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将 CoS 通过化学接枝到 C 上用于氢溢出和存储。

Chemical grafting of CoS onto C for hydrogen spillover and storage.

机构信息

School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, Heilongjiang 150001, PR China.

出版信息

Nanoscale. 2017 Apr 20;9(16):5141-5147. doi: 10.1039/c7nr00581d.

DOI:10.1039/c7nr00581d
PMID:28387401
Abstract

Metal modified C is considered to be a potential hydrogen storage medium due to its high theoretical capacity. Research interest is growing in various hybrid inorganic compounds-C. While the design and synthesis of a novel hybrid inorganic compound-C is difficult to attain, it has been theorized that the atomic hydrogen could transfer from the inorganic compound to the adjacent C surfaces via spillover and surface diffusion. Here, as a proof of concept experiment, we graft CoS onto Cvia a facile high energy ball milling process. The Raman, XPS, XRD, TEM, HTEM and EELS measurements have been conducted to evaluate the composition and structure of the pizza-like hybrid material. In addition, the electrochemical measurements and calculated results demonstrate that the chemical "bridges" (C-S bonds) between these two materials enhance the binding strength and, hence, facilitate the hydriding reaction of C during the hydrogen storage process. As a result, an increased hydrogen storage capacity of 4.03 wt% is achieved, along with a favorable cycling stability of ∼80% after 50 cycles. Excluding the direct hydrogen storage contribution from CoS in the hybrid paper, the hydrogen storage ability of C was enhanced by 5.9× through the hydriding reaction caused by the CoS modifier. Based on these experimental measurements and theoretical calculations, the unique chemical structure reported here could potentially inspire other C-based advanced hybrids.

摘要

金属修饰的 C 被认为是一种有前途的储氢介质,因为其具有很高的理论容量。人们对各种杂化无机化合物-C 产生了越来越多的研究兴趣。虽然设计和合成新型杂化无机化合物-C 具有一定的难度,但有人提出,原子氢可以通过溢出和表面扩散从无机化合物转移到相邻的 C 表面。在这里,作为概念验证实验,我们通过简便的高能球磨工艺将 CoS 接枝到 C 上。已经进行了 Raman、XPS、XRD、TEM、HTEM 和 EELS 测量,以评估这种类似披萨的杂化材料的组成和结构。此外,电化学测量和计算结果表明,这两种材料之间的化学“桥接”(C-S 键)增强了结合强度,从而促进了 C 在储氢过程中的氢化反应。结果,实现了 4.03wt%的储氢容量增加,并且在 50 次循环后具有约 80%的良好循环稳定性。除了杂化纸中 CoS 的直接储氢贡献外,通过 CoS 改性剂引起的氢化反应,C 的储氢能力增强了 5.9 倍。基于这些实验测量和理论计算,这里报道的独特化学结构可能会激发其他基于 C 的先进杂化材料。

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