Nanostructure designs for effective solar-to-hydrogen conversion

Nanophotonics ◽  
2012 ◽  
Vol 1 (1) ◽  
pp. 31-50 ◽  
Author(s):  
Shaohua Shen ◽  
Samuel S. Mao

AbstractConversion of energy from photons in sunlight to hydrogen through solar splitting of water is an important technology. The rising significance of producing hydrogen from solar light via water splitting has motivated a surge of developing semiconductor solar-active nanostructures as photocatalysts and photoelectrodes. Traditional strategies have been developed to enhance solar light absorption (e.g., ion doping, solid solution, narrow-band-gap semiconductor or dye sensitization) and improve charge separation/transport to prompt surface reaction kinetics (e.g., semiconductor combination, co-catalyst loading, nanostructure design) for better utilizing solar energy. However, the solar-to-hydrogen efficiency is still limited. This article provides an overview of recently demonstrated novel concepts of nanostructure designs for efficient solar hydrogen conversion, which include surface engineering, novel nanostructured heterojunctions, and photonic crystals. Those first results outlined in the main text encouragingly point out the prominence and promise of these new concepts principled for designing high-efficiency electronic and photonic nanostructures that could serve for sustainable solar hydrogen production.

2021 ◽  
Author(s):  
Moritz Kölbach ◽  
Kira Rehfeld ◽  
Matthias May

Hydrogen produced from water using solar energy constitutes a sustainable alternative to fossil fuels, but solar hydrogen is not yet economically competitive. A major question is whether the approach of coupling photovoltaics via the electricity grid to electrolysis is preferential to higher levels of device integration in ‘artificial leaf’ designs. Here, we scrutinise the effects of thermally coupled solar water splitting on device efficiencies and catalyst footprint for sub-freezing ambient temperatures of -20C. These conditions are found for a significant fraction of the year in many world regions. Using a combination of electrochemical experiments and modelling, we demonstrate that thermal coupling broadens the operating window and significantly reduces the required catalyst loading when compared to electrolysis decoupled from photovoltaics. Efficiency benefits differ qualitatively for double- and triple junction solar absorbers, which has implications for the general design of outdoor-located photoelectochemical devices. Similar to high-efficiency photovoltaics that reached technological maturity in space, application cases in polar or alpine climates could support the scale-up of solar hydrogen at the global scale.


2019 ◽  
Vol 7 (44) ◽  
pp. 25650-25656
Author(s):  
Fengting Luo ◽  
Wen Qiao ◽  
Huichao He ◽  
Xiaoyong Xu ◽  
Jingguo Hu ◽  
...  

Hole dynamics engineering over CdSxO NPs to couple HER with UOR against WOR for a solar-driven waste-to-energy solution.


2017 ◽  
Vol 5 (21) ◽  
pp. 10165-10172 ◽  
Author(s):  
Seung Yo Choi ◽  
Chang-Duk Kim ◽  
Dong Suk Han ◽  
Hyunwoong Park

We have for the first time synthesized a high efficiency CuAlO2 film on transparent conducting substrates via electrochemical deposition.


2021 ◽  
Vol 1 (4) ◽  
Author(s):  
Asieh Akhoondi ◽  
Ankush Sharma ◽  
Dinesh Pathak ◽  
Mohammad Yusuf ◽  
Taye B. Demissie ◽  
...  

In recent decades, the use of photocatalysts in the evolution of hydrogen (H2) has received much attention. However, the use of the well-known titanium oxide and another photocatalyst as a base for noble metals is limited due to their major weakness in electron-hole pair separation. The use of cocatalysts can be a good way to overcome this problem and provide better performance for the evolution of hydrogen. In this review, suitable high-efficiency cocatalysts for solar hydrogen production have been thoroughly reviewed. New strategies and solutions were examined in terms of increasing the recombination of charge carriers, designing reactive sites, and enhancing the wavelengths of light absorption. Several new types of cocatalysts based on semiconductors in noble groups and dual metals have been evaluated. It is expected that these photocatalysts will be able to reduce the activation energy of reaction and charge separation. In this regard, the existing views and challenges in the field of photocatalysts are presented. The characteristics of monoatomic photocatalysts are reviewed in this manuscript and the latest advances in this field are summarized. Further, the future trends and upcoming research are also briefly discussed. Finally, this review presents noble metal-based photocatalysts for providing suitable photocatalysts on a larger scale and improving their applicability.


2021 ◽  
Author(s):  
Moritz Kölbach ◽  
Kira Rehfeld ◽  
Matthias May

Hydrogen produced from water using solar energy constitutes a sustainable alternative to fossil fuels, but solar hydrogen is not yet economically competitive. A major question is whether the approach of coupling photovoltaics via the electricity grid to electrolysis is preferential to higher levels of device integration in ‘artificial leaf’ designs. Here, we scrutinise the effects of thermally coupled solar water splitting on device efficiencies and catalyst footprint for sub-freezing ambient temperatures of -20C. These conditions are found for a significant fraction of the year in many world regions. Using a combination of electrochemical experiments and modelling, we demonstrate that thermal coupling broadens the operating window and significantly reduces the required catalyst loading when compared to electrolysis decoupled from photovoltaics. Efficiency benefits differ qualitatively for double- and triple junction solar absorbers, which has implications for the general design of outdoor-located photoelectochemical devices. Similar to high-efficiency photovoltaics that reached technological maturity in space, application cases in polar or alpine climates could support the scale-up of solar hydrogen at the global scale.


Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1357
Author(s):  
Shiyue Qi ◽  
Yahui Miao ◽  
Ji Chen ◽  
Huichao Chu ◽  
Bingyang Tian ◽  
...  

The development of visible-light-responsive photocatalysts with high efficiency, stability, and eco-friendly nature is beneficial to the large-scale application of solar hydrogen production. In this work, the production of biosynthetic ternary ZnCdS photocatalysts (Eg = 2.35–2.72 eV) by sulfate-reducing bacteria (SRB) under mild conditions was carried out for the first time. The huge amount of biogenic S2− and inherent extracellular proteins (EPs) secreted by SRB are important components of rapid extracellular biosynthesis. The ternary ZnCdS QDs at different molar ratios of Zn2+and Cd2+ from 15:1 to 1:1 were monodisperse spheres with good crystallinity and average crystallite size of 6.12 nm, independent of the molar ratio of Cd2+ to Zn2+. All the ZnCdS QDs had remarkable photocatalytic activity and stability for hydrogen evolution under visible light, without noble metal cocatalysts. Especially, ZnCdS QDs at Zn/Cd = 3:1 showed the highest H2 production activity of 3.752 mmol·h−1·g−1. This excellent performance was due to the high absorption of visible light, the high specific surface area, and the lower recombination rate between photoexcited electrons and holes. The adhered inherent EPs on the ZnCdS QDs slowed down the photocorrosion and improved the stability in photocatalytic hydrogen evolution. This study provides a new direction for solar hydrogen production.


Sign in / Sign up

Export Citation Format

Share Document