尿素
光催化
催化作用
产量(工程)
吸附
材料科学
兴奋剂
化学工程
化学
量子产额
介孔材料
光化学
电子转移
纳米技术
可持续生产
极化(电化学)
无机化学
可持续能源
高能
作者
Jiamin Ma,Yang Gao,Wanning Zhang,Lu Han,Shunai Che,Yuxi Fang
标识
DOI:10.1002/anie.202525892
摘要
ABSTRACT Direct synthesis of urea through photocatalytic N 2 and CO 2 reduction (PNCR) offers a sustainable approach to mitigate CO 2 emissions and reduce energy consumption from urea production for industry and agriculture. However, achieving high yield of urea is limited by the high energy barrier for co‐reduction of N 2 and CO 2 with subsequent C–N coupling. Herein, we propose that the spin polarization of chiral mesostructured Mo doped Bi 2 WO 6 (CMMB) can facilitate the formation of triplet 3 NOH by regulating the parallel electron spin alignment and promote the separation and transfer of photogenerated carriers, leading to enhanced C–N formation. The incorporation of Mo sites into Bi 2 WO 6 promotes the adsorption and activation of N 2 . A state‐of‐the‐art urea yield was achieved without additives via PNCR on CMMB, surpassing the best‐reported inorganic catalyst by a significant margin. This study provides an effective strategy for designing catalyst structures for the green synthesis of organonitrogen compounds.
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