Water Photolysis Research Articles

Significant role of secondary electrons in the formation of a multi-body chemical species spur produced by water radiolysis.

Scientific insights into water photolysis and radiolysis are essential for estimating the direct and indirect effects of deoxyribonucleic acid (DNA) damage. Secondary electrons from radiolysis intricately associated with both effects. In our previous paper, we simulated the femtosecond (1 × 10- 15s) dynamics of secondary electrons ejected by energy depositions of 11-19eV into water via high-energy electron transport using a time-dependent simulation code. The results contribute to the understanding of simple "intra-spur" chemical reactions of tree-body chemical species (hydrated electrons, hydronium ion and OH radical) in subsequent chemical processes. Herein, we simulate the dynamics of the electrons ejected by energy depositions of 20-30eV. The present results contribute to the understanding of complex "inter-spur" chemical reactions of the multi-body chemical species as well as for the formation of complex DNA damage with redox site and strand break on DNA. The simulation results present the earliest formation mechanism of an unclear multi-body chemical species spur when secondary electrons induce further ionisations or electronic excitations. The formation involves electron-water collisions, i.e. ionisation, electronic excitation, molecular excitation and elastic scattering. Our simulation results indicate that (1) most secondary electrons delocalise to ~ 12nm, and multiple collisions are sometimes induced in a water molecule at 22eV deposition energy. (2) The secondary electrons begin to induce diffuse band excitation of water around a few nm from the initial energy deposition site and delocalise to ~ 8nm at deposition energies ~ 25eV. (3) The secondary electron can cause one additional ionisation or electronic excitation at deposition energies > 30eV, forming a multi-body chemical species spur. Thus, we propose that the type and density of chemical species produced by water radiolysis strongly depend on the deposition energy. From our results, we discuss formation of complex DNA damage.

Synthesis of concave Au NRs-Pt-CdS plasmonic photocatalyst with efficient hydrogen production rate

Light-driven water photolysis for hydrogen (H2) generation has been proven to be exceptionally efficient in the field of energy transformation. Nevertheless, the practical applications of many single-component semiconductors still suffer from a relatively low energy conversion efficiency. In this work, concave gold nanorods (Au NRs) with three plasmon resonance modes were synthesized using a one-step method in an aqueous solution. Pt nanoparticles and CdS nanocrystals were rational grown onto Au NRs to design the plasmonic photocatalysts with specific morphology and structure characteristic. Photocatalytic test indicated that concave Au NRs-Pt-CdS hetero-nanostructure possess efficient H2 production rate under visible and near-infrared regions. These findings offer a blueprint for creating a novel group of hetero-nanostructures that combine faceted noble metal nanoparticles with semiconductor materials, demonstrating promise for applications across fields such as photocatalysis and energy storage.

JWST/NIRISS Reveals the Water-rich “Steam World” Atmosphere of GJ 9827 d

With sizable volatile envelopes but smaller radii than the solar system ice giants, sub-Neptunes have been revealed as one of the most common types of planet in the galaxy. While the spectroscopic characterization of larger sub-Neptunes (2.5–4 R ⊕) has revealed hydrogen-dominated atmospheres, smaller sub-Neptunes (1.6–2.5 R ⊕) could either host thin, rapidly evaporating, hydrogen-rich atmospheres or be stable, metal-rich “water worlds” with high mean molecular weight atmospheres and a fundamentally different formation and evolutionary history. Here, we present the 0.6–2.8 μm JWST/NIRISS/SOSS transmission spectrum of GJ 9827 d, the smallest (1.98 R ⊕) warm (T eq,A=0.3 ∼ 620 K) sub-Neptune where atmospheric absorbers have been detected to date. Our two transit observations with NIRISS/SOSS, combined with the existing HST/WFC3 spectrum, enable us to break the clouds–metallicity degeneracy. We detect water in a highly metal-enriched “steam world” atmosphere (O/H of ∼4 by mass and H2O found to be the background gas with a volume mixing ratio of >31%). We further show that these results are robust to stellar contamination through the transit light source effect. We do not detect escaping metastable He, which, combined with previous nondetections of escaping He and H, supports the steam atmosphere scenario. In water-rich atmospheres, hydrogen loss driven by water photolysis happens predominantly in the ionized form, which eludes observational constraints. We also detect several flares in the NIRISS/SOSS light curves with far-UV energies of the order of 1030 erg, highlighting the active nature of the star. Further atmospheric characterization of GJ 9827 d probing carbon or sulfur species could reveal the origin of its high metal enrichment.

