4.6 Article

Atomically thin MoSe2/graphene and WSe2/graphene nanosheets for the highly efficient oxygen reduction reaction

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 3, 期 48, 页码 24397-24404

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ta06909b

关键词

-

资金

  1. National Natural Science Foundation of China [51273032, 91333104, 51402036]
  2. International Science & Technology Cooperation Program of China [2013DFA51000]
  3. Fundamental Research Funds for the Central Universities [DUT15YQ109]
  4. Natural Science Foundation of Anhui Province [KJ2013A079]
  5. State Key Laboratory of Fine Chemicals of China

向作者/读者索取更多资源

As a conceptually new class of 2D materials, inorganic graphene analogue (IGA) ultrathin nanosheets perform an increasingly vital function in various electronic devices. However, the relatively low electrical conductivity of IGA ultrathin nanosheets severely hampers their application as electrode materials in devices. Through in situ synthesis, we report the combination of inorganic graphene and graphene into atomically thin nanosheets as efficient electrocatalysts for the oxygen reduction reaction (ORR). Benefitting from the advantages of both IGAs and reduced graphene oxide, the g-MoSe2 and g-WSe2 nanocomposites showed excellent ORR activity associated with a number of exchanged electrons close to four, which corresponded to the complete reduction of oxygen into water. In particular, the two electrocatalysts exhibited a positive onset potential of -0.02 V (close to that of Pt/C, 0.02 V) and a high kinetic current density (J(K)) of 10.22 mA cm(-2) for g-MoSe2 and 10.77 mA cm(-2) for g-WSe2 at -0.20 V. Compared with commercial Pt/C, these catalysts possess outstanding long-term durability and fuel crossover resistance capacity in alkaline media. Therefore, nanocomposites of inorganic graphene and graphene can be developed into low-cost and efficient alternatives (to the noble metal Pt) to be used as cathodic electrodes in fuel cells.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据