Example of Catalysis Letters format
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Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format
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Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format Example of Catalysis Letters format
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open access Open Access

Catalysis Letters — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Chemistry (all) #115 of 398 down down by 13 ranks
Catalysis #34 of 57 down down by 6 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 1306 Published Papers | 5798 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 13/07/2020
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Related Journals

open access Open Access
recommended Recommended

American Chemical Society

Quality:  
High
CiteRatio: 19.8
SJR: 4.898
SNIP: 2.2
open access Open Access

Elsevier

Quality:  
High
CiteRatio: 7.3
SJR: 0.8
SNIP: 0.868
open access Open Access

Elsevier

Quality:  
High
CiteRatio: 10.2
SJR: 1.397
SNIP: 1.488
open access Open Access

Springer

Quality:  
Good
CiteRatio: 3.6
SJR: 0.554
SNIP: 0.701

Journal Performance & Insights

Impact Factor

CiteRatio

Determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

A measure of average citations received per peer-reviewed paper published in the journal.

2.482

5% from 2018

Impact factor for Catalysis Letters from 2016 - 2019
Year Value
2019 2.482
2018 2.372
2017 2.911
2016 2.799
graph view Graph view
table view Table view

4.4

7% from 2019

CiteRatio for Catalysis Letters from 2016 - 2020
Year Value
2020 4.4
2019 4.1
2018 3.5
2017 3.8
2016 3.7
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 5% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 7% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

0.587

4% from 2019

SJR for Catalysis Letters from 2016 - 2020
Year Value
2020 0.587
2019 0.567
2018 0.622
2017 0.73
2016 0.755
graph view Graph view
table view Table view

0.708

2% from 2019

SNIP for Catalysis Letters from 2016 - 2020
Year Value
2020 0.708
2019 0.694
2018 0.654
2017 0.753
2016 0.773
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 4% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 2% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Catalysis Letters

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Springer

Catalysis Letters

Catalysis Letters is devoted to the development of catalysis and to providing a platform for the exchange of seminal ideas and advances in heterogeneous, homogeneous, and bio-related catalysis. Our aim is to stimulate the cross-fertilization of ideas in order to bring the vari...... Read More

Chemistry

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Last updated on
12 Jul 2020
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ISSN
1011-372X
i
Impact Factor
Medium - 0.92
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Green faq
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Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
SPBASIC
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Citation Type
Author Year
(Blonder et al, 1982)
i
Bibliography Example
Beenakker CWJ (2006) Specular andreev reflection in graphene. Phys Rev Lett 97(6):067,007, URL 10.1103/PhysRevLett.97.067007

Top papers written in this journal

Journal Article DOI: 10.1007/BF00767368
Dehydrogenation and aromatization of methane under non-oxidizing conditions
Linsheng Wang1, Longxiang Tao1, Maosong Xie1, Guifen Xu1, Jiasheng Huang1, Yide Xu1
01 Mar 1993 - Catalysis Letters

Abstract:

The dehydrogenation and aromatization of methane on modified ZSM-5 zeolite catalysts has been studied under non-oxidizing conditions with a fixed bed continuous-flow reactor and with a temperature programmed reactor. The results show that benzene is the only hydrocarbon product of the catalytic conversion of methane at high t... The dehydrogenation and aromatization of methane on modified ZSM-5 zeolite catalysts has been studied under non-oxidizing conditions with a fixed bed continuous-flow reactor and with a temperature programmed reactor. The results show that benzene is the only hydrocarbon product of the catalytic conversion of methane at high temperature (973 K). The catalytic activity of ZSM-5 is greatly improved by incorporating a metal cation (Mo or Zn). H2 and ethene have been directly detected in the products with a mass spectrometer during TPAR. A carbenium ion mechanism for the activation of methane is suggested. read more read less

Topics:

Oxidative coupling of methane (63%)63% related to the paper, Dehydrogenation (57%)57% related to the paper, Methane (55%)55% related to the paper, Hydrocarbon (51%)51% related to the paper, Aromatization (51%)51% related to the paper
738 Citations
Journal Article DOI: 10.1023/A:1019034728816
Photocatalytic O2 evolution under visible light irradiation on BiVO4 in aqueous AgNO3 solution
Akihiko Kudo, Kazuhiro Ueda1, Hideki Kato1, Ikko Mikami1
01 Dec 1998 - Catalysis Letters

Abstract:

BiVO4 with a 2.3 eV band gap showed an activity for O2 evolution from aqueous solutions containing Ag+ as an electron scavenger under visible light irradiation (λ > 520 nm). The quantum yield was 0.5% at 450 nm. BiVO4 with a 2.3 eV band gap showed an activity for O2 evolution from aqueous solutions containing Ag+ as an electron scavenger under visible light irradiation (λ > 520 nm). The quantum yield was 0.5% at 450 nm. read more read less

Topics:

Band gap (52%)52% related to the paper, Aqueous solution (52%)52% related to the paper, Quantum yield (51%)51% related to the paper, Photocatalysis (50%)50% related to the paper
639 Citations
Journal Article DOI: 10.1023/A:1019028229377
Making gold less noble
01 Feb 2000 - Catalysis Letters

Abstract:

