双功能
材料科学
氧化物
克拉克电极
催化作用
兴奋剂
析氧
电解
氧还原反应
氧气
间质缺损
无机化学
离子
固溶体
氧化还原
氧还原
电极
固体氧
化学工程
晶体缺陷
空位缺陷
燃料电池
格子(音乐)
过渡金属
掺杂剂
作者
Yu Huan,Shou-Xiao Chen,Rui Zeng,Tao Wei,Dehua Dong,Xun Hu,Yunhui Huang
标识
DOI:10.1002/aenm.201901573
摘要
Abstract Unveiling the intrinsic effects of Ruddlesden‐Popper (RP) series A n +1 B n O 3 n +1 (A = La, B = Ni, Co, Mn, Cu, n = 1, 2 and 3) catalysts is essential in order to optimize the activity of oxygen reduction reaction (ORR) and evolution reaction (OER). Here, it is demonstrated that the oxygen vacancy is not the key point for RP to realize high ORR and OER activity at high temperature. Instead, interstitial O 2− with high concentration and fast migration, and lattice oxygen with high activity are favorable for the high‐temperature catalytic activity. Aliovalent cation doping is an effective strategy to modify the catalytic activity. For the RP catalysts, low‐valence ion doping does not introduce oxygen vacancies, which suppresses the activity of lattice oxygen and decreases the interstitial O 2− concentration; whereas high‐valence ion doping enhances the interstitial O 2– concentration and the lattice oxygen activity. The evaluations of six RP series (La 2 NiO 4 , La 2 CoO 4 , La 3 Co 2 O 7 , La 4 Ni 3 O 10 , La 2 MnO 4 , and La 2 CuO 4 based) and twenty samples as oxygen electrodes for solid oxide fuel cells (SOFCs) and solid oxide electrolysis cells (SOECs) demonstrate that this finding is applicable to all the selected RP series.
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