CN113797909A - 碳点诱导合成Co9S8/C双功能纳米酶的方法 - Google Patents
碳点诱导合成Co9S8/C双功能纳米酶的方法 Download PDFInfo
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- 229910052799 carbon Inorganic materials 0.000 title claims abstract description 21
- 230000015572 biosynthetic process Effects 0.000 title claims abstract description 10
- 238000003786 synthesis reaction Methods 0.000 title claims abstract description 10
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
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- INPLXZPZQSLHBR-UHFFFAOYSA-N cobalt(2+);sulfide Chemical compound [S-2].[Co+2] INPLXZPZQSLHBR-UHFFFAOYSA-N 0.000 description 1
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Abstract
本发明提供一种碳点诱导合成Co9S8/C双功能纳米酶的方法,该方法将超小的Co9S8纳米颗粒掺入到由CDs拼接形成的多孔二维碳纳米片中。所制备的纳米材料孔结构丰富,具有大的比表面积和出色的双功能纳米酶性能,可以在不施加任何外部能量的情况下模拟过氧化物酶(POD)和氧化酶(OXD)的催化活性,可作为抗坏血酸(AA)的比色传感器,具有较好的抗干扰能力和优异的灵敏度。
Description
技术领域
本发明属于新材料领域,具体涉及一种碳点诱导合成Co9S8/C双功能纳米酶的方法。
背景技术
催化反应的进行需要变价金属离子,如Fe2+/3+,Co2+/3+,Cu1+/2+和Ce3+/4+等,因此,许多含有变价元素的纳米材料表现出模拟酶活性,有望成为天然酶的替代品。天然酶通常制造和储存昂贵,转移不稳定,对恶劣环境敏感。过渡金属Co可形成多种硫化物,如CoS,CoS2,Co2S3,Co3S4和Co9S8等,但其催化活性普遍较低。这主要源于两个方面的原因:首先,它们的纳米粒子不容易赋予小纳米尺寸和均匀分布,限制了活性位点的可及性。其次,与碳基材的弱锚定力使其纳米颗粒不稳定且容易团聚,导致耐久性差。纳米空间限域法在某种程度上克服了上述问题,然而,其制备程序复杂、繁琐、低效且昂贵。
作为一类新的零维(0D)荧光纳米材料,碳点(CDs)因其优秀的电子、光学、物理化学性质以及低成本在如生物医学、化学传感、光催化、电催化,发光二极管,太阳能电池,锂/钠离子电池等领域得到了广泛的应用。从结构上看,CDs由一个羧酸、醇和胺等极性基团组成的壳所包裹的碳核组成。CDs表面的这些杂原子基团从反应性、结合性和氧化还原性质等方面决定了CDs与周围环境的相互作用。例如,通过这些表面基团,CDs可以与大量金属离子(如Fe3+、Ni2+、Cu2+、Ru3+、Co2+)络合,使金属前体稳定的吸附其上。因此,CDs可用作多功能载体或纳米尺寸的模板,以防止在纳米复合材料的制备过程中发生严重的聚集。此外,先前的工作已经证明,CDs可以在高温下拼接成二维(2D)碳纳米片,并导致在其表面形成的产物受到限制。这种策略不仅抑制了新形成的纳米结构的团聚,而且促进了它们在使用中的性能稳定性。
发明内容
为提高钴硫化物的催化活性,克服现有方法复杂、繁琐、低效且昂贵的缺点,提出一种碳点诱导合成Co9S8/C双功能纳米酶的方法,将超小的Co9S8纳米颗粒掺入到由CDs拼接形成的多孔二维碳纳米片中,获得具有大的比表面积、高性能的双功能纳米酶。
为解决上述技术问题,本发明采用的技术方案是:
