Add like
Add dislike
Add to saved papers

PtNi bimetallic nanoparticles loaded MoS 2 nanosheets: Preparation and electrochemical sensing application for the detection of dopamine and uric acid.

Composite nanomaterials are particularly useful and offer many excellent opportunities for electrochemical sensing application. Depending on the high catalytic activity of bimetallic nanoparticles, the large specific surface area, abundant active edges and co-catalytic function of MoS2 nanosheets, we, for the first time, prepared a novel PtNi bimetallic nanoparticles loaded MoS2 nanosheets (PtNi@MoS2 ) hybrid material by a co-reduction method for the electrochemical sensing application. The nanocomposite is characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS), and then casted on a bare glassy carbon electrode (GCE) to fabricate an electrochemical sensor (PtNi@MoS2 /GCE). The electrochemical investigation showed that the sensor performed good selectivity and wide linear ranges for the simultaneous detection of dopamine (0.5-150 μM) and uric acid (0.5-600 μM). And the detection limits were down to 0.1 μM (S/N = 3) for both analytes.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app