水解
复合数
化学工程
动力学
化学
氢
材料科学
产量(工程)
有机化学
复合材料
物理
量子力学
工程类
作者
Yongyang Zhu,Liming Zeng,Daifeng Wu,Shun Wang,Qing Zhou,Renheng Tang,Chi Pong Tsui,Zheng‐Long Xu,Xu‐Sheng Yang,K.C. Chan
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-02-28
卷期号:24 (10): 3221-3230
被引量:1
标识
DOI:10.1021/acs.nanolett.4c00115
摘要
The hydrolysis of hydrides, represented by MgH2, delivers substantial capacity and presents an appealing prospect for an on-site hydrogen supply. However, the sluggish hydrolysis kinetics and low hydrogen yield of MgH2 caused by the formation of a passivation Mg(OH)2 layer hinder its practical application. Herein, we present a dual strategy encompassing microstructural design and compounding, leading to the successful synthesis of a core–shell-like nanostructured MgH2@Mg(BH4)2 composite, which demonstrates excellent hydrolysis performance. Specifically, the optimal composite with a low Ea of 9.05 kJ mol–1 releases 2027.7 mL g–1 H2 in 60 min, and its hydrolysis rate escalates to 1356.7 mL g–1 min–1 H2 during the first minute at room temperature. The nanocoating Mg(BH4)2 plays a key role in enhancing the hydrolysis kinetics through the release of heat and the formation of local concentration of Mg2+ field after its hydrolysis. This work offers an innovative concept for the design of hydrolysis materials.
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