Evidence map›Paper›PMID 40841538›Full record

ArticleNature communications2025

Decoding technical multi-promoted ammonia synthesis catalysts.

Luis Sandoval-Díaz, Raoul Blume, Kassiogé Dembélé, Jan Folke, Maxime Boniface, Frank Girgsdies, Adnan Hammud, Zahra Gheisari, Danail Ivanov, René Eckert and 7 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. The role of the NNature communications · 2026
    Article
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Luis Sandoval-DíazDepartment of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck-Society, Berlin, Germany. lesandovaldi@fhi-berlin.mpg.de.ORCID http://orcid.org/0009-0003-6265-0623
Raoul BlumeDepartment of Heterogeneous Reactions, Max Planck Institute for Chemical Energy Conversion, Mülheim an der Ruhr, Germany.
Kassiogé DembéléDepartment of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck-Society, Berlin, Germany.ORCID http://orcid.org/0000-0001-5630-0414
Jan FolkeDepartment of Heterogeneous Reactions, Max Planck Institute for Chemical Energy Conversion, Mülheim an der Ruhr, Germany.
Maxime BonifaceDepartment of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck-Society, Berlin, Germany.
Frank GirgsdiesDepartment of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck-Society, Berlin, Germany.ORCID http://orcid.org/0000-0002-0994-0686
Adnan HammudDepartment of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck-Society, Berlin, Germany.ORCID http://orcid.org/0000-0001-5580-7985
Zahra GheisariDepartment of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck-Society, Berlin, Germany.
Danail IvanovDepartment of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck-Society, Berlin, Germany.
René EckertClariant Produkte (Deutschland) GmbH, Heufeld, Germany.
Stephan ReitmeierClariant Produkte (Deutschland) GmbH, Heufeld, Germany.
Andreas ReitzmannClariant Produkte (Deutschland) GmbH, Heufeld, Germany.
Robert SchlöglDepartment of Interface Science, Fritz-Haber-Institute of the Max-Planck-Society, Berlin, Germany.
Beatriz Roldan CuenyaDepartment of Interface Science, Fritz-Haber-Institute of the Max-Planck-Society, Berlin, Germany.ORCID http://orcid.org/0000-0002-8025-307X
Holger RulandDepartment of Heterogeneous Reactions, Max Planck Institute for Chemical Energy Conversion, Mülheim an der Ruhr, Germany.ORCID http://orcid.org/0000-0001-5530-1458
Axel Knop-GerickeDepartment of Heterogeneous Reactions, Max Planck Institute for Chemical Energy Conversion, Mülheim an der Ruhr, Germany.
Thomas LunkenbeinDepartment of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck-Society, Berlin, Germany. lunkenbein@fhi-berlin.mpg.de.ORCID http://orcid.org/0000-0002-8957-4216

Funding

Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 03EW0015BDeutsche Forschungsgemeinschaft (German Research Foundation) EXC 2089/1-390776260
6 · The paper itself

Abstract

Ammonia is industrially produced by the Haber-Bosch process over a fused, multi-promoted iron-based catalyst. Current knowledge about the reaction has been derived from model systems of reduced structural complexity, impeding any clear-cut structure-activity correlation relevant for the industrial counterpart. Here, we unveil the structural evolution of complex, technical, multi-promoted ammonia synthesis catalysts by operando scanning electron microscopy and near-ambient pressure X-ray photoelectron spectroscopy. We highlight that the activation is the critical step in which the catalyst is formed and decode the pivotal role of the promoters. We discover that the active structure consists of a nanodispersion of Fe covered by mobile K-containing adsorbates, so called "ammonia K". The porous catalyst is stabilized by mineral cementitious phases containing oxides of Al, Si, Ca, and Fe. The synergism between the different promoters contributes simultaneously to the structural stability, hierarchical architecture, catalytic activity, and poisoning resistance. The confluence of these aspects is the key for the superior performance of technical catalyst formulations.

Identifiers

PMID40841538
PMCPMC12370944

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.