Engineering oxygen vacancies of cobalt tungstate nanoparticles enable efficient water splitting in alkaline medium

Engineering oxygen vacancies of cobalt tungstate nanoparticles enable efficient water splitting in alkaline medium
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钨酸钴纳米粒子的工程氧空位能够在碱性介质中有效分解水

DOI:
10.1016/j.apcatb.2019.118090
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发表时间:
2019
期刊:
Applied Catalysis B: Environmental
影响因子:
--
通讯作者:
Cai Weiwei
Cai Weiwei
中科院分区:
其他
文献类型:
--
作者:
Luo Fang;Xu Ruizhi;Ma Shuangxiu;Zhang Quan;Hu Hao;Qu Kongang;Xiao Shenglin;Yang Zehui;Cai Weiwei

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开发地球丰富、高效、稳定的水分解电催化剂对于环境友好的能源转换和储存至关重要。在这里,我们报道了一种直径为 8 nm 的缺氧钨酸钴纳米颗粒(CoWO4-x@C)作为析氢反应(HER)和氧还原反应(OER)的高效双功能电催化剂,其表现出与商用 Pt/C 相当的 HER 活性,相对于 RHE 的过电势分别为 32.5 mV 和 46.8 mV,在酸性和碱性介质中分别提供 10 mA cm−2 的电流密度,归因于丰富的氧空位分别促进氢吸附及其相对重组。此外,在 10,000 次潜在循环后,CoWO4-x@C 观察到不可检测的降解,表明其具有高耐久性。同时,CoWO4-x@C在OER测试中仅需要295 mV的过电势即可提供10 mA cm−2,这优于基准IrO2(313 mV)。要实现 10 mA cm−2 的水分解电流密度且 12 小时内没有任何降解,需要 1.57 V 的电压,该电压相对低于 Pt/C-IrO2 (1.59 V)。
Development of earth-abundant, efficient and stable electrocatalysts for water splitting is of crucial importance for environmentally friendly energy conversion and storage. Here, we report an oxygen deficient cobalt tungstate nanoparticles with diameter of 8 nm (CoWO4-x@C) as efficient bifunctional electrocatalyst for hydrogen evolution reaction (HER) and oxygen reduction reaction (OER), which exhibits comparable HER activity to commercial Pt/C with overpotentials of 32.5 mV and 46.8 mV vs. RHE to deliver current density of 10 mA cm−2in acidic and alkaline mediums, respectively, ascribed to the rich oxygen vacancies facilitating the hydrogen adsorption and its relative recombination, respectively. Additionally, undetectable degradation is observed for CoWO4-x@C after 10,000 potential cycles indicating high durability. Meanwhile, CoWO4-x@C requires only 295 mV overpotential to deliver 10 mA cm−2in the OER test, which is better than the benchmarking IrO2(313 mV). 1.57 V comparably lower than Pt/C-IrO2(1.59 V) is required for achieving the water splitting current density of 10 mA cm−2without any degradation for 12 h.