CN107685153A - 一种贵金属纳米复合结构的构筑 - Google Patents
一种贵金属纳米复合结构的构筑 Download PDFInfo
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Abstract
本发明涉及一种贵金属纳米复合结构的构筑,包括:将50‑70ml去离子水于64.8ul的0.04‑0.06g/mlHAuCl4混合,搅拌并加热至沸腾,然后加入3ml2%的柠檬酸钠,继续沸腾10‑30分钟后,冷却至室温,即得到金纳米粒子;从其中取出10.7ml并加入600ul的40mM的十二烷基硫酸钠和600ul的10mM的吡咯,进行剧烈搅拌,然后加入3ml的2mM的过二硫酸铵,室温下搅拌24‑48h,然后在6500r的转速下离心10‑30min,最后得到聚吡咯涂层的贵金属纳米复合结构。
Description
技术领域
本发明涉及一种贵金属纳米复合结构的构筑,属于合成化学领域。
背景技术
贵金属纳米材料具有优异的物理特性和化学特性,例如量子尺寸效应、表面效应、小尺寸效应以及宏观量子效应,并且在光、力、磁、电、表面催化和生物传感器等领域都有着举足轻重的作用,可以作为电极材料、仿生类材料、磁性存储类材料以及各类敏感材料等方面,都有着十分广泛的应用前景。但是贵金属纳米材料的物理性质和化学性质会受到其自身的尺寸和形貌等因素的影响。所以该领域的研究者一般都可以在合成这类金属纳米材料的过程中,然后通过调整上述的各种物理参数,进而依据人们的意愿制备出具有特定功能的贵金属纳米材料。就目前来看,研究中所发现的具有特定形貌的纳米晶体,他自身暴露在外面的晶面一般是特定的,因此这些特定的晶面所包含的原子的各种堆积方式以及数目也有差别,所以表现出来的性质也各不相同。对于贵金属纳米晶体材料来说,形貌的规则性不仅关系到外观,更重要的是对其自身性质的作用。但是,如今有关贵金属纳米材料合成还是没有实现较好的可控性,而且对于晶体的成核过程以及生长过程的机理探索的也不是十分清楚。
发明内容
本发明所要解决的技术问题是提供一种贵金属纳米复合结构的构筑,技术方案如下:将50-70ml去离子水于64.8ul的0.04-0.06g/mlHAuCl4混合,搅拌并加热至沸腾,然后加入3ml2%的柠檬酸钠,继续沸腾10-30分钟后,冷却至室温,即得到金纳米粒子;从其中取出10.7ml并加入600ul的40mM的十二烷基硫酸钠和600ul的10mM的吡咯,进行剧烈搅拌,然后加入3ml的2mM的过二硫酸铵,室温下搅拌24-48h,然后在6500r的转速下离心10-30min,最后得到聚吡咯涂层的贵金属纳米复合结构。
本发明的有益效果是:制备工艺简易环保,成本低,适用范围广。
具体实施方式
实施例1
将50ml去离子水于64.8ul的0.04g/mlHAuCl4混合,搅拌并加热至沸腾,然后加入3ml2%的柠檬酸钠,继续沸腾10分钟后,冷却至室温,即得到金纳米粒子;从其中取出10.7ml并加入600ul的40mM的十二烷基硫酸钠和600ul的10mM的吡咯,进行剧烈搅拌,然后加入3ml的2mM的过二硫酸铵,室温下搅拌24h,然后在6500r的转速下离心10min,最后得到聚吡咯涂层的贵金属纳米复合结构。
实施例2
将70ml去离子水于64.8ul的0.06g/mlHAuCl4混合,搅拌并加热至沸腾,然后加入3ml2%的柠檬酸钠,继续沸腾30分钟后,冷却至室温,即得到金纳米粒子;从其中取出10.7ml并加入600ul的40mM的十二烷基硫酸钠和600ul的10mM的吡咯,进行剧烈搅拌,然后加入3ml的2mM的过二硫酸铵,室温下搅拌48h,然后在6500r的转速下离心30min,最后得到聚吡咯涂层的贵金属纳米复合结构。
实施例3
将60ml去离子水于64.8ul的0.05g/mlHAuCl4混合,搅拌并加热至沸腾,然后加入3ml2%的柠檬酸钠,继续沸腾20分钟后,冷却至室温,即得到金纳米粒子;从其中取出10.7ml并加入600ul的40mM的十二烷基硫酸钠和600ul的10mM的吡咯,进行剧烈搅拌,然后加入3ml的2mM的过二硫酸铵,室温下搅拌36h,然后在6500r的转速下离心20min,最后得到聚吡咯涂层的贵金属纳米复合结构。