碳点诱导合成Co9S8/C双功能纳米酶的方法,采用以下步骤:
步骤1将0.075~0.125g CDs粉末加入到15mL无水乙醇或去离子水中,在25℃~35℃、频率20~30KHz环境下超声分散0.5~1h,配制成浓度为5~8.3g/L的碳点溶液;
步骤2将0.075~0.125g氨基磺酸钴溶于15mL体积浓度为25v/v%的氨水溶液中,在25℃~35℃、频率20~30KHz环境下超声分散0.5~1h,配制成浓度为5~8.3g/L的氨基磺酸钴-氨水混合溶液;
步骤3将步骤1得到的碳点溶液在剧烈搅拌下滴加到步骤2得到的氨基磺酸钴-氨水混合溶液中,并持续搅拌0.5~1h,然后将混合溶液放置于电热鼓风干燥箱中,在温度为70~90℃环境下烘干得到固体粉末;
步骤4将步骤3得到的固体粉末研磨0.25~0.5h;
步骤5将由步骤4研磨后的固体粉末放置于管式炉中,以氩气或氮气为保护气体,在温度550~750℃下煅烧2~4h,管式炉升温速率为2~8℃/min,氩气气流量为10~30sccm;然后将管式炉自然冷却到室温,最终得到Co9S8/C双功能纳米酶。
所述CDs粉末依据专利ZL201610534465.4公开的利用煤质沥青制备多色发光可调碳点的方法,采用甲酸与双氧水选择性刻蚀煤沥青获得。
本发明公开碳点诱导合成Co9S8/C双功能纳米酶的方法简便,所制备的纳米材料孔结构丰富,具有大的比表面积和出色的双功能纳米酶性能,可以在不施加任何外部能量的情况下模拟过氧化物酶(POD)和氧化酶(OXD)的催化活性,可作为抗坏血酸(AA)的比色传感器,具有较好的抗干扰能力和优异的灵敏度。
附图说明
图1为本发明制备获得Co9S8/C双功能纳米酶的X射线衍射图谱;
图2为本发明制备获得Co9S8/C双功能纳米酶的透射电镜测试结果;
图3为本发明制备获得Co9S8/C双功能纳米酶的高分辨透射电镜测试结果;
图4为本发明制备获得Co9S8/C双功能纳米酶在添加双氧水(H2O2)的情况下氧化3,3',5,5'-四甲基联苯胺(TMB)底物后溶液的紫外-可见吸收光谱;
图5为本发明制备获得Co9S8/C双功能纳米酶在不添加双氧水(H2O2)的情况下氧化3,3',5,5'-四甲基联苯胺(TMB)底物后溶液的紫外-可见吸收光谱;
图6为Co9S8/C+H2O2+TMB反应体系,固定Co9S8/C和TMB浓度,催化反应速度与双氧水(H2O2)浓度之间的关系;
图7为Co9S8/C+H2O2+TMB反应体系,固定Co9S8/C和H2O2浓度,催化反应速度与TMB浓度之间的关系;
图8为Co9S8/C+TMB反应体系,固定Co9S8/C浓度,催化反应速度与TMB浓度之间的关系;
图9为Co9S8/C+H2O2+TMB反应体系中,加入不同浓度抗坏血酸(AA)后,紫外-可见吸收光谱的叠加图;
图10为Co9S8/C+H2O2+TMB反应体系中,加入不同浓度抗坏血酸(AA)后,反应溶液652nm处吸光度的变化量与AA浓度的关系的线性拟合结果。
具体实施方式
以下结合附图介绍本发明详细技术方案:
碳点诱导合成Co9S8/C双功能纳米酶的方法,采用以下步骤:
步骤1将0.075~0.125g CDs粉末加入到15mL无水乙醇或去离子水中,在25℃~35℃、频率20~30KHz环境下超声分散0.5~1h,配制成浓度为5~8.3g/L的碳点溶液;
步骤2将0.075~0.125g氨基磺酸钴(Co(SO3NH2)2·xH2O)溶于15mL体积浓度为25v/v%的氨水溶液中,在25℃~35℃、频率20~30KHz环境下超声分散0.5~1h,配制成浓度为5~8.3g/L的氨基磺酸钴-氨水混合溶液;
步骤3将步骤1得到的碳点溶液在剧烈搅拌下滴加到步骤2得到的氨基磺酸钴-氨水混合溶液中,并持续搅拌0.5~1h,然后将混合溶液放置于电热鼓风干燥箱中,在温度为70~90℃环境下烘干得到固体粉末;
步骤4将步骤3得到的固体粉末研磨0.25~0.5h;
步骤5将由步骤4研磨后的固体粉末放置于管式炉中,以氩气或氮气为保护气体,在温度550~750℃下煅烧2~4h,管式炉升温速率为2~8℃/min,氩气气流量为10~30sccm;然后将管式炉自然冷却到室温,最终得到Co9S8/C双功能纳米酶。
