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Precisely regulating surface reconstruction of copper (Cu) chalcogenides‐based catalysts to promote the multicarbon (C2+)selectivity of the electrochemical CO2 reduction reaction (CO2RR) is hampered by the challenging control of the intractable anions and the optimal Cuδ+ reduction (0 < δ < 1). Herein, a porous carbon‐supported copper selenides electrocatalyst that can remarkably improve the C2‐product yield and especially unveil the time‐revolved electrochemical CO2RR reconstruction process to enable the high C2‐selectivity, most notably for ethanol is constructed. The Faradic efficiency (FE) of C2‐products achieved is as high as ≈85.2% with a partial current density of 229.5 mA cm−2. Operando infrared spectroscopy and density functional theory (DFT) calculations unravel that the surface Se vacancies (VSe) formation brings closer the neighboring Cu+ atoms and activates the Cu sites, thereby rendering efficient generation of the key intermediates (*CO and *CHO) and lowering the C–C coupling barrier for C2 production. The appearance of metallic Cu can shorten the next‐nearest Cu0–Cu+ distance for O atom to bridge in, leading to the preferential formation of *OC2H4 towards ethanol instead of C–O bond cleavage to form ethylene. This work opens the avenue of designing suitable local atomic structures catalysts to engage the intermediates for targeted CO2RR products. [ABSTRACT FROM AUTHOR]

Post‐treatment is a widely used strategy to reduce defects in perovskite films, but has been largely limited to the solution phase. Herein, the posttreatment tool kit and develop a universal amine salts (AIXI) vapor healing strategy by taking advantage of the penetrating power of vapor and the soft‐matter characteristics of halide perovskite is expanded. In a striking demonstration, the post‐treatment of pristine perovskite layers allows simultaneous filling of the MA+ and I– vacancies, passivation of both the cation and anion defects, and healing of the films to high order and high crystallinity required for high device performance, from the surface to the bulk and all the way down to the bottom. Experiments and DFT calculations revealed that charge extraction can be enhanced and non‐radiative recombination can be reduced by regulating the energy levels and reducing the trap states via the AIXI vapor healing. Moreover, the diffusing AIXI can reach the NiOx surface to obstruct the undesirable interfacial reactions and passivate the interface defects, further reducing the open‐circuit voltage (Voc) loss. The vapor healing strategy substantially reduces the trap density from 4.76 × 1015 to 1.04 × 1015 cm–3, and promots power conversion efficiency of the champion device from 17.92% to 20.48% with superior device consistency, Voc up to 1.114 V and the operational device stability. [ABSTRACT FROM AUTHOR]

As a prerequisite for a sustainable energy economy in the future, designing earth‐abundant MoS2 catalysts with a comparable hydrogen evolution catalytic performance in both acidic and alkaline environments is still an urgent challenge. Decreasing the energy barriers could enhance the catalysts' activity but is not often a strategy for doing so. Here, the first kinetic‐oriented design of the MoS2‐based heterostructure is presented for pH‐universal hydrogen evolution catalysis by optimizing the electronic structure based on the simultaneous modulation of the 3d‐band‐offsets of Ni, Co, and Mo near the interface. Benefiting from this desirable electronic structure, the obtained MoS2/CoNi2S4 catalyst achieves an ultralow overpotential of 78 and 81 mV at 10 mA cm−2, and turnover frequency as high as 2.7 and 1.7 s−1 at the overpotential of 200 mV in alkaline and acidic media, respectively. The MoS2/CoNi2S4 catalyst represents one of the best hydrogen evolution reaction performing ones among MoS2‐based catalysts reported to date in both alkaline and acidic environments, and equally important is the remarkable long‐term stability with negligible activity loss after maintaining at 10 mA cm−2 for 48 h in both acid and base. This work highlights the potential to deeply understand and rationally design highly efficient pH‐universal electrocatalysts for future energy storage and delivery. [ABSTRACT FROM AUTHOR]

Trap states in semiconductors usually degrade charge separation and collection in photovoltaics due to trap-mediated nonradiative recombination. Here, it is found that perovskite can be heavily doped in low concentration with non-ignorable broadband infrared absorption in thick films and their trap states accumulate electrons through infrared excitation and hot carrier cooling. A hybrid one-sided abrupt perovskite/TiO2 p-N heterojunction is demonstrated that enables partial collection of these trap-filled charges through a tunneling process instead of detrimental recombination. The tunneling is from broadband trap states in the wide depleted p-type perovskite, across the barrier of the narrow depleted TiO2 region (<5 nm), to the N-type TiO2 electrode. The trap states inject carriers into TiO2 through tunneling and produce around-unity peak external quantum efficiency, giving rise to near-infrared photovoltaics. The near-infrared response allows photodetecting devices to work in both diode and conductor modes. This work opens a new avenue to explore the near-infrared application of hybrid perovskites. [ABSTRACT FROM AUTHOR]

