Nitrite is commonly found in various aspects of daily life, but its excessive intake poses health risks like blood oxygen transport impairment and cancer risks. Accurate detection of nitrite is crucial for preventing its potential harm and ensuring public health. In this work, Cu–Co bimetallic nanoparticles (NPs) incorporated nitrogen-doped carbon dodecahedron (Cu/ Co@N–C/CNTs-X, where X denotes the carbonization temperatures) are synthesized by facile carbonization of CuO@ZIF- 67 composites. Cu and Co NPs are uniformly embedded in the carbon dodecahedron decorated by carbon nanotubes (CNTs) without agglomeration. Combining the superior catalytic from Cu and Co NPs with the electrical conductivity and stability from the carbon frameworks, the Cu/Co@N–C/CNTs-600 composite as catalyst detected nitrite concentrations ranging from 1 to 5000 μM, with sensitivity values of 0.708 μA μM–1 cm– 2, and a detection limit of 0.5 μM. Moreover, this sensor demonstrated notable selectivity, stability and reproducibility. The design of Cu/Co@N–C/CNTs-X catalysts prepared in this study can be used as an attractive alternative in the fields of food quality and environmental detection.

다결정성 ZIF-8 분리막의 C3H6/C3H8 kinetic 분리 성능 향상을 목적으로 상대적으로 부피가 큰 2, 4-dimethylimidazole (dmIm)이 ZIF-8 구조 내 2-methylimidazole들을 일부 대체한 혼합 리간드 ZIF-8 유사체 분리막을 이차성장법을 이용 하여 제조하였다. 25°C, 1 bar의 feed 압력에서 C3H6/C3H8 (50/50, V/V) 혼합가스를 대상으로 측정된 분리막의 선택도는 ~180이었으며, 이는 기 보고된 대부분의 다결정성 ZIF-8 분리막들의 선택도보다 높았다. 선택도 향상의 원인인 ZIF-8 구조 내 dmIm 도입으로 인한 기공 입구 크기의 축소를 77 K에서의 질소 등온흡착실험과 Maxwell-Stefan model을 이용하여 C3H6 와 C3H8 막투과도 데이터로부터 계산된 확산계수들을 통해 증명하였다.

Food contamination with heavy-metal ions and nitrites poses a serious threat to human health. Consequently, the development of fast and sensitive platforms for detecting these contaminants is urgently needed. In this study, a novel sensing platform was developed by integrating carbon nanotubes generated by the pyrolysis of waste masks (WMCNTs) with ZIF-8 for the simultaneous detection of Cd2+, Pb2+, and nitrite. Specifically, the electronic structure of the WMCNT backbone was modulated by doping with B and N atoms. Nanoporous ZIF-8 was then grown in-situ on its surface to produce composites with enhanced electrical conductivities and large specific surface areas. This modification provided more active sites for the attachment of heavy-metal ions and nitrites. Under optimized conditions, the sensing platform exhibited a wide linear range with the Pb2+, Cd2+, and NO2 − limits of detection of 2.68, 12.12, and 5.94 μM, respectively. Notably, the sensing platform demonstrated excellent anti-interference capabilities and effectively detected nitrites and heavy-metal ions in pickled foods.

Electrochemical oxidation and reduction reactions are fundamental in various conversion and energy storage devices. Functional materials derived from MOFs have been considered promising as electrical catalysts for ORR, HER, and OER, which can be used in Zinc-air batteries and water electrolysis. Herein, we designed a novel approach to fabricating the ultrafine Co9S8 embedded nitrogen-doped hollow carbon nanocages ( Co9S8@N-HC). The method involved a process of sulfidation of cobalt-based metal–organic frameworks (ZIF67) and then coating them with polypyrrole (PPy). PPy has notable properties such as high electrical conductivity and abundant nitrogen content, rendering it highly promising for catalytic applications. The Co9S8@ N-HC catalyst was successfully synthesized via the carbonization of CoSx@ PPy. Remarkably, the Co9S8@ N-HC catalyst demonstrated exceptional electrocatalytic activity, requiring only low overpotentials of 285 mV and 201 mV at 10 mA cm‒ 2 for OER and HER, respectively, and exhibited high activity for ORR, with an onset potential ( Eonset) of 0.923 V and half-wave potential ( E1/2) of 0.879 V in alkaline media. The electrocatalytic efficiency displayed by Co9S8@ N-HC opens a new line of research on the synergistic effect of MOF-PPy materials on energy storage and conversion.

Herein, facile room-temperature self-assembly and high-temperature pyrolysis strategy was successively conducted for in situ synthesizing novel TiO2/ TiN@N-C heterostructure by using typical sandwich-like precursors (MXene/ZIF-8). Zerodimensional (0D) TiO2, TiN and N-doped carbon nanoparticles were in situ formed and randomly anchored on the twodimensional (2D) N-doped carbon substrate surface, making TiO2/ TiN@N-C exhibit unique 0D/2D heterostructure. Relative to the extensively studied ZIF-8-derived N-doped carbon nanoparticles, TiO2/ TiN@N-C heterostructure displayed greatly boosted electrochemical active specific surface. Benefiting from the enhanced electrochemical property of TiO2/ TiN@N-C heterostructure, remarkable signal enhancement effect was achieved in terms of the oxidation of multiple hazardous substances, including clozapine, sunset yellow and benomyl. As a result, a novel electrochemical platform was constructed, the linear detection range were 10–1000 nM, 2.5–1250 nM, 10–1000 nM while the detection limits were evaluated to be 3.5 nM, 1.2 nM, 4.5 nM for clozapine, sunset yellow and benomyl, respectively. Besides, the practicability of the newly developed electrochemical method was verified by assessing the content of clozapine, sunset yellow and benomyl in real food samples.