Abhishek Lahiri

Dr. Abhishek Lahiri

Department of Chemical Engineering, Brunel University London, Uxbridge UB8 3PH, UK

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 February 2019 in Frontiers in Chemistry
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Abhishek LahiriAbhishek Lahiri
Abhishek Lahiri
GPGiridhar Pulletikurthi
Giridhar Pulletikurthi
FEFrank Endres
Frank Endres
Developing functional materials via electroless deposition, without the need of external energy is a fascinating concept. Electroless deposition can be subcategorized into galvanic displacement reaction, disproportionation reaction, and deposition in presence of reducing agents. Galvanic displacement reaction is a spontaneous reduction process wherein the redox potentials of the metal/metal ion in the electrolyte govern the thermodynamic feasibility of the process. In aqueous solutions, the galvanic displacement reaction takes place according to the redox potentials of the standard electrochemical series. In comparison, in the case of ionic liquids, galvanic displacement reaction can be triggered by forming metal ion complexes with the anions of the ionic liquids. Therefore, the redox potentials in ILs can be different to those of metal complexes in aqueous solutions. In this review, we highlight the progress in the electroless deposition of metals and semiconductors nanostructures, from ionic liquids and their application toward lithium/sodium batteries, and in catalysis.

31 March 2015 in Physical Chemistry Chemical Physics
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Abhishek LahiriAbhishek Lahiri
Abhishek Lahiri
TSThomas J. S. Schubert
Thomas J. S. Schubert
BIBoyan Iliev
Boyan Iliev
FEFrank Endres
Frank Endres
We show using Raman spectroscopy and charge–discharge cycles a stable ionic liquid electrolyte LiTFSI/[Py1.4]FSI for lithium ion batteries.

7 November 2019 in ACS Applied Materials & Interfaces
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Abhishek LahiriAbhishek Lahiri
Abhishek Lahiri
LYLi Yang
Li Yang
GLGuozhu Li
Guozhu Li
FEFrank Endres
Frank Endres

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Ramin KhezriRamin Khezri
Ramin Khezri
SHSoraya Hosseini
Soraya Hosseini
Abhishek LahiriAbhishek Lahiri
Abhishek Lahiri
SMshiva Rezaei motlagh
shiva Rezaei motlagh
MNMai Nguyen
Mai Nguyen
Soorathep KheawhomSoorathep Kheawhom
Soorathep Kheawhom
Zinc–air batteries (ZABs) offer high specific energy and low-cost production. However, rechargeable ZABs suffer from a limited cycle life. This paper reports that potassium persulfate (KPS) additive in an alkaline electrolyte can effectively enhance the performance and electrochemical characteristics of rechargeable zinc–air flow batteries (ZAFBs). Introducing redox additives into electrolytes is an effective approach to promote battery performance. With the addition of 450 ppm KPS, remarkable improvement in anodic currents corresponding to zinc (Zn) dissolution and limited passivation of the Zn surface is observed, thus indicating its strong effect on the redox reaction of Zn. Besides, the addition of 450 ppm KPS reduces the corrosion rate of Zn, enhances surface reactions and decreases the solution resistance. However, excess KPS (900 and 1350 ppm) has a negative effect on rechargeable ZAFBs, which leads to a shorter cycle life and poor cyclability. The rechargeable ZAFB, using 450 ppm KPS, exhibits a highly stable charge/discharge voltage for 800 cycles. Overall, KPS demonstrates great promise for the enhancement of the charge/discharge performance of rechargeable ZABs.

11 January 2017 in The Journal of Physical Chemistry C
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MOMark Olschewski
Mark Olschewski
RGRené Gustus
René Gustus
OHOliver Höfft
Oliver Höfft
Abhishek LahiriAbhishek Lahiri
Abhishek Lahiri
FEFrank Endres
Frank Endres

22 January 2016 in Physical Chemistry Chemical Physics
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Abhishek LahiriAbhishek Lahiri
Abhishek Lahiri
NBNatalia Borisenko
Natalia Borisenko
ABAndriy Borodin
Andriy Borodin
MOMark Olschewski
Mark Olschewski
FEFrank Endres
Frank Endres
The characterisation of the SEI layer revealed that LiTFSI–[Py 1,4 ] is a relatively good ionic liquid based electrolyte for lithium batteries. However modifications in the electrolyte or a different anion might be necessary to improve the stability and composition of the SEI layer.