Gobbato Thomas, Volpato Giulia Alice, Sartorel Andrea, Bonchio Marcella
Department of Chemical Sciences, University of Padova via Marzolo 1 35131 Padova Italy
ITM-CNR Section of Padova, INSTM Unit of Padova via Marzolo 1 35131 Padova Italy.
Chem Sci. 2023 Oct 4;14(44):12402-12429. doi: 10.1039/d3sc03780k. eCollection 2023 Nov 15.
The conversion of light into chemical energy is the game-changer enabling technology for the energetic transition to renewable and clean solar fuels. The photochemistry of interest includes the overall reductive/oxidative splitting of water into hydrogen and oxygen and alternatives based on the reductive conversion of carbon dioxide or nitrogen, as primary sources of energy-rich products. Devices capable of performing such transformations are based on the integration of three sequential core functions: light absorption, photo-induced charge separation, and the photo-activated breaking/making of molecular bonds specific catalytic routes. The key to success does not rely simply on the individual components' performance, but on their optimized integration in terms of type, number, geometry, spacing, and linkers dictating the photosynthetic architecture. Natural photosynthesis has evolved along this concept, by integrating each functional component in one specialized "body" (from the Greek word "soma") to enable the conversion of light quanta with high efficiency. Therefore, the natural "quantasome" represents the key paradigm to inspire man-made constructs for artificial photosynthesis. The case study presented in this perspective article deals with the design of artificial photosynthetic systems for water oxidation and oxygen production, engineered as molecular architectures then rendered on electrodic surfaces. Water oxidation to oxygen is indeed the pervasive oxidative reaction used by photosynthetic organisms, as the source of reducing equivalents (electrons and protons) to be delivered for the processing of high-energy products. Considering the vast and abundant supply of water (including seawater) as a renewable source on our planet, this is also a very appealing option for photosynthetic energy devices. We will showcase the progress in the last 15 years (2009-2023) in the strategies for integrating functional building blocks as molecular photosensitizers, multi-redox water oxidation catalysts and semiconductor materials, highlighting how additional components such as redox mediators, hydrophilic/hydrophobic pendants, and protective layers can impact on the overall photosynthetic performance. Emerging directions consider the modular tuning of the multi-component device, in order to target a diversity of photocatalytic oxidations, expanding the scope of the primary electron and proton sources while enhancing the added-value of the oxidation product beyond oxygen: the selective photooxidation of organics combines the green chemistry vision with renewable energy schemes and is expected to explode in coming years.
将光能转化为化学能是推动向可再生和清洁太阳能燃料进行能源转型的变革性技术。相关的光化学过程包括将水整体还原/氧化分解为氢气和氧气,以及基于二氧化碳或氮气还原转化的替代方案,这些是富含能量产品的主要来源。能够进行此类转化的装置基于三个连续核心功能的整合:光吸收、光致电荷分离以及光激活分子键的断裂/形成特定催化途径。成功的关键不仅仅取决于各个组件的性能,还在于它们在类型、数量、几何形状、间距以及决定光合结构的连接体方面的优化整合。自然光合作用就是沿着这一概念发展而来的,通过将每个功能组件整合到一个专门的“体”(源自希腊语“soma”)中,以实现高效的光量子转化。因此,天然的“量子体”代表了启发人工光合作用人造结构的关键范例。这篇观点文章中呈现的案例研究涉及用于水氧化和氧气生成的人工光合系统的设计,该系统被设计为分子结构,然后呈现在电极表面。水氧化生成氧气确实是光合生物所使用的普遍氧化反应,它是为处理高能产物而输送还原当量(电子和质子)的来源。考虑到地球上水(包括海水)作为可再生资源的巨大且丰富的供应,这对于光合能量装置来说也是一个非常有吸引力的选择。我们将展示过去15年(2009 - 2023年)在将功能性构建块整合为分子光敏剂、多氧化还原水氧化催化剂和半导体材料的策略方面取得的进展,突出氧化还原介质、亲水性/疏水性侧链和保护层等附加组件如何影响整体光合性能。新兴方向考虑对多组件装置进行模块化调整,以针对多种光催化氧化反应,扩大初级电子和质子源的范围,同时提高氧化产物(超越氧气)的附加值:有机化合物的选择性光氧化将绿色化学愿景与可再生能源方案相结合,预计在未来几年会蓬勃发展。