电催化剂
催化作用
硝酸盐
氨生产
氨
化学
无机化学
电化学
有机化学
电极
物理化学
作者
Yuefei Li,Yuan Tan,Mingkai Zhang,Jun Hu,Zhong Chen,Laisuo Su,Jiayuan Li
标识
DOI:10.1002/anie.202411068
摘要
Electrochemical conversion from nitrate to ammonia is a key step in sustainable ammonia production. However, it suffers from low productive efficiency or high energy consumption due to a lack of desired electrocatalysts. Here we report nickel cobalt phosphide (NiCoP) catalysts for nitrate‐to‐ammonia electrocatalysis that display a record‐high catalytic current density of −702±7 mA cm−2, ammonia production rate of 5415±26 mmol gcat−1 h−1 and Faraday efficiency of 99.7±0.2 % at −0.3 V vs. RHE, affording the estimated energy consumption as low as 22.7 kWh kgammonia−1. Theoretical and experimental results reveal that these catalysts benefit from hydrogen poisoning effects under low overpotentials, which leave behind catalytically inert adsorbed hydrogen species (HI*) at Co‐hollow sites and thereupon enable ideally reactive HII* at secondary Co−P sites. The dimerization between HI* and HII* for H2 evolution is blocked due to the catalytic inertia of HI* thereby the HII* drives nitrate hydrogenation timely. With these catalysts, the continuous ammonia production is further shown in an electrolyser with a real energy consumption of 18.9 kWh kgammonia−1.
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