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用于从一水合肼中高容量制氢的无贵金属Ni-W-O衍生催化剂

Noble-Metal-Free Ni-W-O-Derived Catalysts for High-Capacity Hydrogen Production from Hydrazine Monohydrate.

作者信息

Shi Qing, Zhang Deng-Xue, Yin Hui, Qiu Yu-Ping, Zhou Liang-Liang, Chen Chen, Wu Hui, Wang Ping

机构信息

School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, P.R. China.

NIST Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland 20899-6102, United States.

出版信息

ACS Sustain Chem Eng. 2020;8(14). doi: 10.1021/acssuschemeng.9b07782.

Abstract

Development of active and earth-abundant catalysts is pivotal to render hydrazine monohydrate (NH·HO) viable as a hydrogen carrier. Herein, we report the synthesis of noble-metal-free Ni-W-O-derived catalysts using a hydrothermal method in combination with reductive annealing treatment. Interestingly, the thus-prepared Ni-based catalysts exhibit remarkably distinct catalytic properties toward NH·HO decomposition depending upon the annealing temperature. From a systematic phase/microstructure/chemical state characterization and the first-principles calculations, we found that the variation of the apparent catalytic properties of these Ni-based catalysts should stem from the formation of different Ni-W alloys with distinct intrinsic activity, selectivity, and distribution state. The thereby chosen Ni-W alloy nanocomposite catalyst prepared under an optimized condition showed high activity, nearly 100% selectivity, and excellent stability toward NH·HO decomposition for hydrogen production. Furthermore, this noble-metal-free catalyst enables rapid hydrogen production from commercially available NH·HO solution with an intriguingly high hydrogen capacity of 6.28 wt % and a satisfactory dynamic response property. These results are inspiring and momentous for promoting the use of the NH·HO-based H source systems.

摘要

开发活性且储量丰富的催化剂对于使水合肼(NH·HO)成为可行的氢载体至关重要。在此,我们报告了使用水热法结合还原退火处理合成无贵金属的Ni-W-O衍生催化剂。有趣的是,如此制备的镍基催化剂对NH·HO分解表现出明显不同的催化性能,这取决于退火温度。通过系统的相/微观结构/化学状态表征和第一性原理计算,我们发现这些镍基催化剂表观催化性能的变化应源于形成具有不同本征活性、选择性和分布状态的不同Ni-W合金。在优化条件下制备的所选Ni-W合金纳米复合催化剂对NH·HO分解制氢表现出高活性、近100%的选择性和优异的稳定性。此外,这种无贵金属催化剂能够从市售的NH·HO溶液中快速制氢,具有高达6.28 wt%的惊人高氢容量和令人满意的动态响应性能。这些结果对于推动基于NH·HO的氢源系统的应用具有启发性和重要意义。

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