In Situ X-ray Absorption Spectroscopy Study of the Deactivation Mechanism of a Ni-SrTiO3 Photocatalyst Slurry Active in Water Splitting.

We used in situ X-ray absorption spectroscopy (XAS) to investigate the composition-performance correlation of Ni-SrTiO3 photocatalysts active for water splitting. After preparation and exposure to ambient conditions, the Ni particles on SrTiO3 consist of Ni(0) and Ni(II) phases, with a 4:1 at % ratio, in a metal/oxide core/shell configuration, as confirmed by XPS and TEM-EDX. In situ XAS experiments using an aqueous slurry of the Ni-SrTiO3 photocatalyst and simultaneous continuous exposure to 365 nm light with a power density of 100 mW cm-2 and the X-rays do not reveal significant changes in oxidation state of the Ni particles. Contrarily, when the X-rays are discontinuously applied, UV excitation leads to oxidation of a significant fraction of Ni(0) to Ni(II), specifically to NiO and Ni(OH)2 phases, along with cocatalyst restructuring. Ni dissolution or oxidation to higher valence states (e.g., Ni(III)) was not observed. The UV light-induced oxidation of Ni(0) causes the hydrogen evolution rate to drop to similar rates as observed for pristine SrTiO3, suggesting that Ni(0) is the active phase for H2 generation. Our results underscore the importance of assessing the effects of (continuous) X-ray exposure to (photo)catalyst-containing aqueous slurries during in situ XAS experiments, which can significantly influence the observation of compositional and structural changes in the (photo)catalysts. We ascribe this to X-ray induced water photolysis and formation of free electrons, which in this study quench SrTiO3 photoholes and prevent Ni oxidation.

Hofmann-type MOF-derived CuNiOx photocathode for effective PEC H2 production

A novel mixed metal oxide of CuNiOx has been successfully obtained via electrosynthesis and thermal conversion of a Hofmann-type MOF Cu(pz)2[Ni(CN)4] (pz = pyrazine). CuNiOx has demonstrated a significant enhancement in light absorption within a visible light range, leading to an impressive increase in photocurrent density and photocatalytic activity during light irradiation compared to CuO. The exceptional photoelectrochemical properties of the photocathodes of CuNiOx have been studied using multiple photoelectrochemical instrumental techniques, which proved the electrodes were stable over the whole water photolysis. The coupling of two metal centers has explained their outstanding performance.

Hydrogen Generation by Photolysis of Water Vis-à-Vis Other Conventional and Advanced Non-conventional Methods of Hydrogen Production—A Review

Hydrogen Generation by Photolysis of Water Vis-à-Vis Other Conventional and Advanced Non-conventional Methods of Hydrogen Production—A Review

Enhanced photocatalytic oxidation of 5-hydroxymethylfurfural using a green bimetallic sulfide catalyst ZnxCd(1-x)S

A novel bimetallic sulfide catalyst, ZnxCd(1-x)S, synthesized via a one-step hydrothermal process, has demonstrated exceptional efficiency in the efficient oxidation of 5-hydroxymethylfurfural (HMF) to 2, 5-dimethylacylfuran (DFF). This transformation is achieved under environmentally benign conditions: without any external oxidant at room temperature and atmospheric pressure, with water as the solvent and visible light. The unique 3D flower-like nanosphere structure of Zn0.4Cd0.6S, characterized by a synergistic composition of ZnS and CdS, facilitates the simultaneous photocatalytic oxidation of water and HMF. The synergistic action of superoxide (∙O2-) and single-linear state oxygen (1O2) served as the main active radicals generated in situ from water photolysis. Remarkably, Zn0.4Cd0.6S exhibited an excellent performance, achieving a remarkable product yield over 50 % and 75 % selectivity after only 3 h. This work presents a sustainable approach to the valorization of HMF and advances the field of photocatalysis without reliance on additional oxidants.