以上所述仅为本发明的较佳实施例,并不用以限制本发明,凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (2)
1.一种贵金属纳米复合结构的构筑,其特征在于,包括:将50-70ml去离子水于64.8ul的0.04-0.06g/mlHAuCl4混合,搅拌并加热至沸腾,然后加入3ml2%的柠檬酸钠,继续沸腾10-30分钟后,冷却至室温,即得到金纳米粒子;从其中取出10.7ml并加入600ul的40mM的十二烷基硫酸钠和600ul的10mM的吡咯,进行剧烈搅拌,然后加入3ml的2mM的过二硫酸铵,室温下搅拌24-48h,然后在6500r的转速下离心10-30min,最后得到聚吡咯涂层的贵金属纳米复合结构。
2.根据权利要求1所述的合成方法,其特征在于,所述反应温度为90-100度。
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Citations (5)
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CN101306468A (zh) * | 2007-05-19 | 2008-11-19 | 浙江师范大学 | 导电聚吡咯包裹铜银复合纳米粒子的制备方法 |
CN102321344A (zh) * | 2011-09-21 | 2012-01-18 | 中国科学院理化技术研究所 | 聚(3,4-二氧乙基)噻吩与金纳米粒子复合材料的制备方法 |
CN104130405A (zh) * | 2014-05-16 | 2014-11-05 | 盐城工学院 | 一种钴/聚吡咯纳米复合吸波材料及其制备方法 |
CN104280441A (zh) * | 2014-10-15 | 2015-01-14 | 甘肃省科学院传感技术研究所 | 一种Au@Ag-PPY复合纳米材料和L-半胱氨酸双层膜固定葡萄糖氧化酶修饰电极的制备方法 |
CN106958017A (zh) * | 2010-12-07 | 2017-07-18 | 罗地亚管理公司 | 包括纳米结构体的导电聚合物膜、制备聚合物膜的方法以及包括该膜的电子装置 |
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- 2017-09-06 CN CN201710796594.5A patent/CN107685153A/zh not_active Withdrawn
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101306468A (zh) * | 2007-05-19 | 2008-11-19 | 浙江师范大学 | 导电聚吡咯包裹铜银复合纳米粒子的制备方法 |
CN106958017A (zh) * | 2010-12-07 | 2017-07-18 | 罗地亚管理公司 | 包括纳米结构体的导电聚合物膜、制备聚合物膜的方法以及包括该膜的电子装置 |
CN102321344A (zh) * | 2011-09-21 | 2012-01-18 | 中国科学院理化技术研究所 | 聚(3,4-二氧乙基)噻吩与金纳米粒子复合材料的制备方法 |
CN104130405A (zh) * | 2014-05-16 | 2014-11-05 | 盐城工学院 | 一种钴/聚吡咯纳米复合吸波材料及其制备方法 |
CN104280441A (zh) * | 2014-10-15 | 2015-01-14 | 甘肃省科学院传感技术研究所 | 一种Au@Ag-PPY复合纳米材料和L-半胱氨酸双层膜固定葡萄糖氧化酶修饰电极的制备方法 |
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