The bacterial phytopathogen Xanthomonas campestris pv. campestris (Xcc) relies on the hrp (hypersensitive response and pathogenicity) genes to cause disease and induce hypersensitive response (HR). The hrp genes of bacterial phytopathogens are divided into two groups. Xcc hrp genes belong to group II. It has long been known that the group II hrp genes are activated by an AraC-type transcriptional regulator whose expression is controlled by a two-component system (TCS) response regulator (named HrpG in Xcc). However, no cognate sensor kinase has yet been identified. Here, we present evidence showing that the Xcc open-reading frame XC_3670 encodes a TCS sensor kinase (named HpaS). Mutation of hpaS almost completely abolished the HR induction and virulence. Bacterial two-hybrid and protein pull-down assays revealed that HpaS physically interacted with HrpG. Phos-tag™ SDS-PAGE analysis showed that mutation in hpaS reduced markedly the phosphorylation of HrpG in vivo. These data suggest that HpaS and HrpG are most likely to form a TCS. We also showed that XC_3669 (named hpaR2), which is adjacent to hpaS and encodes a putative TCS response regulator, is required for full virulence but not HR induction. HpaR2 also physically interacted with HpaS, suggesting that HpaS may also form another TCS with HpaR2.

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The oxygen evolution reaction (OER) in water splitting plays a critical role in some clean energy production systems. Transition-metal oxides as one of the most common OER electrocatalysts have been widely explored; however, their activity is limited by low electrical conductivity, slow mass transfer, and inadequate active sites. Herein, we develop a feasible strategy in which layered twodimensional metal−organic frameworks (2D MOFs) act as templates to construct metal oxide/carbon (MO x /C, M = Co, Ni, and Cu) nanosheet arrays for the OER. Because of improved conductivity and more exposed active sites afforded by their 2D structures with rich hierarchical pores and the incorporation with porous carbon, these 2D MOF-derived MO x /C arrays present high electrocatalytic activities and good durability. Particularly, Co 3 O 4 /C BDC , NiO/C BDC , and Cu 2 O/ S−C TDC exhibit low overpotentials of 208, 285, and 313 mV at the current density of 10 mA cm −2 , respectively, outperforming all previously reported corresponding metal oxide-based catalysts.

Hydrogen spillover (HSo) has emerged to upgrade the hydrogen evolution reaction (HER) activity of Pt‐support electrocatalysts, but it is not applicable to the deprotonated oxygen evolution reaction (OER). Non‐precious catalysts that can perform well in both HSo and deprotonation (DeP) are extremely desirable for a sustainable hydrogen economy. Herein, an affordable MoS2/NiPS3 vertical heterostructure catalyst is presented to synergize HSo and DeP for efficient water electrolysis. The internal polarization field (IPF) is clarified as the driving force of HSo in HER electrocatalysis. The HSo from the MoS2 edge to NiPS3 can activate the NiPS3 basal plane to boost the HER activity of the MoS2/NiPS3 heterostructure (112 mV vs reversible hydrogen electrode (RHE) at 10 mA cm–2), while for OER, the IPF in the heterostructure can facilitate the hydroxyl diffusion and render MoS2‐to‐NiPS3/P‐to‐S dual‐pathways for DeP. As a result, the stacking of OER‐inactive MoS2 on the NiPS3 surface still brings intriguing OER enhancements. With them serving as electrode couples, the overall water splitting is attested stably with a cell voltage of 1.64 V at 10 mA cm−2. This research puts forward the IPF as the criterion in the rational design of HSo/DeP‐unified non‐precious catalysts for efficient water electrolysis.

The reverse water-gas shift reaction (RWGSR), a crucial stage in the conversion of abundant CO 2 into chemicals or hydrocarbon fuels, has attracted extensive attention as a renewable system to synthesize fuels by non-traditional routes. There have been persistent efforts to synthesize catalysts for industrial applications, with attention given to the catalytic activity, CO selectivity, and thermal stability. In this review, we describe the thermodynamics, kinetics, and atomic-level mechanisms of the RWGSR in relation to efficient RWGSR catalysts consisting of supported catalysts and oxide catalysts. In addition, we rationally classify, summarize, and analyze the effects of physicochemical properties, such as the morphologies, compositions, promoting abilities, and presence of strong metal-support interactions (SMSI), on the catalytic performance and CO selectivity in the RWGSR over supported catalysts. Regarding oxide catalysts (i.e., pure oxides, spinel, solid solution, and perovskite-type oxides), we emphasize the relationships among their surface structure, oxygen storage capacity (OSC), and catalytic performance in the RWGSR. Furthermore, the abilities of perovskite-type oxides to enhance the RWGSR with chemical looping cycles (RWGSR-CL) are systematically illustrated. These systematic introductions shed light on development of catalysts with high performance in RWGSR.