Device for hydrogen production from water photolysis and method therefor

Device for hydrogen production from water photolysis and method therefor

Rapid oxygen isotopic exchange between bicarbonate and water during photosynthesis

Whether rapid oxygen isotopic exchange between bicarbonate and water occurs in photosynthesis is the key to determine the source of oxygen by classic 18O-labeled photosynthetic oxygen evolution experiments. Here we show that both Microcystis aeruginosa and Chlamydomonas reinhardtii utilize a significant proportion (>16%) of added bicarbonate as a carbon source for photosynthesis. However, oxygen isotopic signal in added bicarbonate cannot be traced in the oxygen in organic matter synthesized by these photosynthetic organisms. This contradicts the current photosynthesis theory, which states that photosynthetic oxygen evolution comes only from water, and oxygen in photosynthetic organic matter comes only from carbon dioxide. We conclude that the photosynthetic organisms undergo rapid exchange of oxygen isotope between bicarbonate and water during photosynthesis. At the same time, this study also provides isotopic evidence for a new mechanism that half of the oxygen in photosynthetic oxygen evolution comes from bicarbonate photolysis and half comes from water photolysis, which provides a new explanation for the bicarbonate effect, and suggests that the Kok-Joliot cycle of photosynthetic oxygen evolution, must be modified to include a molecule of bicarbonate in addition to one molecule of water which in turn must be incorporated into the cycle instead of two water molecules. Furthermore, this study provides a theoretical basis for constructing a newer artificial photosynthetic reactor coupling light reactions with the dark reactions.

Amphi-Luminescent MoS2 nanostructure for photocatalytic splitting of water and removal of Methylene Blue

Chemical dyes used in the textile industries are one of the major pollutants in water. Methylene blue (MB) is a commonly seen dye that creates hazardous health problems. In this article the photocatalytic degradation of MB by the nanocatalyst MoS2 (Nano-MoS2) and carbon dot (C Dots) incorporated MoS2 (Nano-CD-MoS2) is reported. The photocatalytic degradation of MB is analyzed based on the electron-hole recombination rate of the catalyst. Photoluminescence emission exhibited by the catalyst is used as a key indicator to probe the electron-hole recombination rate. Nano-MoS2 was synthesized hydrothermally at 180 0C for 8 h from ammonium tetra thiomolybdate (ATTM). C Dot was prepared following a green root from ash guard extract which later mixed with Nano-MoS2 and kept in an autoclave at a temperature 140 °C for 4 h to get Nano-CD-MoS2. The photoluminescence (PL) and photocatalytic behavior of Nano-MoS2 and Nano-CD-MoS2 and their application for water splitting and water purification are reported. The incorporation of graphene and artificial C Dot into MoS2 nanostructures are reported to increase the conductivity and active edge sites of MoS2 that enhances the photocatalytic action. Since green C Dots are eco-friendly and easily synthesizable than artificial C Dots, as a novel study, this article investigated the influence of green C Dots on the PL and photocatalytic performance of nanosized MoS2. Nano-MoS2 and Nano-CD-MoS2 exhibited both upconversion and downconversion PL; accordingly the nanostructures were termed as amphi-luminescent. The amphi-luminescence property widens the photon absorption range and hence enhances the catalytic degradation of dyes. Nano-MoS2 which exhibited lesser intensity of amphi-luminescence emission compared to Nano-CD-MoS2 showed better results in degradation of MB. C Dots may bind with the valence band electrons of MoS2, resulting in the reduction of dangling bonds. Dangling bonds can trap photo-induced excitons to hinder the rate of electron-hole recombination. So, fast electron-hole recombination occurs in Nano-CD-MoS2 than Nano-MoS2. Fast electron-hole recombination supports radiative electron-hole recombination while suppresses the non-radiative energy transfer of electrons and causes high PL intensity. However, according to the energy level diagram, Nano-MoS2 with minimal electron-hole recombination rate is more favorable for O2/O2–,.OH/ OH– and.OH/H2O reactions that facilitate MB degradation. Photocatalytic activity of catalysts were confirmed by measuring the photocurrent from a simple custom-made two-electrode water photolysis cell where the nanocatalysts were dispersed in electrolyte. Lead and steel rods were used as electrodes. Multimeter was used to measure current. Nano-MoS2 exhibited better performance with a maximum photocurrent of 141 µA. Influence of green C Dots in energy levels, PL and photocatalysis of MoS2 and mechanisms of PL and degradation of MB are thoroughly investigated in this article.

Application of Chlorophyll Fluorescence Analysis Technique in Studying the Response of Lettuce (Lactuca sativa L.) to Cadmium Stress.

