Nie Linchun, Jiang Liushan, Li Shuangying, Song Denghao, Dong Guangyu, Bu Lutong, Chen Chunmao, Zhou Qingxiang
College of Chemical Engineering and Environment, China University of Petroleum-Beijing, Beijing, 102249, China.
College of Chemical Engineering and Environment, China University of Petroleum-Beijing, Beijing, 102249, China.
Talanta. 2024 Aug 1;275:126119. doi: 10.1016/j.talanta.2024.126119. Epub 2024 Apr 16.
Present work reported a novel nanozyme g-CN@Cu, N-CDs with excellent peroxidase-like activity obtained by loading Cu and N co-doped carbon dots on g-CN (graphitic carbon nitride). g-CN@Cu, N-CDs can catalyze HO to generate hydroxyl radical •OH, which oxidizes o-phenylenediamine to 2,3-diaminophenazine, which emits orange fluorescence under ultraviolet light irradiation. The experimental results confirmed that 1,4-benzenedithiol (BDT) could inhibit the peroxidase-like activity of g-CN@Cu, N-CDs. Based the principle above, a colorimetric-fluorescence dual-mode sensor for rapidly sensing of BDT was creatively constructed with assisting of a smartphone. The sensor showed excellent linearity over ranges of 0.75-132 μM and 0.33-60.0 μM with detection limits of 0.32 μM and 0.25 μM for colorimetric and fluorescence detection, respectively. Moreover, a smartphone-assisted colorimetric array sensor was constructed to distinguish six sulfur-containing compounds according to the difference in the degree of inhibition of nanozyme activity by different sulfur-containing compounds. The array sensor could distinguish sulfur-containing compounds at low concentration as low as 0.4 μM. The results validated that the designed sensor was a convenient and fast platform, which could be utilized as a reliably portable tool for the efficient and accurate detection of BDT and the discrimination of multiple sulfur compounds in real water samples.
目前的工作报道了一种新型纳米酶g-CN@Cu,N-CDs,它通过将铜和氮共掺杂的碳点负载在g-CN(石墨相氮化碳)上获得,具有优异的过氧化物酶样活性。g-CN@Cu,N-CDs可以催化H₂O₂生成羟基自由基•OH,后者将邻苯二胺氧化为2,3-二氨基吩嗪,其在紫外光照射下发出橙色荧光。实验结果证实,1,4-苯二硫醇(BDT)可以抑制g-CN@Cu,N-CDs的过氧化物酶样活性。基于上述原理,在智能手机的辅助下,创造性地构建了一种用于快速检测BDT的比色-荧光双模式传感器。该传感器在0.75-132 μM和0.33-60.0 μM范围内表现出优异的线性,比色检测和荧光检测的检测限分别为0.32 μM和0.25 μM。此外,构建了一种智能手机辅助的比色阵列传感器,根据不同含硫化合物对纳米酶活性抑制程度的差异来区分六种含硫化合物。该阵列传感器可以区分低至0.4 μM的低浓度含硫化合物。结果验证了所设计的传感器是一个方便快捷的平台,可作为一种可靠的便携式工具,用于高效准确地检测BDT以及鉴别实际水样中的多种含硫化合物。