Halide perovskites are reputed as highly promising photoelectronic materials for direct X‐ray detectors, but realizing large‐area flat‐panel imaging requires to address the compatibility issue of the electronic, surficial, and mechanical properties between the perovskite and the readout circuit board. Here, a low‐dimensional MA3Bi2I9 perovskite is chosen to achieve a good match in a balancing act between the two by exploiting an orientation control strategy for perovskite film growth. The most striking consequence of the orientation controlled growth is the excellent adhesion of the thick perovskite film to the electronic board in large area and effectively addresses the charge sharing effect, which has been notoriously difficult to achieve. The resulting detector, exhibits an X‐ray imaging area of 2.8 × 3.2 cm, with a spatial resolution of 4.0 lp mm⁻¹, the highest yet achieved for polycrystalline perovskite detectors based on TFT backplanes, and a sensitivity of 588 µCGyair−1 cm−2 while maintaining a dark current below 10 nA cm⁻2, this is also the highest value recorded to date for polycrystalline zero‐dimensional perovskite detectors. This device clearly revealing the intricate internal structures of both biological specimens and industrial products. This outcome demonstrates the potential of zero‐dimensional perovskites in X‐ray planar imaging and highlights the critical role of orientation control strategies. [ABSTRACT FROM AUTHOR]

The organic–inorganic halide CH3NH3PbI3 (MAPbI3) has been the most commonly used light absorber layer of perovskite solar cells (PSCs); however, solution‐processed MAPbI3 films usually suffer from random crystal orientation and high trap density, resulting in inferior power conversion efficiency (PCE) with open circuit voltage (Voc) being typically below 1.2 V for PSC devices. Herein, for the first time an imidazole sulfonate zwitterion, 4‐(1H‐imidazol‐3‐ium‐3‐yl)butane‐1‐sulfonate (IMS), is applied as a bifunctional additive in regular‐structure planar heterojunction PSC devices to regulate the crystal orientation, yielding highly ordered MAPbI3 film and passivating the trap states of the film. Such a dual effect of IMS is fulfilled via coordination interactions between the sulfonate moiety of IMS with the Pb2+ ion and the electrostatic interaction between the imidazole of IMS with the I– ion of MAPbI3. As a result, under a optimized IMS doping ratio of 0.5 wt%, the PSC device exhibits a significant increase in PCE from 18.77% to 20.84%, with suppressed current–voltage hysteresis and promoted ambient stability. Moreover, a high Voc of 1.208 V is achieved under a higher IMS doping ratio of 1.2 wt%, which is the highest Voc for regular‐structure MAPbI3 planar PSC devices based on TiO2 electron transport layer. [ABSTRACT FROM AUTHOR]

The hole transport material (HTM) free carbon based perovskite solar cells (C‐PSCs) are promising for its manufactural simplicity, but they currently suffer from low power conversion efficiencies (PCE) largely because of the voltage loss. Here, a new strategy to increase the PCE by incorporating an ultrathin ferroelectric oxide PbTiO3 layer between the electron transport material and the halide perovskite is reported. The resulting C‐PSCs have achieved PCEs up to 16.37%, which is the highest record for HTM‐free C‐PSCs to date, mainly ascribable to the ferroelectric layer enhanced open circuit voltage. Detail measurements and analysis show an enhanced built‐in potential in the C‐PSCs as well as suppression of the non‐radiative recombination due to the ferroelectric PbTiO3 layer incorporation, accounting for the boosted VOC and photovoltaic performance. An ultrathin ferroelectric oxide PbTiO3 layer is incorporated between the electron transport material and the halide perovskite in the hole transport material (HTM) free carbon‐based perovskite solar cell (C‐PSCs). The achieved power conversion efficiency is as high as 16.37%, which is the highest record for HTM‐free C‐PSCs to date, mainly ascribable to the ferroelectric layer enhanced open circuit voltage. [ABSTRACT FROM AUTHOR]

This document is a correction to a scientific article titled "Enzyme-Mediated Tumor Starvation and Phototherapy Enhance Mild-Temperature Photothermal Therapy." The correction addresses two mistakes found in Figure 3e and Figure 4g of the article. The errors were related to duplicate areas in the images and mislabeling of pictures during the image typesetting process. The correction does not impact the conclusions of the paper. The authors apologize for any inconvenience caused and provide the corrected figures in the document. [Extracted from the article]