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Dawson-type polyoxometalate nanoclusters confined in a carbon nanotube matrix as efficient redox mediators for enzymatic glucose biofuel cell anodes and glucose biosensors
Biosensors and Bioelectronics ( IF 12.6 ) Pub Date : 2018-02-28 , DOI: 10.1016/j.bios.2018.02.060
Feriel Boussema , Andrew J. Gross , Fatma Hmida , Brahim Ayed , Hatem Majdoub , Serge Cosnier , Abderrazak Maaref , Michael Holzinger

Two new inorganic-organic hybrid materials based on heteropolyoxometalates (POMs): (C4H10N)6[P2Mo18O62]·4H2O (P2Mo18) and (C6H8NO)4[H2P2W18O62]·6H2O (P2W18) are reported as mediators for electron transfer between FAD-dependent glucose dehydrogenase (FAD-GDH) and a multiwalled carbon nanotube (MWCNT) matrix for glucose biofuel cell and biosensor applications. These polyoxometalates were chosen due to their promising redox behavior in a potential range for mediated electron transfer with the glucose oxidizing enzyme, FAD-GDH. P2Mo18 and P2W18 were immobilized on 1-pyrenemethylamine (PMA) functionalized MWCNT deposits. After immobilization of FAD-GDH, the P2W18-modified MWCNT electrode demonstrated mediated electron transfer and provided a catalytic current density of 0.34 mA cm−2 at 0.2 V vs SCE with an open circuit potential (OCP) of −0.08 V vs SCE. A 10-fold increase in catalytic current to 4.7 mA cm−2 at 0.2 V vs SCE and a slightly lower OCP of −0.10 V vs SCE was observed for an equivalent electrode modified with P2Mo18.The apparent superiority of P2Mo18 is related, at least in part, to its improved incorporation in the MWCNT matrix compared to P2W18. Both POM-modified bioanodes showed exceptional stabilities with 45% of their initial performances remaining after 15 days. The mediated electron transfer capacities of the POMs were also evaluated in a glucose sensor setup and showed very satisfying performances for glucose detection, including a sensitivity of 0.198 mA mol L−1 cm−2, a satisfying linear range between 1 mmol L−1 and 20 mmol L−1, and good reproducibility for the P2Mo18 electrode.



中文翻译:

Dawson型多金属氧酸盐纳米簇被限制在碳纳米管基质中,作为酶促葡萄糖生物燃料电池阳极和葡萄糖生物传感器的有效氧化还原介体。

基于杂多金属氧酸盐(POM)的两种新型无机-有机杂化材料:(C 4 H 10 N)6 [P 2 Mo 18 O 62 ]·4H 2 O(P 2 Mo 18)和(C 6 H 8 NO)4 [ H 2 P 2 W 18 O 62 ]·6H 2 O(P 2 W 18)被报道为FAD依赖性葡萄糖脱氢酶(FAD-GDH)和用于葡萄糖生物燃料电池和生物传感器应用的多壁碳纳米管(MWCNT)基质之间电子转移的介体。选择这些多金属氧酸盐是因为它们在氧化葡萄糖酶FAD-GDH介导的电子转移的潜在范围内具有良好的氧化还原行为。将P 2 Mo 18和P 2 W 18固定在1-py甲基胺(PMA)功能化的MWCNT沉积物上。固定FAD-GDH后,P 2 W 18修饰的MWCNT电极表现出介导的电子转移,并提供0.34 mA cm -2的催化电流密度在0.2 V vs SCE的情况下,开路电势(OCP)在-0.08 V vs SCE的情况下。在催化电流4.7毫安厘米有10倍增加-2观察到的P改性的等效电极以0.2V相对于SCE和-0.10的V相对于SCE稍低OCP 218 P的.The表观优越性2图18至少部分地涉及与P 2 W 18相比其在MWCNT基体中的改进的结合。。两种POM修饰的生物阳极均表现出出色的稳定性,在15天后仍保留其初始性能的45%。还通过葡萄糖传感器设置评估了POM的介导电子转移能力,并显示出非常令人满意的葡萄糖检测性能,包括0.198 mA mol L -1 cm -2的灵敏度,1 mmol L -1和1 mmol L的令人满意的线性范围。20 mmol L -1,对于P 2 Mo 18电极具有良好的重现性。

更新日期:2018-02-28
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