To reveal the impact of cadmium stress on the physiological mechanism of lettuce, simultaneous determination and correlation analyses of chlorophyll content and photosynthetic function were conducted using lettuce seedlings as the research subject. The changes in relative chlorophyll content, rapid chlorophyll fluorescence induction kinetics curve, and related chlorophyll fluorescence parameters of lettuce seedling leaves under cadmium stress were detected and analyzed. Furthermore, a model for estimating relative chlorophyll content was established. The results showed that cadmium stress at 1 mg/kg and 5 mg/kg had a promoting effect on the relative chlorophyll content, while cadmium stress at 10 mg/kg and 20 mg/kg had an inhibitory effect on the relative chlorophyll content. Moreover, with the extension of time, the inhibitory effect became more pronounced. Cadmium stress affects both the donor and acceptor sides of photosystem II in lettuce seedling leaves, damaging the electron transfer chain and reducing energy transfer in the photosynthetic system. It also inhibits water photolysis and decreases electron transfer efficiency, leading to a decline in photosynthesis. However, lettuce seedling leaves can mitigate photosystem II damage caused by cadmium stress through increased thermal dissipation. The model established based on the energy captured by a reaction center for electron transfer can effectively estimate the relative chlorophyll content of leaves. This study demonstrates that chlorophyll fluorescence techniques have great potential in elucidating the physiological mechanism of cadmium stress in lettuce, as well as in achieving synchronized determination and correlation analyses of chlorophyll content and photosynthetic function.

Efficient metal–organic framework-based dual co-catalysts system assist CdS for hydrogen production from photolysis of water

Metal-organic framework materials (MOFs) and their derivatives have been widely used in the field of photocatalytic water decomposition for hydrogen production. In this study, NiS/CdS was initially acquired and subsequently combined with DUT-67 via ultrasound to create a unique ternary photocatalyst NiS/CdS@DUT-67. The rate of hydrogen production for NiS/CdS@DUT-67 is 9618 μmol·g NiS/CdS−1·h−1 for NiS/CdS@DUT-67, which is 32 times and 2.5 times higher than that for CdS and NiS/CdS, respectively. Of particular interest is the fact that even after 50 h of photocatalysis, the hydrogen production rate did not show a significant decrease, demonstrating its excellent stability compared to CdS and NiS/CdS. In this ternary system, NiS and DUT-67 function as dual co-catalysts for CdS, collaborating to enhance charge separation during the photocatalysis. This study presents a clear demonstration of the advantages of utilizing metal–organic framework derivatives (MOF-derivatives) cophotocatalysts and their synergistic effect, resulting in improved photocatalytic activity and stability of semiconductors. This innovative approach provides a new perspective on constructing photocatalytic materials with exceptional performance.

The ultra-low energy barrier for photocatalytic hydrogen evolution by the creation of Z-scheme SnC/PtSe2 heterojunctions: First-principles calculation

In this study, we designed a vertical heterojunction of SnC/PtSe2 to lower the energy barrier for the photocatalytic hydrogen evolution reaction (HER). Through first-principles calculations, we systematically explored the electronic structure properties, band bending, photocatalytic performance, and light absorption. Our results indicate that photo-generated carriers transfer along the Z-path, exhibiting strong reduction ability and effective carrier utilization. The observed electric field and band bending at the interface facilitate the recombination of photo-generated electron-hole pairs between layers. As a result, photo-generated electrons accumulate on SnC, enabling the continuation of the HER. Specifically, the SnC/PtSe2 heterojunction demonstrates a significantly reduced energy barrier of 0.081 eV for the HER. Furthermore, SnC/PtSe2 heterojunctions also greatly enhance the absorption of infrared and visible light. Our findings provide valuable insights for the development of catalysts in hydrogen production through water photolysis.

