Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 206

The DOI matches its Crossref record.

Electrochemical Lithium Storage of Titanate and Titania Nanotubes and Nanorods

Zhang, H., Li, G. R., An, L. P., Yan, T. Y., Gao, X. P., Zhu, H. Y.·2007·The Journal of Physical Chemistry C

Abstract

Layered protonated titanate nanotubes, synthesized via a hydrothermal reaction in alkaline solution, were calcined at different temperatures (200−500 °C) in air to achieve the products of various morphologies and crystal-phase compositions. The microstructure of obtained products was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and N 2 adsorption. The electrochemical lithium storage of these samples was studied by galvanostatic method and cyclic voltammetry. It is found that the protonated titanate nanotubes maintain layered structure below 300 °C and undergo phase transition to a mixture of anatase and TiO 2 (B) with anatase as the main phase between 300 and 500 °C. In addition, the hollow nanotube morphology still remains below 400 °C, but the tubes convert to solid nanorods during the calcination at 500 °C. It is found the nanotubes calcined at 300 and 400 °C have larger surface areas and exhibit relatively large reversible capacity and good reversibility (remain about 200 mA h/g after 80 cycles). Moreover, the electrochemical lithium storage is controlled by the pseudocapacitive effect, the mixed process of both the pseudocapacitive effect, and diffusion-limited reaction, and the diffusion-limited reaction depends on different microstructures of the resulting samples. The relationship among their phase composition, morphology, porous structure, and electrochemical properties is also discussed.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1021/jp0702595

Cites

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cited by

Metadata

Authors
Zhang, H., Li, G. R., An, L. P., Yan, T. Y., Gao, X. P., & Zhu, H. Y.
Venue
The Journal of Physical Chemistry C
Published
2007-04-01
Volume
111
Issue
16
Pages
6143-6148
ISSN
  • 1932-7447 (ISSN-L)
  • 1932-7455
OpenAlex
W2014141870
Cited by
206
References
0
FWCI
17.32
Type
journal article
Language
en
Open access
closed

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.