Alternative Energy Systems Laboratory

Driving tomorrow's energy research today

Tag: abhinav

Introducing Na-sufficient P3-Na0.9Fe0.5Mn0.5O2 as cathode material for Na-ion batteries

An article titled ” Introducing Na-sufficient P3-Na0.9Fe0.5Mn0.5O2 as cathode material for Na-ion batteries ” authored by Abhinav Tripathi, Shibo Xi, Satyanarayana Reddy Gajjela and Palani Balaya has been accepted for publication in Chemical Communications. [DOI:10.1039/D0CC03701J]

Abstract

P3-Na0.9Fe0.5Mn0.5O2 is reported as a new P-type cathode material for Na-ion batteries. P3 structure can accommodate 0.9 mole of Na-ions leading to high discharge capacity of 155 mAh/g and does not require sacrificial salts for full cell operation. Operando X-ray diffraction studies and ex-situ X-ray absorption studies are also reported.

Developing O3 type layered oxide cathode and its application in 18650 commercial type Na-ion batteries – Acceptance for publication

An article titled”Developing O3 type layered oxide cathode and its application in 18650 commercial type Na-ion batteries” authored by A. Tripathi, A. Rudola, S.R. Gajjela, S. Xi and P. Balaya, has been accepted for publication in Journal of Materials Chemistry A. [DOI: 10.1039/c9ta08991h]

Abstract

A novel, water-stable and high energy density cathode material Na0.9Cu0.12Ni0.10Fe0.30Mn0.43Ti0.05O2 (NCNFMT) is reported here along with a thorough understanding of structural events during battery operation. Systematic substitutions are carried out, which lead to increase in specific energy densities of this family of cathodes from 274.6 W h kgcathode−1 (NCFM – Na0.9Cu0.22Fe0.30Mn0.48O2) to 304.2 W h kgcathode−1 (NCFMT – Na0.9Cu0.22Fe0.30Mn0.43Ti0.05O2) and finally to 350.7 W h kgcathode−1 (NCNFMT – Na0.9Cu0.12Ni0.10Fe0.30Mn0.43Ti0.05O2). Operando X-ray diffraction reveals phase transformations and ex situ EXAFS shows the evolution of local environments around transition metals during charge/discharge. Monoclinic distortions in the NCFM material during O3–P3 phase transformations are suppressed by Ti4+ substitution leading to improvements in the cycling performance of NCFMT. Cu–O octahedral sites exhibit huge Jahn–Teller distortion: Ni2+ substitution in place of Cu2+ not only leads to more ordered Ni–O, but it also helps extract more Na ions from the O3 cathode structure, thus boosting the capacity while also showing good cycling stability due to the highly reversible bond-length and local environmental changes as revealed by EXAFS analyses. X-ray photoelectron spectroscopy shows a titanium-rich surface for NCFMT and NCNFMT which helps improve water-stability. The capacity retention after 200 cycles at 0.2C is 84%, 96% and 90% for NCFM, NCFMT and NCNFMT respectively. The delivered storage capacities of NCFM, NCFMT and NCNFMT are 21 mA h g−1, 47 mA h g−1 and 60 mA h g−1 respectively at 3C. 18650 type Na-ion batteries using the NCNFMT cathode material against a hard carbon anode are also reported to demonstrate potential scalability of the NCNFMT cathode and efficacy of a 1 M NaBF4 tetraglyme electrolyte system for the first time. 18650 cells deliver a specific energy density of 62 W h kgtotal_18650_weight−1 with 90% energy efficiency, thus being suitable for large scale energy storage applications.

Experimental and theoretical studies of trisodium-1,3,5- benzene tricarboxylate as a low voltage anode material for sodium ion batteries – Acceptance of publication

An article titled “Experimental and theoretical studies of trisodium-1,3,5- benzene tricarboxylate as a low voltage anode material for sodium ion batteries” authored by A. Tripathi, Y. Chen, H. Padhy, S. Manzhos and P. Balaya, has been accepted for publication in Energy Technology. [DOI: 10.1002/ente.201801030]

Abstract

We report a tricarboxylate based organic compound for Na storage at low voltage, trisodium‐1,3,5‐benzene tricarboxylate (Na3BTC). We explore the effect of increasing the number of carboxyl redox active groups on the aromatic system versus previously reported dicarboxylate‐based Na electrodes. Sodiation and de‐sodiation of this material occur at average voltages of 0.4 V and 0.5 V, respectively, suitable for anode application. The galvanostatic profile of de‐sodiation consists of two plateaus at 0.5 V and 0.2 V. The material delivers a capacity of 250 mAh g‐1 at C/5 rate, with retention of 80% after 100 cycles. It also has an excellent rate capability delivering 100 mAh g‐1 with 75% retention after 1,500 cycles at 10 C rate. Ex‐situ ATR‐FTIR, ex‐situ 1H NMR studies as well as first principles calculations are performed to understand the sodium storage mechanism. The mechanism is found to be different from those previously observed in lithium dicarboxylates and sodium dicarboxylates in that there is apparently almost no charge donation from the inserted Na to the organic moiety.

Skip to toolbar