The effect of activated water on the photosynthetic processes of plants

The article is devoted to the research of the effect of nutrient solutions prepared on the basis of activated water: anolyte and catholyte on glucose synthesis during photosynthesis using the example of seedlings of vegetable crops: Japanese cabbage of the Mizuna variety, peas of the vegetable variety “Zima”, cucumber of the variety “Vsyo putyom”. The research was carried out to determine the mechanism of activated water influence on photosynthesis. As a result, the proposed working hypothesis on the effectiveness of the activated water influence on photosynthetic processes was confirmed. It has been shown that glucose synthesis is closely related to the reduction of absorbed CO2 by NADPH+ and ATP during photophosphorylation, and then their direct participation in this synthesis. It has been established that the increased concentration of hydrogen protons formed during the photolysis of activated water is the reason for the effectiveness of glucose synthesis, and, consequently, productivity. It has been shown that positively charged hydrogen ions H+ involved in photophosphorylation, forming NADPH+, which together with H+ is involved in glucose synthesis, during photolysis of water during photosynthesis have a concentration of ions 3.13·105 times higher in anolyte (534.67·10-4 M/l) than in inactive water (170.67·10-9 M/l), which provides, in comparison with the control, an increase in glucose synthesis by 26.7% for Japanese cabbage of the Mizuna variety; by 39.7% for peas of the vegetable variety “Zima” and by 33.3% for cucumber of the variety “Vsyo Putyom”. At the same time, for plants of vegetable peas “Zima”, an increase in the intensity of growth in the anolyte was noted in comparison with the control by 12.5%.

Two-dimensional ternary pentagonal BCX (X = P, As, and Sb): promising photocatalyst semiconductors for water splitting with strong piezoelectricity.

Seeking high-performance energy conversion materials is one of the most important issues in designing 2D materials. In the framework of density functional theory, we propose a series of ternary monolayers, penta-BCX (X = P, As, and Sb), and systematically investigate their structural stability, mechanical, piezoelectric, and photocatalytic properties. All three materials are semiconductors with a bandgap ranging from 2.56 eV to 3.24 eV, so they could be promising catalysts for the photolysis of water. Penta-BCX exhibits significant piezoelectric properties attributed to their non-centrosymmetric structure and low in-plane Young's modulus, which are expected to efficiently drive photocatalytic water decomposition. Moreover, the bandgap, band edge position, and light absorption of penta-BCX can be modulated by tensile or compressive strain to enhance their photocatalytic performance in the visible light and ultraviolet regions.

Atmospheric Escape From Three Terrestrial Planets in the L 98-59 System

A critically important process affecting the climate evolution and potential habitability of an exoplanet is atmospheric escape, in which high-energy radiation from a star drives the escape of hydrogen atoms and other light elements from a planet’s atmosphere. L 98-59 is a benchmark system for studying such atmospheric processes, with three transiting terrestrial-sized planets receiving Venus-like instellations (4–25 S ⊕) from their M3 host star. We use the VPLanet model to simulate the evolution of the L 98-59 system and the atmospheric escape of its inner three small planets, given different assumed initial water quantities. We find that, regardless of their initial water content, all three planets accumulate significant quantities of oxygen due to efficient water photolysis and hydrogen loss. All three planets also receive enough strong X-ray and extreme-ultraviolet flux to drive rapid water loss, which considerably affects their developing climates and atmospheres. Even in scenarios of low initial water content, our results suggest that the JWST will be sensitive to observations of retained oxygen on the L 98-59 planets in its future scheduled observations, with planets b and c being the most likely targets to possess an extended atmosphere. Our results constrain the atmospheric evolution of these small rocky planets, and they provide context for current and future observations of the L 98-59 system to generalize our understanding of multiterrestrial planet systems.

Two-dimensional direct Z-scheme AlN/GaS-SiP heterojunctions enhance photocatalytic hydrogen production from water: a DFT study.

Photocatalytic water splitting for hydrogen production offers a feasible solution to the problems of energy shortages and environmental pollution. However, its low photocatalytic efficiency limits the application of this technology in real world scenarios. In this study, a two-dimensional AlN/PSi-GaS-I van der Waals heterojunction is constructed and the properties of water photolysis are studied based on first-principles calculations. The results demonstrate that AlN/PSi-GaS-I exhibits exceptional photocatalytic performance with good stability, a narrow bandgap, appropriate band-edge position, a broader light absorption range and efficient separation of photogenerated electron-hole pairs. Moreover, the Gibbs free energies of different intermediates throughout the entire reaction process are calculated based on type-II and Z-scheme reaction mechanisms. By comparing the free energy barriers of the two pathways, it is observed that the Z-scheme reaction pathway has a lower energy barrier. Consequently, it can be concluded that AlN/PSi-GaS-I belongs to the direct Z-scheme heterojunction. These findings suggest that AlN/PSi-GaS-I exhibits an enhanced redox capacity, efficiently driving the water splitting reaction. More excitingly, the AlN/PSi-GaS-I can undergo spontaneous photocatalytic reactions under acidic conditions when provided with adequate optical driving force. This study not only proves that AlN/PSi-GaS-I is a promising high-efficiency photocatalyst for water splitting, but also describes a method for determining direct Z-scheme heterojunctions, which offers theoretical guidance for the design of efficient and stable photocatalysts.

