Aflatoxin B1 (AFB1), as the secondary metabolite of molds, is the most predominant and toxic mycotoxin that seriously threatens the health of humans and animals. In this work, an AFB1-responsive hydrogel was synthesized for highly sensitive and portable detection of AFB1. The AFB1-responsive hydrogel was prepared using an AFB1 aptamer and its two short complementary DNA strands as cross-linkers. For visual detection of AFB1, the hydrogel is preloaded with gold nanoparticles (AuNPs). Upon introduction of AFB1, the AFB1 aptamer binds with AFB1, leading to the disruption of the hydrogel and release of the AuNPs with a distinct color change of the supernatant from colorless to red. In order to lower the detection limit and extend the method to quantitative analysis, a distance-readout volumetric bar chart chip (V-chip) was combined with an AFB1-responsive hydrogel preloaded with platinum nanoparticles (PtNPs). In the presence of AFB1, the hydrogel collapses and releases PtNPs which can catalyze the decomposition of H2O2 to generate O2. The increasing gas pressure moves a red ink bar in the V-chip and provides a quantitative relationship between the distance and the concentration of AFB1. The method was applied for detection of AFB1 in beer, with a detection limit of 1.77 nM (0.55 ppb) where an immunoaffinity column (IAC) of AFB1 was used to cleanup and pre-concentrate the sample, which satisfies the testing requirement of 2.0 ppb set by the European Union. The combination of an AFB1-responsive hydrogel with a distance-based readout V-chip offers a user-friendly POCT device, which has great potential for rapid, portable, selective, and quantitative detection of AFB1 in real samples to ensure food safety and avoid subsequent economic losses.

Oxygen electrocatalysis, including both oxygen evolution reaction (OER) and oxygen reduction reaction (ORR), dominates the performance of various electrochemical energy conversion and storage systems. However, the practical applications of these devices are limited as a result of the sluggish kinetics of OER and ORR as well as the high cost and instability of the state-of-the-art noble metal catalyst used in these systems. In this study, cation deficiency is introduced to the A-site of perovskite LaCoO 3 synthesized via polymer-assisted approach to enhance the electrocatalytic activity of both OER and ORR, leading to the boosted bifunctionality of the resultant electrocatalysts, which might be attributed to oxygen vacancy introduction in perovskites. The bifunctionality of the A-site deficiency perovskite (ΔE = 0.948 V) is comparable or even better than the pristine LaCoO 3 (ΔE = 1.063 V) as well as the reported state-of-the-art electrocatalysts, including both perovskites and noble metal electrocatalysts. The stability test also indicates their good stability under alkaline solutions, suggesting that the as-prepared materials can be good candidates as bifunctional electrocatalysts in oxygen-based electrochemical devices, such as fuel cells and metal-air batteries. This work introduces the A-site cation deficiency strategy to improve the bifunctional electrocatalytic performance of perovskites, and highlights the facile polymer-assisted approach for perovskites synthesis.[a] Dr.

Lithium transition-metal oxides (LiMn2O4 and LiMO2 where M = Ni, Mn, Co, etc.) are widely applied as cathode materials in lithium-ion batteries due to their considerable capacity and energy density. However, multiple processes occurring at the cathode/electrolyte interface lead to overall performance degradation. One key failure mechanism is the dissolution of transition metals from the cathode. This work presents results combining scanning electrochemical microscopy with inductively coupled plasma (ICP) and electron paramagnetic resonance (EPR) spectroscopies to examine cathode degradation products. Our effort employs a LiMn2O4 (LMO) thin film as a model cathode to monitor the Mn dissolution process without the potential complications of conductive additive and polymer binders. We characterize the electrochemical behavior of LMO degradation products in various electrolytes, paired with ICP and EPR, to better understand the properties of Mn complexes formed following metal dissolution. We find that the identity of the lithium salt anions in our electrolyte systems [ClO4 –, PF6 –, and (CF3SO2)2N–] appears to affect the Mn dissolution process significantly as well as the electrochemical behavior of the generated Mn complexes. This implies that the mechanism for Mn dissolution is at least partially dependent on the lithium salt anion.

Traditional immunochromatographic test strips based on colloidal gold are effective devices for portable and low-cost point-of-care (POC) testing. Nevertheless, they still suffer from the limitation of qualitative or semiquantitative tests via naked-eye detection. Replacement of gold with other signal entities, such as magnetic particles or fluorescent particles, requires professional instrumentation to obtain quantitative results. A pressure-based assay with platinum nanoparticles (PtNPs) can provide quantitative results using a portable pressure meter but is also hampered by the long-term instability of PtNPs. Consequently, we developed a Pt-staining method based on test strips to create platinum nanoshells on the surface of colloidal gold. This method not only preserves the original advantages of colloidal gold with easy synthesis and decoration but also introduces PtNPs with excellent catalytic activity as signal labels to achieve sensitive quantitative detection. Myoglobin was tested as a model target, and the limit of detection was 5.47 ng/mL in 20% diluted serum samples, which satisfies the requirements for clinical monitoring of acute myocardial infarction. In addition, the two most common colloidal gold strips available in the marketplace were applied to demonstrate the compatibility of Pt-staining. Taking advantage of low cost, user-friendliness, compatibility, simplicity, and stability, colloidal gold test strips with Pt-staining are expected to satisfy the need for quantitative POC testing of biomarkers, especially in resource-limited regions.

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LiNi0.5Co0.2Mn0.3O2 (NCM523), as a cathode material for rechargeable lithium-ion batteries, has attracted considerable attention and been successfully commercialized for decades. NCM is also a promising electrocatalyst for the oxygen evolution reaction (OER), and the catalytic activity is highly correlated to its structure. In this paper, we successfully obtain NCM523 with three different structures: spinel NCM synthesized at low temperature (LT-NCM), disordered NCM (DO-NCM) with lithium deficiency obtained at high temperature, and layered hexagonal NCM at high temperature (HT-NCM). By introducing lithium deficiency to tune the valence state of transition metals in NCM from Ni2+ to Ni3+, DO-NCM exhibits the best catalytic activity with the lowest onset potential (∼1.48 V) and Tafel slope (∼85.6 mV dec–1), whereas HT-NCM exhibits the worst catalytic activity with the highest onset potential (∼1.63 V) and Tafel slope (∼241.8 mV dec–1).

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