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3Co 1.5Fe 1.5O 10-δ]]>

机译:<! FE 1.5 O 10-Δ]]>

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摘要

AbstractTo accelerate the kinetics of oxygen evolution reaction (OER) on H2O oxidation regarding the energy conversion and storage approaches, the discovery and design of desirable cost-effective and highly efficient electrocatalysts is of prime importance. This study demonstrates a novel layered perovskite via Co-doping strategy, i.e. LaSr3Co1.5Fe1.5O10-δ, which possesses significantly higher electrocatalytic activity, considerably lower overpotential and Tafel slope, remarkably higher mass activity (MA) and specific activity (SA) together with a better long-term stability than the undoped parent perovskite, the state-of-the-art IrO2and the most active Ba0.5Sr0.5Co0.8Fe0.2O3-δ(BSCF) under harsh OER cycling conditions in alkaline solution. These merits mainly originate from the presence of partial oxidation of surface Co3+to Co4+in LaSr3Co1.5Fe1.5O10-δ, an appropriate possible structure-dependent position of Op-band centre to the Fermi level and an increased amount of highly oxidative oxygen species O22-/O-in conjunction with a strong OH-adsorption and O2des
机译:<![cdata [ 抽象 加速H 2 o对能量转换和储存方法的氧化,理想的成本效益和高效电催化剂的发现和设计是素质的重要性。本研究通过共掺杂策略演示了一种新颖的分层钙钛矿,即LASR 3 CO 1.5 FE 1.5 O 10-Δ,其具有显着更高的电催化活动,具有显着更高的过电容和Tafel斜率,较高的质量活动(MA)和特定活动(SA)以及比未掺杂的父母佩罗夫斯基特更好的长期稳定性,最先进的IRO 2 和最活跃的ba 0.5 SR 0.5 CO 0.8 FE 0.2 O 3-Δ(BSCF)在碱性溶液中的苛刻oer循环条件下。这些优点主要源于表面CO的部分氧化 3 + to co <​​ce:sup =“post”> 4 + 在LASR 3 CO 1.5 FE 1.5 O 10-Δ,适当的O P - 带的结构相关位置中心到FERMI水平和高氧化氧气量的增加量O 2 2 - / o - 与强oh - 吸附和o 2 DES

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