Hydrogen production by water photo-sonolysis: a modal approach to enhance the ultrasonic acoustic field in the solution

Water photo-sonolysis is considered one of the most innovative ways of hydrogen production. Cited by the Italian strategy on hydrogen research as a promising field for innovation research, it consists of the coupling work of solar-light electromagnetic waves and mechanical ultrasonic waves to induce water splitting. Water photolysis requires catalysts to be performed and optimized, whereas ultrasound sonolysis acts independently. In the state of the art, it was experimentally demonstrated that the rates of hydrogen production by sonolysis rise according to resonance peaks of the solution in function of ultrasound wavelength. To enhance the effects of the ultrasound, the resonance of the solution can be geometrically achieved by acoustic modal analysis of a set of possible solution volumes. According to the geometry of the photo-sono reactor at the lab scale, the shape of the tested solution volumes is cylindrical. The modal analysis was led in a Matlab environment considering the cylindrical volume’s geometry and the fluid’s physical properties. To check the reliability of the simulated results, pressure measurements were led at the lab scale on the simulated water volumes by means of a hydrophone at a significant number of points.

3DOM BiOI/TiO2 composites modified by metal Ag with broad spectrum response for photocatalytic degradation and water splitting

In order to improve the photocatalytic performance of TiO2 and expand its absorption range in the visible light region, depositing noble metals, constructing the p-n heterojunction and controlling the morphology were used to modify TiO2. First, the TiO2 photocatalyst with a three-dimensional ordered macroporous structure was prepared by vacuum impregnation combined with calcination, and then the 3DOM Ag/BiOI/TiO2 composites were successfully prepared by the in-situ deposition and photoreduction. The characterization results show that the composites present a large number of open and transparent pore structures. The pore wall is formed by stacking TiO2 nanoparticles, with BiOI and Ag nanoparticles evenly distributed on the surface of the pore wall and in the macroporous framework, which expands the specific surface area of 3DOM TiO2 and provides more active sites for the reaction. The introduction of BiOI and Ag expands the visible light response range and improves the light utilization efficiency. Furthermore, the formation of the Schottky barrier and the internal electric field formed by the p–n heterojunction effectively promotes the interfacial electron transfer and suppress the electron–hole recombination, thereby generating more active species during the photocatalytic process. The experimental results of multi-mode photocatalytic degradation of methyl orange (MO) also show that 3DOM Ag/BiOI/TiO2 photocatalyst has the best photocatalytic degradation activity. In addition, different samples were tested for hydrogen production by photolysis of water under simulated sunlight conditions, and the results show that 3DOM Ag/BiOI/TiO2 has the best hydrogen production ability of photolysis of water. The excellent performance of multi-modal photocatalytic degradation of organic pollution and high photohydrogen production activity in 3DOM Ag/BiOI/TiO2 composites is attributed to the synergistic effect between the introduction of metallic Ag, the unique 3DOM structure, and the p–n heterojunction.

Simultaneous H2 fuel evolution and value-added organic transformation from a one-dimensional noble-metal-free photocatalyst with spatially separated catalytic sites

Replacing the sluggish O2-producing half-reaction with value-added organic oxidations in water photolysis systems is deemed more practical to generate H2 fuels. While loading of dual cocatalysts for both half-reactions onto nanoscale photocatalysts is highly beneficial for photocatalysis, developing such nanomaterials that are low-cost, stable and easy-to-synthesize remains challenging. Here, noble-metal-free CdS-Co3O4-NiSx nanodumbbells with spatially separated half-reaction sites are designed to simultaneously generate H2 and oxidize benzylamine without any sacrificial agent. In this nanoarchitecture, electron-collecting NiSx and hole-collecting Co3O4 are anchored at the tips and sidewall of CdS nanowires, respectively, to lower the proton reduction and benzylamine oxidation energy barriers, respectively, thus establishing a dual-functional photocatalytic redox system. With significantly promoted charge separation and half-reaction kinetics, the nanodumbbells can produce H2 (47 mmol∙g−1∙h−1) ca. 70 times faster than pure CdS, along with simultaneous benzylamine oxidation. Our findings provide a viable one-dimensional photocatalyst design strategy for various coupled half-reactions.