所述CDs粉末依据专利ZL201610534465.4公开的利用煤质沥青制备多色发光可调碳点的方法,采用甲酸与双氧水选择性刻蚀煤沥青获得。
实施例1
碳点诱导合成Co9S8/C双功能纳米酶的方法,采用以下步骤:
步骤1将0.1g CDs粉末加入到15mL无水乙醇或去离子水中,在35℃、频率30KHz环境下超声分散1h,配制成浓度为6.7g/L的碳点溶液;
步骤2将0.1g氨基磺酸钴溶于15mL体积浓度为25v/v%的氨水溶液中,在35℃、频率30KHz环境下超声分散1h,配制成浓度为6.7g/L的氨基磺酸钴-氨水混合溶液;
步骤3将步骤1得到的碳点溶液在剧烈搅拌下滴加到步骤2得到的氨基磺酸钴-氨水混合溶液中,并持续搅拌1h,然后将混合溶液放置于电热鼓风干燥箱中,在温度为90℃环境下烘干得到固体粉末;
步骤4将步骤3得到的固体粉末研磨0.5h;
步骤5将由步骤4研磨后的固体粉末放置于管式炉中,以氩气或氮气为保护气体,在温度700℃下煅烧4h,管式炉升温速率为5℃/min,氩气气流量为30sccm;然后将管式炉自然冷却到室温,最终得到Co9S8/C双功能纳米酶。
对制备获得的Co9S8/C双功能纳米酶进行表征。本发明制备获得Co9S8/C双功能纳米酶的X射线衍射图谱见图1,图谱显示的衍射峰与Co9S8标准卡片(PDF#75-2023)相一致。
本发明制备获得Co9S8/C双功能纳米酶的透射电镜测试结果见图2,从图中可以看到黑色纳米颗粒均匀分布在浅黑色碳基底上。
本发明制备获得Co9S8/C双功能纳米酶的高分辨透射电镜测试结果如图3所示,图中测得晶粒晶格条纹距离为0.29nm,与Co9S8(311)晶面间距相符,说明黑色颗粒是Co9S8纳米颗粒。
本发明制备获得Co9S8/C双功能纳米酶在添加双氧水(H2O2)的情况下氧化3,3',5,5'-四甲基联苯胺(TMB)底物后溶液的紫外-可见吸收光谱见图4,说明其具有类过氧化物酶活性。
本发明制备获得Co9S8/C双功能纳米酶在不添加双氧水(H2O2)的情况下氧化3,3',5,5'-四甲基联苯胺(TMB)底物后溶液的紫外-可见吸收光谱如图5所示,说明其具有类氧化物酶活性。
本发明制备获得Co9S8/C双功能纳米酶的类过氧化物酶催化反应动力学模型见图6和图7,由图可见,其类过氧化物酶催化反应动力学模型遵循典型Michaelis-Menten动力学模型。
本发明制备获得Co9S8/C双功能纳米酶的类氧化物酶催化反应动力学模型见图8,由图可见,其类氧化物酶催化反应动力学模型也遵循典型Michaelis-Menten动力学模型。
图9和图10说明本发明制备获得Co9S8/C双功能纳米酶可以用作比色检测AA。
Claims (2)
1.碳点诱导合成Co9S8/C双功能纳米酶的方法,其特征在于:采用以下步骤:
步骤1将0.075~0.125g CDs粉末加入到15mL无水乙醇或去离子水中,在25℃~35℃、频率20~30KHz环境下超声分散0.5~1h,配制成浓度为5~8.3g/L的碳点溶液;
步骤2将0.075~0.125g氨基磺酸钴溶于15mL体积浓度为25v/v%的氨水溶液中,在25℃~35℃、频率20~30KHz环境下超声分散0.5~1h,配制成浓度为5~8.3g/L的氨基磺酸钴-氨水混合溶液;
步骤3将步骤1得到的碳点溶液在剧烈搅拌下滴加到步骤2得到的氨基磺酸钴-氨水混合溶液中,并持续搅拌0.5~1h,然后将混合溶液放置于电热鼓风干燥箱中,在温度为70~90℃环境下烘干得到固体粉末;
步骤4将步骤3得到的固体粉末研磨0.25~0.5h;
步骤5将由步骤4研磨后的固体粉末放置于管式炉中,以氩气或氮气为保护气体,在温度550~750℃下煅烧2~4h,管式炉升温速率为2~8℃/min,氩气气流量为10~30sccm;然后将管式炉自然冷却到室温,最终得到Co9S8/C双功能纳米酶。
2.根据权利要求1所述的碳点诱导合成Co9S8/C双功能纳米酶的方法,其特征在于:所述CDs粉末依据专利ZL201610534465.4公开的利用煤质沥青制备多色发光可调碳点的方法,采用甲酸与双氧水选择性刻蚀煤沥青获得。
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