
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