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Ultrathin amorphous cobalt–vanadium hydr(oxy)oxide catalysts for the oxygen evolution reaction†
Energy & Environmental Science ( IF 32.5 ) Pub Date : 2018-04-13 00:00:00 , DOI: 10.1039/c8ee00611c
Juzhe Liu 1, 2, 3, 4, 5 , Yongfei Ji 6, 7, 8, 9, 10 , Jianwei Nai 1, 2, 3, 4, 5 , Xiaogang Niu 1, 2, 3, 4, 5 , Yi Luo 6, 7, 8, 9, 10 , Lin Guo 1, 2, 3, 4, 5 , Shihe Yang 5, 11, 12, 13, 14
Affiliation  

Cost efficient and long-term stable catalysts are in great demand for the oxygen evolution reaction (OER), a key process involved in water splitting cells and metal–air batteries. Here, we demonstrate that the ultrathin amorphous cobalt–vanadium hydr(oxy)oxide we synthesized is a highly promising electrocatalytic material for the OER with a low overpotential of 0.250 V (even lower down to 0.215 V when supported on Au foam) at 10 mA cm−2 and a long stable operation time (170 h) in alkaline media. In combination with in situ X-ray absorption spectral characterization and first-principles simulations, we reveal that the ultrathin, amorphous and alloyed structural characteristics have enabled its facile transformation to the desirable active phase, leading to a dramatically enhanced catalytic activity. Our finding highlights the remarkable advantages of the two-dimensional amorphous material and sheds new light on the design of high-performance electrocatalysts.

中文翻译:

超薄无定形钴氧钒氧化钒催化剂,用于氧气释放反应

具有成本效益和长期稳定的催化剂对氧气析出反应(OER)有着巨大的需求,氧气析出反应是水分离电池和金属空气电池所涉及的关键过程。在这里,我们证明了我们合成的超薄无定形钴-氢氧化氧钒钒是一种极有希望的OER电催化材料,在10 mA时具有0.250 V的低过电势(当负载在Au泡沫上时甚至更低,甚至低至0.215 V) cm -2,在碱性介质中稳定的工作时间长(170 h)。与原位结合X射线吸收光谱表征和第一性原理模拟表明,超薄,无定形和合金结构特征使其能够轻松转变为所需的活性相,从而大大提高了催化活性。我们的发现突出了二维无定形材料的显着优势,并为高性能电催化剂的设计提供了新的思路。
更新日期:2018-04-13
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