Single-Atom Ni Supported on TiO2 for Catalyzing Hydrogen Storage in MgH2

脱氢 化学 催化作用 氢气储存 解吸 动力学 活化能 Atom(片上系统) 化学工程 物理化学 有机化学 吸附 计算机科学 物理 量子力学 工程类 嵌入式系统
作者
Jiyue Zhang,Wenda Wang,Xiaowei Chen,Jinlong Jin,Xiaojun Yan,Jianmei Huang
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:146 (15): 10432-10442 被引量:176
标识
DOI:10.1021/jacs.3c13970
摘要

As an efficient and clean energy carrier, hydrogen is expected to play a key role in future energy systems. However, hydrogen-storage technology must be safe with a high hydrogen-storage density, which is difficult to achieve. MgH 2 is a promising solid-state hydrogen-storage material owing to its large hydrogen-storage capacity (7.6 wt %) and excellent reversibility, but its large-scale utilization is restricted by slow hydrogen-desorption kinetics. Although catalysts can improve the hydrogen-storage kinetics of MgH 2, they reduce the hydrogen-storage capacity. Single-atom catalysts maximize the atom utilization ratio and the number of interfacial sites to boost the catalytic activity, while easy aggregation at high temperatures limits further application. Herein, we designed a single-atom Ni-loaded TiO 2 catalyst with superior thermal stability and catalytic activity. The optimized 15wt%-Ni 0.034 @TiO 2 catalyst reduced the onset dehydrogenation temperature of MgH 2 to 200 °C. At 300 °C, the H 2 released and absorbed 4.6 wt % within 5 min and 6.53 wt % within 10 s, respectively. The apparent activation energies of MgH 2 dehydrogenation and hydrogenation were reduced to 64.35 and 35.17 kJ/mol of H 2, respectively. Even after 100 cycles of hydrogenation and dehydrogenation, there was still a capacity retention rate of 97.26%. The superior catalytic effect is attributed to the highly synergistic catalytic activity of single-atom Ni, numerous oxygen vacancies, and multivalent Ti x+ in the TiO 2 support, in which the single-atom Ni plays the dominant role, accelerating electron transfer between Mg 2+ and H – and weakening the Mg–H bonds. This work paves the way for superior hydrogen-storage materials for practical unitization and also extends the application of single-atom catalysis in high-temperature solid-state reactions.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
窖藏喜之郎完成签到 ,获得积分10
1秒前
醉熏的烤鸡完成签到,获得积分10
1秒前
起气球发布了新的文献求助10
1秒前
2秒前
2秒前
Lee发布了新的文献求助10
2秒前
3秒前
文6完成签到 ,获得积分10
3秒前
4秒前
林距离完成签到 ,获得积分10
4秒前
lilongcheng完成签到,获得积分10
4秒前
赘婿应助ccccchen采纳,获得10
5秒前
赟yun完成签到,获得积分0
5秒前
科研通AI6.2应助二十八时采纳,获得10
5秒前
眼睛大的书易完成签到,获得积分10
5秒前
竹蜻蜓完成签到,获得积分10
5秒前
路尚远应助orange采纳,获得10
6秒前
华仔应助Leo采纳,获得10
6秒前
7秒前
7秒前
好好完成签到,获得积分10
7秒前
佰斯特威应助李瑾玥采纳,获得10
8秒前
佰斯特威应助李瑾玥采纳,获得10
8秒前
8秒前
xiaoyao发布了新的文献求助10
8秒前
9秒前
天真的音完成签到,获得积分10
9秒前
kiki发布了新的文献求助10
9秒前
Xx发布了新的文献求助10
10秒前
苏打水518完成签到,获得积分10
11秒前
11秒前
文6发布了新的文献求助10
11秒前
研友_VZG7GZ应助独特的幼菱采纳,获得10
11秒前
12秒前
13秒前
DengLipan应助安详忆梅采纳,获得10
14秒前
徐继军完成签到 ,获得积分10
15秒前
15秒前
小芳发布了新的文献求助10
16秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Governing Growth: Us Industrial Policy from Hamilton to Trump 500
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
Synthesis of P-Chiral Phosphine Ligands and Their Applications in Asymmetric Catalysis 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7624552
求助须知:如何正确求助?哪些是违规求助? 9199667
关于积分的说明 19723259
捐赠科研通 7195607
什么是DOI,文献DOI怎么找? 3273562
关于科研通互助平台的介绍 2435728
邀请新用户注册赠送积分活动 2269409