Search arXivSearch

arXiv · 2511.04493

A copper sulfide-hydroxypropyl $β$-Cyclodextrin-reduced graphene oxide composite for highly sensitive electrochemical detection of 5-hydroxytryptamine in biological samples

Abstract

The precise identification of neurotransmitters is essential for comprehending cerebral function, detecting neurological conditions, and formulating successful therapeutic approaches. The present work investigates the electrochemical detection of serotonin with the excellent hybrid electrocatalyst $Cu_2S/Hβcd-rGO$. $Cu_2S$, with its significant features as improved catalytic activity and enhanced charge transfer when combined with $Hβcd-rGO$, will enhance the performance. The integration of $Cu_2S$ with $Hβcd-rGO$, regulated by the van der Waals force and the electrostatic interaction, makes it a stable catalyst without disrupting the composite structure. Also, the aggregation of the $Cu_2S/Hβcd$ with the layered sheets of rGO can be highly reduced and resulting in the improvement of the conductivity. Thus, the above features resulted in the improved oxidation response current when fabricated over the glassy carbon electrode (GCE). The SR showed sensitive response at a broad linear range of 0.019 to 0.299 $μ$M and 4.28 to 403.14 $μ$M, resulting in a lower limit of detection (LOD) of 1.2 nM or 0.0012 $μ$M and a sensitivity of about 15.9 $μ$A $μM^{-1}$ $cm^{-2}$. The sensor demonstrated excellent selectivity against common interferents, including aminophenol, dopamine, epinephrine, hydroquinone, melatonin, and chlorine. The real sample studies in the biological samples show good recovery values, showing the effectiveness of the as-fabricated sensor. Thus, the cost-efficient and straightforward integration of $Cu_2S/Hβcd-rGO$ will be an outstanding electrocatalyst for detecting SR.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Aravindan Santhan, Kuo Yuan Hwa, Slava V. Rotkin, Cheng-Han Wang, Chun-Wei Ou. 2025-11-06. A copper sulfide-hydroxypropyl $β$-Cyclodextrin-reduced graphene oxide composite for highly sensitive electrochemical detection of 5-hydroxytryptamine in biological samples. https://arxiv.org/abs/2511.04493

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Incommensurate structural and magnetic modulations in potassium-rich cryptomelane, K$_x$Mn$_8$O$_{16}$ ($x\approx1.45$)

Cryptomelane is a hollandite-like material consisting of K$^+$ cations in an $α$-MnO$_2$ tunnel-like crystallographic motif. Cryptomelane with stoichiometry K$_x$Mn$_8$O$_{16}$ ($x\approx1.45$) has been synthesized and its magnetic properties investigated using variable-temperature magnetic susceptibility, heat capacity, and neutron powder diffraction. Three distinct transitions at $T_1=184$\,K, $T_2=54.5$\,K, and $T_3=24$\,K are observed. At $T_1$ there is a subtle tetragonal$\rightarrow$monoclinic transition associated with emergence of a set of non-magnetic superstructure peaks indexable to a $\vec{k}_\mathrm{struc}\approx0.74\vec{c^*}$ incommensurate modulation parallel to the $α$-MnO$_2$ tunnels. Our findings are consistent with a relation previously reported in titanate hollandites, that $x\approx2|\vec{k}_\mathrm{struc}|$. Magnetic Bragg peaks emerge below $T_2=54.5$\,K, and their positions indicate an incommensurate modulated magnetic structure. The model consistent with the data is a dual-$\vec{k}_\mathrm{mag}$ structure with a ferromagnetic $|\vec{k}_\mathrm{mag}|=0$ component and an incommensurate $\vec{k}_\mathrm{mag}\approx0.37\vec{c^*}$, with the latter most likely to be helical. The period of oscillation of the incommensurate magnetic component is in line with predictions based on a Heisenberg spin Hamiltonian [Mandal \textit{et al}. Phys. Rev. B 90, 104420 (2014)]. Below $T_3=24$\,K, there is a magnetic transition, which gives rise to a different set of magnetic Bragg peaks indicative of a highly complex magnetic structure.

cond-mat.mtrl-sci

An anisotropic functional for two-dimensional material systems

Density function theory is the workhorse of modern electronic structure theory. However, its accuracy in practical calculations is limited by the choice of the exchange-correlation potential. In this respect, two-dimensional materials pose a special challenge, as all these materials and their heterostructures have a crucial similarity. The underlying atomic structures are strongly spatially inhomogeneous, implying that current exchange-correlation functionals, that in almost all cases are isotropic, are ill-prepared for an accurate description. We present an anisotropic screened-exchange potential, that remedies this problem and reproduces the band-gap of 2D materials as well as the piecewise linearity of the total energy with fractional occupation number.

cond-mat.mtrl-sci

Thermally-driven reorientation of the Néel vector in altermagnetic MnTe

Altermagnets are novel magnetic systems that possess a spin-polarized electronic band structure without a net magnetic moment, making them promising for device applications. Hexagonal MnTe, a prototypical altermagnet, arguably exhibits the most properties consistent with theoretical predictions, including an anomalous Hall effect despite a vanishing net magnetization, and altermagnetinduced electronic band splitting. However, fundamental questions remain, including why some effects only appear significantly below the magnetic ordering temperature. Here, we resolve this discrepancy by revealing a reorientation of the Néel vector in single-crystalline MnTe. The Néel vector points 30° from the a-axis at low $T$, before aligning directly with the a-axis around $T\simeq 260$ K. We attribute this to single-ion anisotropy, which depends on temperature-dependent lattice parameters. We obtained these results using muon-spin spectroscopy, magnetization measurements, and X-ray diffraction; we show that the findings are consistent with neutron diffraction. Manipulating this effect, for example through strain, could unlock sensitive electronic detection schemes for external stimuli, paving the way for functional altermagnetic devices.

cond-mat.mtrl-sci