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锰掺杂调控碳酸钴羟基的电子-形态双重结构以构筑高效稳定的全水解双功能电催化剂

Electronic and Morphological Dual Modulation of Cobalt Carbonate Hydroxides by Mn Doping toward Highly Efficient and Stable Bifunctional Electrocatalysts for Overall Water Splitting.

机构信息

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences (CAS) , Beijing 100190, China.

Laboratory of Functionalized Molecular Solids, Ministry of Education, Anhui Key Laboratory of Chemo/Biosensing, Laboratory of Optical Probes and Bioelectrocatalysis, College of Chemistry and Materials Science, Anhui Normal University , Wuhu 241000, China.

出版信息

J Am Chem Soc. 2017 Jun 21;139(24):8320-8328. doi: 10.1021/jacs.7b03507. Epub 2017 Jun 13.

Abstract

Developing bifunctional efficient and durable non-noble electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is highly desirable and challenging for overall water splitting. Herein, Co-Mn carbonate hydroxide (CoMnCH) nanosheet arrays with controllable morphology and composition were developed on nickel foam (NF) as such a bifunctional electrocatalyst. It is discovered that Mn doping in CoCH can simultaneously modulate the nanosheet morphology to significantly increase the electrochemical active surface area for exposing more accessible active sites and tune the electronic structure of Co center to effectively boost its intrinsic activity. As a result, the optimized CoMnCH/NF electrode exhibits unprecedented OER activity with an ultralow overpotential of 294 mV at 30 mA cm, compared with all reported metal carbonate hydroxides. Benefited from 3D open nanosheet array topographic structure with tight contact between nanosheets and NF, it is able to deliver a high and stable current density of 1000 mA cm at only an overpotential of 462 mV with no interference from high-flux oxygen evolution. Despite no reports about effective HER on metal carbonate hydroxides yet, the small overpotential of 180 mV at 10 mA cm for HER can be also achieved on CoMnCH/NF by the dual modulation of Mn doping. This offers a two-electrode electrolyzer using bifunctional CoMnCH/NF as both anode and cathode to perform stable overall water splitting with a cell voltage of only 1.68 V at 10 mA cm. These findings may open up opportunities to explore other multimetal carbonate hydroxides as practical bifunctional electrocatalysts for scale-up water electrolysis.

摘要

开发用于析氧反应(OER)和析氢反应(HER)的双功能高效且耐用的非贵金属电催化剂对于整体水分解是非常理想和具有挑战性的。在此,在镍泡沫(NF)上开发了具有可控形态和组成的 Co-Mn 碳酸盐氢氧化物(CoMnCH)纳米片阵列作为这种双功能电催化剂。研究发现,Mn 在 CoCH 中的掺杂可以同时调节纳米片形态,从而显著增加电化学活性表面积,以暴露更多可及的活性位点,并调整 Co 中心的电子结构,从而有效地提高其本征活性。结果,优化后的 CoMnCH/NF 电极表现出前所未有的 OER 活性,在 30 mA cm 时的过电位仅为 294 mV,优于所有报道的金属碳酸盐氢氧化物。得益于具有纳米片之间紧密接触的 3D 开放纳米片阵列形貌结构,它能够在仅 462 mV 的过电位下提供高且稳定的电流密度 1000 mA cm,而不受高通量氧气析出的干扰。尽管目前尚无关于金属碳酸盐氢氧化物上有效 HER 的报道,但通过 Mn 掺杂的双重调节,在 CoMnCH/NF 上也可以实现小过电位 180 mV 时 10 mA cm 的 HER。这提供了一种使用双功能 CoMnCH/NF 作为阳极和阴极的两电极电解槽,以仅 1.68 V 的电池电压在 10 mA cm 下稳定地进行整体水分解。这些发现可能为探索其他多金属碳酸盐氢氧化物作为实用的双功能电催化剂用于规模化水电解开辟了机会。

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