Evidence map›Paper›PMID 41730889›Full record

ArticleNature communications2026

Crystallization-assisted water adsorption in amorphous molecular adsorbents.

Feng Xie, Liang Yu, Simon Teat, Jocelyn Shutak, Trevor Jenkins, Jiaqi Liu, Fu-An Guo, Lulu Ma, Timo Thonhauser, Kui Tan and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Feng XieDepartment of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ, USA.ORCID http://orcid.org/0000-0002-4273-8770
Liang YuHoffmann Institute of Advanced Materials, Shenzhen Polytechnic University, Guangdong, PR China.
Simon TeatAdvanced Light Source, Lawrence Berkeley National Laboratory, California, CA, USA.ORCID http://orcid.org/0000-0001-9515-2602
Jocelyn ShutakDepartment of Chemistry, University of North Texas, Denton, TX, USA.
Trevor JenkinsDepartment of Physics and Center for Functional Materials, Wake Forest University, Winston-Salem, NC, USA.
Jiaqi LiuHoffmann Institute of Advanced Materials, Shenzhen Polytechnic University, Guangdong, PR China.
Fu-An GuoHoffmann Institute of Advanced Materials, Shenzhen Polytechnic University, Guangdong, PR China.
Lulu MaHoffmann Institute of Advanced Materials, Shenzhen Polytechnic University, Guangdong, PR China.
Timo ThonhauserDepartment of Physics and Center for Functional Materials, Wake Forest University, Winston-Salem, NC, USA.ORCID http://orcid.org/0000-0003-4771-7511
Kui TanDepartment of Chemistry, University of North Texas, Denton, TX, USA.
Hao WangHoffmann Institute of Advanced Materials, Shenzhen Polytechnic University, Guangdong, PR China. wanghao@szpu.edu.cn.ORCID http://orcid.org/0000-0001-7732-778X
Jing LiDepartment of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ, USA. jingli@rutgers.edu.ORCID http://orcid.org/0000-0001-7792-4322

Funding

U.S. Department of Energy (DOE) DE-AC02-05CH11231U.S. Department of Energy (DOE) DE-SC0019902
6 · The paper itself

Abstract

Efficient and stable water adsorbents are essential for removing moisture from natural gas and olefins during their production. Industrial desiccants such as alumina and zeolites require high regeneration temperatures, while metal-organic frameworks often suffer from limited long-term stability and reusability. Here, we introduce a new type of molecular desiccants (M-PyC) that, in principle, can be reused indefinitely. These simple molecular coordination complexes undergo fully reversible phase transitions between crystalline and amorphous states through the decoordination (bond breaking) and recoordination (bond reforming) of water molecules. They exhibit high water uptake (30 wt%) and superb selectivity, excluding hydrocarbons entirely. Their effectiveness for dehydration, combined with low regeneration temperature, fast desorption kinetics, low-cost and green synthesis, easy scalability to kilogram quantities, and essentially unlimited recyclability, makes them truly competitive dehydration agents for industrial separations. The use of amorphous molecular adsorbents, where crystallinity and porosity are no longer stringent requirements, and the adsorption-desorption process entirely under ambient air, offers a conceptually different approach to adsorption-based separation science and potentially realistic solution to the long-standing challenge of sustained stability in coordinate-bonded adsorbents.

Identifiers

PMID41730889
PMCPMC13039353

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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.