Driven Kerr nonlinear optical resonators can sustain localized structures known as dissipative Kerr cavity solitons, which have recently attracted significant attention as the temporal counterparts of microresonator optical frequency combs. While conventional wisdom asserts that bright cavity solitons can only exist when driving in the region of anomalous dispersion, recent theoretical studies have predicted that higher-order dispersion can fundamentally alter the situation, enabling bright localized structures even under conditions of normal dispersion driving. Here we demonstrate a flexible optical fiber ring resonator platform that offers unprecedented control over dispersion conditions, and we report on the first experimental observations of bright localized structures that are fundamentally enabled by higher-order dispersion. In broad agreement with past theoretical predictions, we find that several distinct bright structures can coexist for the same parameters, and we observe experimental evidence of their collapsed snaking bifurcation structure. Our results also elucidate the physical mechanisms that underpin the bright structures, highlighting the key role of spectral recoil due to dispersive wave emission. In addition to enabling direct experimental verifications of a number of theoretical predictions, we show that the ability to judiciously control the dispersion conditions offers a novel route for ultrashort pulse generation: the bright structures circulating in our resonator correspond to pulses of light as short as 230 fs—the record for a passive all-fiber ring resonator. We envisage that our work will stimulate further fundamental studies on the impact of higher-order dispersion on Kerr cavity dynamics, as well as guide the development of novel ultrashort pulse sources and dispersion-engineered microresonator frequency combs.
Excessive antibiotic residues in food can cause detrimental effects on human health. The establishment of rapid, sensitive, selective, and reliable methods for the detection of antibiotics is highly in demand. With the inherent advantages of high sensitivity, rapid analysis time, and facile miniaturization, the electrochemical sensors have great potential in the detection of antibiotics. The electrochemical platforms comprising carbon nanomaterials (CNMs) have been proposed to detect antibiotic residues. Notably, with the introduction of functional CNMs, the performance of electrochemical sensors can be bolstered. This review first presents the significance of functional CNMs in the detection of antibiotics. Subsequently, we provide an overview of the applications for detection by enhancing the electrochemical behaviour of the antibiotic, as well as a brief overview of the application of recognition elements to detect antibiotics. Finally, the trend and the current challenges of electrochemical sensors based on CNMs in the detection of antibiotics is outlined.
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