检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:尤春琴 罗民[1] 阚夏梅 付蓉蓉[1] 梁斌[1]
机构地区:[1]宁夏大学化学化工学院能源化工重点实验室,银川750021
出 处:《应用化学》2015年第12期1455-1461,共7页Chinese Journal of Applied Chemistry
基 金:国家自然科学基金资助项目(21361020;21561026)~~
摘 要:通过一步水热法分别合成了α-Ni S、Co_3S_4和Co Ni_2S_4纳米介孔电极材料,并研究了其电化学性能。X射线衍射(XRD)、扫描电子显微镜(SEM)和透射电子显微镜(TEM)研究表明,介孔硫化物是由单相纳米颗粒堆叠组装而成,其中二元系的Co Ni_2S_4由纳米片自组装形成了具有皱褶表面的微球形貌。电化学性能研究表明,二元系的Co Ni_2S_4比α-Ni S、C o_3S_4具有更高的比电容、更佳的倍率特性和优异的循环稳定性。在扫描速率为5 m V/s时,Co Ni_2S_4材料在6 mol/L KOH电解液中比电容高达1678.3 F/g,优于α-Ni S(787.4 F/g)和Co_3S_4(1532.7 F/g),在扫描速率从5 m V/s增加到100 m V/s时,其电容保持率为45.8%,比α-Ni S(30.2%)和Co_3S_4(29.3%)高出约15%。在15A/g的电流密度下,经过900次循环充-放电后,二元系的Co Ni_2S_4的电容仍保持在96.3%,库伦效率保持在94.3%左右,说明镍钴双金属硫化物具有优异的循环稳定性能和充放电可逆性。Mesoporous α-NiS, Co3S4 and CoNi2S4 electrode materials were synthesized by a simple one-step hydrothermal method, and their electrochemical properties were investigated. X-ray diffraction and electron microscopy results show that as-obtained mesoporous sulfide electrode materials are assembled by single-phase sulfide nanoparticles and the CoNi2S4 electrode materials have the unique structure of ruffle-like microspheres consisting of 2D nanoplates. The binary CoNi2S4 electrode exhibits much higher specific capacitance of 1678.3 F/g than that of either Co3S4(1532.7 F/g) or α-NiS(787.4 F/g) in 6 mol/L KOH at a scan rate of 5 mV/s, and shows excellent capability retention of 45.8% from 5 mV/s to 100 mV/s, which is ~15% higher than that of α-NiS and Co3S4. The excellent cycling stability of binary CoNi2S4 electrode is achieved with 96.3% of the initial capacitance over 900 consecutive cycles at 15 A/g. Moreover, the columbic efficiency consistently remains above 94.3% within 900 cycles. The fine specific capacitance and good cycling stability demonstrate that the mesoporous CoNi2S4 electrode has potential applications in supercapacitors.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.179