Near-infrared driven photocatalytic hydrogen production from ammonia borane hydrolysis using heterostructure-upconverted nanoparticles†

IF 5 3区 材料科学 Q2 CHEMISTRY, PHYSICAL
Bushra Maryam, Muhammad Asim, Hamna Qayyum, Lun Pan, Ji-Jun Zou and Xianhua Liu
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Abstract

This study presents a novel approach to hydrogen evolution through ammonia borane dehydrogenation, utilizing the unique properties of upconverted nanoparticles (UCNPs) and safe, abundant near-infrared (NIR) light. By converting low-energy 980 nm NIR photons into high-energy visible photons, UCNPs offer a significant enhancement in catalytic activity. The fabrication of polystyrene-incorporated UCNPs (PS@UCNPs) prevents catalyst agglomeration and breakage, resulting in a 35-fold increase in activity compared to bare UCNPs. This increase is due to the high-energy emitted photons providing sufficient energy for hydrogen evolution, thereby reducing catalyst costs and eliminating the need for intermediate catalysts. The study also explores platinum-coated UCNPs (Pt@UCNPs), which increase photon absorption by platinum nanoparticles, significantly boosting photocatalytic performance. Pt@UCNPs demonstrated 25 times higher activity than PS@UCNPs, attributed to the unique properties of Pt nanoparticles. The activation energies for PS@UCNPs and Pt@UCNPs were 27.5 kJ mol−1 and 48.8 kJ mol−1, respectively, highlighting the synergistic effect of UCNPs utilizing NIR light and Pt utilizing visible light. Reaction kinetics indicated that hydrogen evolution rates increased with both catalyst and ammonia borane concentrations under NIR light. Recyclability tests confirmed the superior stability and durability of PS@UCNPs over Pt@UCNPs, with consistent hydrogen evolution rates across five cycles and minimal degradation. These findings position PS@UCNPs as a robust catalyst system with significant potential for long-term applications, contributing to the broader field of photochemical catalysis and inspiring further innovations in renewable energy systems. As materials and technologies continue to evolve, NIR-activated photocatalytic processes are expected to play a crucial role in the transition to a sustainable energy future, significantly impacting renewable energy and green chemistry.

Abstract Image

Abstract Image

利用异质结构上转换纳米粒子在氨硼烷水解过程中进行近红外光催化制氢
本研究利用上转换纳米粒子(UCNPs)的独特性质和安全、丰富的近红外(NIR)光,提出了一种通过氨硼烷脱氢实现氢进化的新方法。通过将低能量的 980 纳米近红外光子转化为高能量的可见光光子,UCNPs 可显著提高催化活性。聚苯乙烯掺杂 UCNPs(PS@UCNPs)的制造可防止催化剂团聚和断裂,从而使催化活性比裸 UCNPs 提高了 35 倍。这种提高是由于高能发射的光子为氢气进化提供了足够的能量,从而降低了催化剂成本,并消除了对中间催化剂的需求。该研究还探讨了铂涂层 UCNPs(Pt@UCNPs),它能增加铂纳米粒子对光子的吸收,从而显著提高光催化性能。Pt@UCNPs 的活性比 PS@UCNPs 高 25 倍,这归功于铂纳米粒子的独特性质。PS@UCNPs 和 Pt@UCNPs 的活化能分别为 27.5 kJ mol-1 和 48.8 kJ mol-1,凸显了利用近红外光的 UCNPs 和利用可见光的 Pt 的协同效应。反应动力学表明,在近红外光下,氢气进化速率随催化剂和硼烷氨浓度的增加而增加。可回收性测试证实,与 Pt@UCNPs 相比,PS@UCNPs 具有更高的稳定性和耐久性,在五个循环中氢进化率保持一致,降解程度极低。这些发现将 PS@UCNPs 定义为具有长期应用潜力的稳健催化剂体系,有助于拓展光化学催化领域,并激发可再生能源系统的进一步创新。随着材料和技术的不断发展,近红外激活的光催化过程有望在向可持续能源未来过渡的过程中发挥关键作用,对可再生能源和绿色化学产生重大影响。
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来源期刊
Sustainable Energy & Fuels
Sustainable Energy & Fuels Energy-Energy Engineering and Power Technology
CiteScore
10.00
自引率
3.60%
发文量
394
期刊介绍: Sustainable Energy & Fuels will publish research that contributes to the development of sustainable energy technologies with a particular emphasis on new and next-generation technologies.
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