Self‐consistent density functional calculations for the adsorption of O and CO on flat and stepped Au(111) surfaces are used to investigate effects which may increase the reactivity of Au. We find that the adsorption energy does not depend on the number of Au layers if there are more than two layers. Steps are found to bind c... Self‐consistent density functional calculations for the adsorption of O and CO on flat and stepped Au(111) surfaces are used to investigate effects which may increase the reactivity of Au. We find that the adsorption energy does not depend on the number of Au layers if there are more than two layers. Steps are found to bind considerably stronger than the (111) terraces, and an expansive strain has the same effect. On this basis we suggest that the unusually large catalytic activity of highly‐dispersed Au particles may in part be due to high step densities on the small particles and/or strain effects due to the mismatch at the Au–support interface. read more read less
612 Citations
Journal Article DOI: 10.1023/A:1019074901578
The mechanism for NOx storage
Erik Fridell1, Hans Persson1, Björn Westerberg1, Louise Olsson1, Magnus Skoglundh1
01 May 2000 - Catalysis Letters

Abstract:

The mechanisms for storing of NOx in platinum-barium-alumina catalysts during lean-rich transients are investigated. Oxidation of NO to NO2 is found to be an important step. NO2 is found to be important for oxidation of the catalyst or of nitrites to form nitrates. NOx is then stored in the form of surface nitrates. FTIR stud... The mechanisms for storing of NOx in platinum-barium-alumina catalysts during lean-rich transients are investigated. Oxidation of NO to NO2 is found to be an important step. NO2 is found to be important for oxidation of the catalyst or of nitrites to form nitrates. NOx is then stored in the form of surface nitrates. FTIR studies show no formation of bulk nitrates in these experiments. read more read less

Topics:

NOx (56%)56% related to the paper
598 Citations
Journal Article DOI: 10.1023/A:1018925008633
The influence of the preparation methods on the catalytic activity of platinum and gold supported on TiO2 for CO oxidation
01 Mar 1997 - Catalysis Letters

Abstract:

The influence of the preparation methods on the catalytic activity for CO oxidation was markedly large for Au-TiO2 and negligible for Pt-TiO2 catalysts. Platinum and gold were deposited on TiO2 by deposition-precipitation (DP), photodeposition (FD) and impregnation (IMP). The DP method gave the most active catalysts for both ... The influence of the preparation methods on the catalytic activity for CO oxidation was markedly large for Au-TiO2 and negligible for Pt-TiO2 catalysts. Platinum and gold were deposited on TiO2 by deposition-precipitation (DP), photodeposition (FD) and impregnation (IMP). The DP method gave the most active catalysts for both Pt and Au. Gold catalysts prepared by DP were active at temperatures below 273 K and showed a much greater activity than Pt catalysts. read more read less

Topics:

Catalysis (60%)60% related to the paper, Platinum (56%)56% related to the paper, Heterogeneous catalysis (55%)55% related to the paper, Organometallic chemistry (51%)51% related to the paper, Transition metal (51%)51% related to the paper
561 Citations
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Catalysis Letters format uses SPBASIC citation style.

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Frequently asked questions

1. Can I write Catalysis Letters in LaTeX?

Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Catalysis Letters guidelines and auto format it.

2. Do you follow the Catalysis Letters guidelines?

Yes, the template is compliant with the Catalysis Letters guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Catalysis Letters?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Catalysis Letters citation style.

4. Can I use the Catalysis Letters templates for free?

Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Catalysis Letters.

5. Can I use a manuscript in Catalysis Letters that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Catalysis Letters that you can download at the end.

6. How long does it usually take you to format my papers in Catalysis Letters?

It only takes a matter of seconds to edit your manuscript. Besides that, our intuitive editor saves you from writing and formatting it in Catalysis Letters.

7. Where can I find the template for the Catalysis Letters?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Catalysis Letters's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

8. Can I reformat my paper to fit the Catalysis Letters's guidelines?

Of course! You can do this using our intuitive editor. It's very easy. If you need help, our support team is always ready to assist you.

9. Catalysis Letters an online tool or is there a desktop version?

SciSpace's Catalysis Letters is currently available as an online tool. We're developing a desktop version, too. You can request (or upvote) any features that you think would be helpful for you and other researchers in the "feature request" section of your account once you've signed up with us.

10. I cannot find my template in your gallery. Can you create it for me like Catalysis Letters?

Sure. You can request any template and we'll have it setup within a few days. You can find the request box in Journal Gallery on the right side bar under the heading, "Couldn't find the format you were looking for like Catalysis Letters?”

11. What is the output that I would get after using Catalysis Letters?

After writing your paper autoformatting in Catalysis Letters, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Catalysis Letters's impact factor high enough that I should try publishing my article there?

To be honest, the answer is no. The impact factor is one of the many elements that determine the quality of a journal. Few of these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Catalysis Letters?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Catalysis Letters. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Catalysis Letters?

The 5 most common citation types in order of usage for Catalysis Letters are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

15. How do I submit my article to the Catalysis Letters?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Catalysis Letters's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Catalysis Letters in Endnote format?

Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Catalysis Letters Endnote style according to Elsevier guidelines.

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I spent hours with MS word for reformatting. It was frustrating - plain and simple. With SciSpace, I can draft my manuscripts and once it is finished I can just submit. In case, I have to submit to another journal it is really just a button click instead of an afternoon of reformatting.

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