Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu, Sichuan, 610064, China.
Adv Mater. 2023 Jan;35(1):e2207305. doi: 10.1002/adma.202207305. Epub 2022 Nov 28.
Developing highly active and selective electrocatalysts for electrochemical nitrate reduction reaction (NITRR) is very important for synthesizing recyclable ammonia (NH ) in an economic and environmentally friendly manner. Despite some encouraging progress, their activity and selectivity have been remarkably slower than expected. In this manuscript, mesoporous palladium-nonmetal (meso-PdX) nanocubes (NCs) are reported as a new series of highly efficient electrocatalysts for selective nitrate reduction reaction (NITRR) electrocatalysis to NH . The samples feature uniformly alloyed compositions and highly penetrated mesopores with abundant highly active sites and optimized electronic structures. The best meso-PdN NCs hold an outstanding NITRR activity and selectivity with a remarkable NH Faradaic efficiency of 96.1% and a yield rate of 3760 µg h mg , suppressing the state-of-the-art electrocatalysts. Meanwhile, meso-PdN NCs are electrocatalytically stable, retaining well the activity and selectivity of NO -to-NH electrocatalysis for more than 20 cycles. Detailed mechanism studies ascribe the superior performance to combined compositional and structural synergies of meso-PdN NCs that not only promote the adsorption (reactivity) of NO and the desorption of NH but also increase the retention time of key intermediates for the deeper NITRR electrocatalysis to NH through an eight-electron pathway.
开发高效且选择性的电化学硝酸盐还原反应(NITRR)电催化剂对于以经济和环保的方式合成可回收氨(NH )非常重要。尽管已经取得了一些令人鼓舞的进展,但它们的活性和选择性的提升速度却明显慢于预期。在本文中,报道了一系列新型高效电催化剂——介孔钯-非金属(meso-PdX)纳米立方(NCs),用于选择性硝酸盐还原反应(NITRR)电催化合成 NH 。这些样品具有均匀的合金组成和高度穿透的介孔,具有丰富的高活性位点和优化的电子结构。最佳的介孔 PdN NCs 具有出色的 NITRR 活性和选择性,NH 的法拉第效率高达 96.1%,产率为 3760µg h mg ,优于现有技术水平的电催化剂。同时,介孔 PdN NCs 具有电催化稳定性,在超过 20 个循环中保持良好的 NO -到-NH 电催化活性和选择性。详细的机理研究将优异的性能归因于介孔 PdN NCs 的协同组合效应,这种协同组合效应不仅促进了 NO 的吸附(反应性)和 NH 的解吸,而且通过八电子途径增加了关键中间体的保留时间,从而促进了更深层次的 NITRR 电催化合成 NH 。