Evidence map›Paper›PMID 42102194›Full record

ArticleScience advances2026

Ampere-level furfurylamine electrosynthesis enabled by high-density atomic copper sites and a well-engineered electrolysis reactor.

Weiliang Zhou, Qihua Huo, Shuai Qi, Taiyu Liang, Jiao You, Chunyan Shang, Hengpan Yang, Xue Zhang, Lele Peng, Qi Hu and 1 more

Abstract read
In one paragraph

Article in Science advances, 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

11 authors.

Weiliang ZhouCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.ORCID 0009-0007-7133-033X
Qihua HuoCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.
Shuai QiCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.
Taiyu LiangCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.ORCID 0009-0001-8273-8855
Jiao YouCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.
Chunyan ShangCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.ORCID 0000-0002-5763-3920
Hengpan YangCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.ORCID 0000-0001-7087-0536
Xue ZhangCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.ORCID 0000-0003-1913-719X
Lele PengInstitute of Materials Research, Tsinghua Shenzhen International Graduate School Tsinghua University, Shenzhen, Guangdong 518055, People's Republic of China.ORCID 0000-0002-6628-7142
Qi HuCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.ORCID 0000-0002-3885-0444
Chuanxin HeCollege of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, People's Republic of China.ORCID 0000-0002-2254-360X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Furfurylamine is an essential feedstock for diverse agrochemicals and pharmaceuticals; however, industrial-scale thermochemical furfurylamine production is plagued by high energy consumption and considerable greenhouse gas emissions. Here, we propose an electrosynthesis approach for converting biomass-derived furfural to furfurylamine, using nitrate as the nitrogen source under ambient conditions. We observe that single atomic copper (Cu-SA) sites favor the C─N coupling of nitrate-derived hydroxylamine and furfurals over hydroxylamine hydrogenation to ammonia (preferred by Cu subnanoclusters and nanoparticles), endowing Cu-SA with unique advantages in facilitating furfurylamine production. To enable industrial-scale furfurylamine production and suppress by-product formation, we design a single-pass continuous flow reactor with the separate liquid feeding of furfural and alkaline nitrate solutions and construct the highly dense Cu-SA sites. This integration achieves a large current of 2.3 amperes at a cell voltage of 1.9 volts, accompanied by an 84.53% single-pass conversion rate and 100% selectivity toward furfurylamine. Notably, techno-economic analysis demonstrates the profitability of our electrosynthesis furfurylamine route.

Identifiers

PMID42102194
PMCPMC13155300

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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.