Efficient Hole Extraction and *OH Alleviation by Pd Nanoparticles on GaN Nanowires in Seawater for Solar-Driven H2 and H2O2 Generation

Muhammad Salman Nasir, Ying Zhao, Haotian Ye, Tao Wang, Bowen Sheng, Jun Song, Jinglin Li, Ping Wang, Xinqiang Wang, Zhen Huang, Baowen Zhou
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Abstract

Photocatalytic seawater splitting into hydrogen and hydrogen peroxide (2H2O→H2↑ + H2O2) offers an ultimate solution for simultaneously generating green fuel and value-added chemicals by the two most earth-abundant resources i.e., solar energy and natural seawater. In this study, Pd nanoparticles are integrated with one-dimensional gallium nitride nanowires (Pd NPs/GaN NWs) on a silicon wafer to produce H2 and H2O2 from seawater powered by sunlight. In situ spectroscopic characterizations combined with computational investigations reveal that in this nanohybrid, Pd NPs function as an efficient hole extractor and *OH alleviator during photocatalysis. Meanwhile, the chloride ions in seawater facilitate the H2O→ H2 + H2O2 conversion by improving the charge dynamics and lowering the energy barrier of the key *OH self-coupling step over Pd sites in the catalytic system. As a result, the photocatalyst delivers an appreciable hydrogen production rate of 2.5 mmol⋅cm−2⋅h−1 with a light-to-hydrogen (LTH) efficiency of 4.38 % in natural seawater under concentrated light irradiation of 3 W⋅cm−2 without sacrificial agents and external energies. Notably, the water oxidation reaction produces 300 μmol/L of valuable H2O2 over a duration of 2 hours under a light intensity of 3 W/cm2 using a 20 mL water sample, achieving a light-to-chemical efficiency of 0.53 %. The photocatalyst shows excellent stability for up to 60 hours with a considerable turnover number of 1.42×107 moles H2 per mole of Pd. The outdoor test further suggests the great potential for solar-driven seawater splitting into green fuels and chemicals.

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海水中氮化镓纳米线上Pd纳米粒子的高效空穴萃取和*OH缓解
光催化海水分解为氢和过氧化氢(2H2O→H2↑+ H2O2)提供了一种利用太阳能和天然海水这两种地球上最丰富的资源同时生产绿色燃料和增值化学品的终极解决方案。在这项研究中,钯纳米粒子与一维氮化镓纳米线(Pd NPs/GaN NWs)集成在硅片上,从阳光供电的海水中产生H2和H2O2。原位光谱表征结合计算研究表明,在这种纳米杂化物中,Pd - NPs在光催化过程中作为有效的空穴提取剂和*OH缓解剂。同时,海水中的氯离子改善了催化体系中Pd位点上键*OH自偶联步骤的电荷动力学,降低了键*OH自偶联步骤的能垒,促进了H2O→H2 + H2O2的转化。结果表明,在3 W⋅cm−2的光照射下,该光催化剂的产氢速率为2.5 mmol⋅cm−2⋅h−1,光制氢效率为4.38%,无需牺牲剂和外部能量。值得注意的是,使用20 mL水样,在3 W/cm2的光强下,水氧化反应在2小时内产生300 μmol/L有价H2O2,光化学效率为0.53%。光催化剂表现出优异的稳定性长达60小时,每摩尔Pd的转化率为1.42×107摩尔H2。室外试验进一步表明,太阳能驱动的海水分解成绿色燃料和化学物质的巨大潜力。
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来源期刊
Angewandte Chemie
Angewandte Chemie 化学科学, 有机化学, 有机合成
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