Xu Xiaomin, Pan Yangli, Zhong Yijun, Shi Chenliang, Guan Daqin, Ge Lei, Hu Zhiwei, Chin Yi-Ying, Lin Hong-Ji, Chen Chien-Te, Wang Hao, Jiang San Ping, Shao Zongping
WA School of Mines: Minerals, Energy and Chemical Engineering (WASM-MECE), Curtin University, Perth, WA, 6102, Australia.
Centre for Future Materials, University of Southern Queensland, Springfield Central, QLD, 4300, Australia.
Adv Sci (Weinh). 2022 May;9(14):e2200530. doi: 10.1002/advs.202200530. Epub 2022 Mar 20.
Oxygen evolution reaction (OER) is a key half-reaction in many electrochemical transformations, and efficient electrocatalysts are critical to improve its kinetics which is typically sluggish due to its multielectron-transfer nature. Perovskite oxides are a popular category of OER catalysts, while their activity remains insufficient under the conventional adsorbate evolution reaction scheme where scaling relations limit activity enhancement. The lattice oxygen-mediated mechanism (LOM) has been recently reported to overcome such scaling relations and boost the OER catalysis over several doped perovskite catalysts. However, direct evidence supporting the LOM participation is still very little because the doping strategy applied would introduce additional active sites that may mask the real reaction mechanism. Herein, a dopant-free, cation deficiency manipulation strategy to tailor the bulk diffusion properties of perovskites without affecting their surface properties is reported, providing a perfect platform for studying the contribution of LOM to OER catalysis. Further optimizing the A-site deficiency achieves a perovskite candidate with excellent intrinsic OER activity, which also demonstrates outstanding performance in rechargeable Zn-air batteries and water electrolyzers. These findings not only corroborate the key role of LOM in OER electrocatalysis, but also provide an effective way for the rational design of better catalyst materials for clean energy technologies.
析氧反应(OER)是许多电化学转化过程中的关键半反应,高效的电催化剂对于改善其动力学至关重要,由于其多电子转移性质,该动力学通常较为缓慢。钙钛矿氧化物是一类常见的OER催化剂,然而在传统的吸附质演化反应方案中,其活性仍然不足,在该方案中,比例关系限制了活性的提高。最近有报道称,晶格氧介导机制(LOM)可以克服这种比例关系,并提高几种掺杂钙钛矿催化剂的OER催化性能。然而,支持LOM参与的直接证据仍然很少,因为所采用的掺杂策略会引入额外的活性位点,这可能会掩盖真正的反应机制。在此,报道了一种无掺杂剂的阳离子缺陷调控策略,用于调整钙钛矿的体扩散性质而不影响其表面性质,为研究LOM对OER催化的贡献提供了一个理想的平台。进一步优化A位缺陷得到了一种具有优异本征OER活性的钙钛矿候选物,其在可充电锌空气电池和水电解槽中也表现出优异的性能。这些发现不仅证实了LOM在OER电催化中的关键作用,还为合理设计用于清洁能源技术的更好催化剂材料提供了一条有效途径。