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作 者:成巍[1] 陈彩玲[1] 于影[1] 李春光[1] 高路[1] 施展[1]
机构地区:[1]吉林大学无机合成与制备化学国家重点实验室,化学学院,长春130012
出 处:《高等学校化学学报》2017年第8期1303-1308,共6页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:21371069)资助~~
摘 要:通过两步法设计合成了具有中空结构的双金属硫化物(Zn,Co)S纳米晶,并研究了其电化学性质.首先在室温下,以水为溶剂,十六烷基三甲基溴化铵为表面活性剂,利用Zn^(2+),Co^(2+)与2-甲基咪唑的配位作用形成了ZIF-Zn,Co.然后以ZIF-Zn,Co为自牺牲模板剂,加入硫代乙酰胺,在微波辐射下快速合成了具有中空结构的(Zn,Co)S纳米晶.电化学测试结果表明,在电流密度为3 mA/cm^2时,(Zn,Co)S纳米晶比电容为423.3 F/g,在电流密度为10 mA/cm^2时,充放电2000次,仍能保持59%的初始电容.所制备的中空纳米结构具有较高的比表面积和较好的电化学性能,可作为超级电容器的电极材料.A simple two-step method was introduced to synthesize uniform and hollow (Zn, Co)S nanostructures. Firstly, the bimetal compound ZIF-Zn, Co(ZIF = zeolitic imidazolate frameworks) with metal ions( gn^2+ and Co^2+) and ligand(2-methylimidazole) was obtained using deionized water as solvent, hexadeeyhrimethyl- ammonium bromide (CTAB) as capping agent under stirring at room temperature. Secondy, hollow (Zn, Co)S nanostructures were synthesized by selecting ZIF-Zn, Co as self-saerificial template and adding thioacetamide (TAA) as sulfate source under the mierowave-assisted heating condition. The electrochemical measurements show that the speeific capaeitanee of the as-made hollow (Zn, Co)S nanostructures was 423.3 F/g at current density of 3 mA/cm^2 and 57% capacitanee remains after 2000 cycles at a current density of 10 mA/cm^2. With the advantages of unique properties, such as high surface area and good eleetrochemical performance, the as-made hollow (Zn, Co)S nanostruetures have great potential as eleetrode material for supereapaeitors.
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